Nickel-catalyzed synthesis of five-membered heterocycles

References

• (a) Balaban, A. T.; Oniciu, D. C.; Katritzky, A. R. Aromaticity as a Cornerstone of Heterocyclic Chemistry. Chem. Rev. 2004, 104, 2777. DOI: 10.1021/cr0306790.
   PubMed Web of Science ®Google Scholar
  (b) Majumdar, P.; Pati, A.; Patra, M.; Behera, R. K.; Behera, A. K. Acid Hydrazides, Potent Reagents for Synthesis of Oxygen-, Nitrogen-, and/or Sulfur-Containing Heterocyclic Rings. Chem. Rev. 2014, 114, 2942. DOI: 10.1021/cr300122t.
   PubMed Web of Science ®Google Scholar
  (c) Reddy, C. R.; Ranjan, R.; Kumaraswamy, P.; Reddy, M. D.; Grée, R. 1-Aryl Propargylic Alcohols as Handy Synthons for the Construction of Heterocycles and Carbocycles. COC. 2014, 18, 2603. DOI: 10.2174/138527281820141028104907.
   Web of Science ®Google Scholar
  (d) Uredi, D.; Reddy, M. D.; Watkins, E. B. A Unified Strategy for the Synthesis of β-Carbolines, γ-Carbolines, and Other Fused Azaheteroaromatics under Mild, Metal-Free Conditions. Org. Lett. 2018, 20, 6336. DOI: 10.1021/acs.orglett.8b02441.
   PubMed Web of Science ®Google Scholar
  (e) Reddy, M. D.; Fronczek, F. R.; Watkins, E. B. Rh-Catalyzed, Regioselective, C–H Bond Functionalization: Access to Quinoline-Branched Amines and Dimers. Org. Lett. 2016, 18, 5620. DOI: 10.1021/acs.orglett.6b02848.
   PubMed Web of Science ®Google Scholar
  (f) Nagesh, N.; Raju, G.; Srinivas, R.; Ramesh, P.; Reddy, M. D.; Reddy, C. R. A Dihydroindolizino Indole Derivative Selectively Stabilizes G-Quadruplex DNA and down-Regulates c-MYC Expression in Human Cancer Cells. Biochimica Biophysica Acta. 2015, 1850, 129. DOI: 10.1016/j.bbagen.2014.10.004.;
   PubMed Web of Science ®Google Scholar
  (g) Reddy, M. D.; Kobori, H.; Mori, T.; Wu, J.; Kawagishi, H.; Watkins, E. B. Gram-Scale, Stereoselective Synthesis and Biological Evaluation of (+)-Armillariol C. J. Nat. Prod. 2017, 80, 2561.
   PubMed Web of Science ®Google Scholar
  (h) Das, A.; Kulkarni, A.; Torok, B. Environmentally Benign Synthesis of Heterocyclic Compounds by Combined Microwave-Assisted Heterogeneous Catalytic Approaches Green Chem 2012, 14, 17. DOI: 10.1039/C1GC15837F.
   Web of Science ®Google Scholar
• (a) Martins, M.; Cunico, W.; Pereira, C.; Sinhorin, A.; Flores, A.; Bonacorso, H.; Zanatta, N. 4-Alkoxy-1,1,1-Trichloro-3-Alken-2-Ones: Preparation and Applications in Heterocyclic Synthesis. Curr. Org. Synth. 2004, 1, 391. DOI: 10.2174/1570179043366611.
   Web of Science ®Google Scholar
  (b) Liu, Q.; Wu, L.; Jackstell, R.; Beller, M. Using carbon dioxide as a building block in organic synthesis. Nature Commun. 2015, 6, 5933.
   PubMed Web of Science ®Google Scholar
  (c) Kaur, N. Palladium-Catalyzed Approach to the Synthesis of S -Heterocycles. Catal. Rev. 2015, 57, 478.
   Web of Science ®Google Scholar
  (d) Kaur, N. Mercury-Catalyzed Synthesis of Heterocycles. Synth. Commun. 2018, 48, 2715. DOI: 10.1080/00397911.2018.1497657.
   Web of Science ®Google Scholar
  (e) Kaur, N. Photochemical Irradiation: Seven and Higher Membered O -Heterocycles. Synth. Commun. 2018, 48, 2935. DOI: 10.1080/00397911.2018.1514051.
   Web of Science ®Google Scholar
  (f) Kaur, N. Synthesis of Seven and Higher Membered Nitrogen Containing Heterocycles using Photochemical Irradiation Synth. Commun. 2018, 48, 2815. DOI: 10.1080/00397911.2018.1501488.
   Web of Science ®Google Scholar
• (a) Domling, A. Recent developments in isocyanide based multi-component reactions in applied chemistry. Chem. Rev. 2006, 106, 17.
   PubMed Web of Science ®Google Scholar
  (b) Reddy, C. R.; Valleti, R. R.; Reddy, M. D. A Thioannulation Approach to Substituted Thiophenes from Morita-Baylis-Hillman Acetates of Acetylenic aldehydes. J. Org. Chem. 2013, 78, 6495. DOI: 10.1021/jo400567h.
   PubMed Web of Science ®Google Scholar
  (c) Reddy, C. R.; Dilipkumar, U.; Reddy, M. D. Novel [4 + 2]-Benzannulation to Access Substituted Benzenes and Polycyclic Aromatic and Benzene-Fused Heteroaromatic Compounds. Org. Lett. 2014, 16, 3792. DOI: 10.1021/ol501683v.
   PubMed Web of Science ®Google Scholar
  (d) Reddy, C. R.; Panda, S. A.; Reddy, M. D. Aza-Annulation of Enynyl Azides: A New Approach to Substituted Pyridines. Org. Lett. 2015, 17, 896. DOI: 10.1021/ol503752k.
   PubMed Web of Science ®Google Scholar
  (e)Venkateshwarlu, R.; Chinnababu, B.; Ramulu, U.; Purushotham Reddy, K.; Damoder Reddy, M.; Sowjanya, P.; Venkateswara Rao, P.; Aravind, S. Synthesis and Biological Evaluation of (-)-Kunstleramide and its Derivatives. Medchemcomm. 2017, 8, 394. DOI: 10.1039/c6md00606j.
   PubMed Web of Science ®Google Scholar
  (f) Reddy, C. R.; Reddy, M. D.; Srikanth, B.; Prasad, K. R. Morita-Baylis-Hillman Acetates of Acetylenic Aldehydes: Versatile Synthons for Substituted Pyrroles via a Metal-Free Tandem Reaction. Org. Biomol. Chem. 2011, 9, 6027. DOI: 10.1039/c1ob05402c.
   PubMed Web of Science ®Google Scholar
• (a) Kaur, N. J. Benign Approaches for the Microwave-Assisted Synthesis of Five-Membered 1,2- N, N -Heterocycles. J. Heterocyclic Chem. 2015, 52, 953.
   Web of Science ®Google Scholar
  (b) Kaur, N. Methods for Metal and Non-Metal Catalyzed Synthesis of Six-Membered Oxygen Containing Poly-Heterocycles. COS 2017, 14, 531. DOI: 10.2174/1570179413666161021104941.
   Web of Science ®Google Scholar
  (c) Kaur, N. Photochemical reactions: synthesis of six-membered N-heterocycles. Curr. Org. Synth. 2017, 14, 972.
   Web of Science ®Google Scholar
  (d) Kaur, N. Ionic Liquids: Promising but Challenging Solvents for the Synthesis of NHeterocycles. Mroc. 2017, 14, 3. DOI: 10.2174/1570193X13666161019120050.
   Web of Science ®Google Scholar
  (e) Kaur, N. Metal Catalysts for the Formation of Six-Membered N -Polyheterocycles. Synth. React. Inorg. Met. Org. Nano-Met. Chem. 2016, 46, 983. DOI: 10.1080/15533174.2014.989620.
   Web of Science ®Google Scholar
  (f) Kaur, N. Applications of Gold Catalysts for the Synthesis of Five-Membered O -Heterocycles. Inorg. Nano-Met. Chem. 2017, 47, 163. DOI: 10.1080/15533174.2015.1068809.
   Web of Science ®Google Scholar
  (g) Orru, R. V. A.; de Greef, M. Recent Advances in Solution-Phase Multicomponent Methodology for the Synthesis of Heterocyclic Compounds. Synthesis 2003, 10, 1471. DOI: 10.1055/s-2003-40507.
   Web of Science ®Google Scholar
  (h) Kaur, N. Ruthenium Catalysis in Six-Membered O -Heterocycles Synthesis. Synth. Commun. 2018, 48, 1551. DOI: 10.1080/00397911.2018.1457698.
   Web of Science ®Google Scholar
  (i) Kaur, N. Green Synthesis of Three- to Five-Membered O -Heterocycles Using Ionic Liquids. Synth. Commun. 2018, 48, 1588. DOI: 10.1080/00397911.2018.1458243.
   Web of Science ®Google Scholar
  (j) Kaur, N. Ultrasound-Assisted Green Synthesis of Five-Membered O- and S- Heterocycles. Synth. Commun. 2018, 48, 1715. DOI: 10.1080/00397911.2018.1460671.
   Web of Science ®Google Scholar
  (k) Kaur, N. Photochemical Mediated Reactions in Five-Membered O- Heterocycles Synthesis. Synth. Commun. 2018, 48, 2119. DOI: 10.1080/00397911.2018.1485165.
   Web of Science ®Google Scholar
  (l) Kaur, N. Ruthenium Catalyzed Synthesis of Five-Membered O‑Heterocycles. Inorg. Chem. Commun. 2019, 99, 82.
   Web of Science ®Google Scholar
  (m) Reddy, C. R.; Reddy, M. D.; Dilipkumar, U. Total Synthesis of a Pyrrole Lactone Alkaloid, Longanlactone. Eur. J. Org. Chem. 2014, 28, 6310. DOI: 10.1002/ejoc.201402563.
   Web of Science ®Google Scholar
  (n) Reddy, C. R.; Rao, N. N.; Reddy, M. D. Total Synthesis of (+)‐Seimatopolide A. Eur. J. Org. Chem. 2012, 26, 4910. DOI: 10.1002/ejoc.201200732.
   Web of Science ®Google Scholar
  (o) Tasker, S. Z.; Standley, E. A.; Jamison, T. F. Recent Advances in Homogeneous Nickel Catalysis. Nature 2014, 509, 299. DOI: 10.1038/nature13274.
   PubMed Web of Science ®Google Scholar
• (a) Kaur, N. Palladium-Catalyzed Approach to the Synthesis of Five-Membered O-Heterocycles. Inorg. Chem. Commun. 2014, 49, 86. DOI: 10.1016/j.inoche.2014.09.024.
   Web of Science ®Google Scholar
  (b) Kaur, N.; Kishore, D. Nitrogen-Containing Six-Membered Heterocycles: Solid-Phase Synthesis. Synth. Commun. 2014, 44, 1173. DOI: 10.1080/00397911.2012.760129.
   Web of Science ®Google Scholar
  (c) Kaur, N.; Kishore, D. Solid-Phase Synthetic Approach toward the Synthesis of Oxygen-Containing Heterocycles. Synth. Commun. 2014, 44, 1019. DOI: 10.1080/00397911.2012.760131.
   Web of Science ®Google Scholar
  (d) Kaur, N. Microwave-Assisted Synthesis of Five-Membered O-Heterocycles. Synth. Commun. 2014, 44, 3483. DOI: 10.1080/00397911.2013.800213.
   Web of Science ®Google Scholar
  (e) Kaur, N. Microwave-Assisted Synthesis of Five-Membered O,N-Heterocycles. Synth. Commun. 2014, 44, 3509. DOI: 10.1080/00397911.2013.800214.
   Web of Science ®Google Scholar
  (f) Kaur, N. Microwave-Assisted Synthesis of Five-Membered O,N,N-Heterocycles. Synth. Commun. 2014, 44, 3229. DOI: 10.1080/00397911.2013.798666.
   Web of Science ®Google Scholar
  (g) Kaur, N. Synthesis of Six- and Seven-Membered Heterocycles under Ultrasound Irradiation. Synth. Commun. 2018, 48, 1235. DOI: 10.1080/00397911.2018.1434894.
   Web of Science ®Google Scholar
  (h) Kaur, N. Photochemical Reactions as Key Steps in Five-Membered N- Heterocycle Synthesis. N. Synth. Commun. 2018, 48, 1259. DOI: 10.1080/00397911.2018.1443218.
   Web of Science ®Google Scholar
  (i) Kaur, N. Solid-Phase Synthesis of Sulfur Containing Heterocycles. N. J. Sulfur Chem. 2018, 39, 544. DOI: 10.1080/17415993.2018.1457673.
   Web of Science ®Google Scholar
  (j) Reddy, C. R.; Reddy, M. D.; Babu, K. H. Organocatalyzed Intramolecular Michael Addition of Morita–Baylis–Hillman Adducts of β‐Arylnitroethylenes: An Entry to 3‐Aryl‐4‐nitrocyclohexanones. Eur. J. Org. Chem. 2012, 32, 6414. DOI: 10.1002/ejoc.201200884.
   Web of Science ®Google Scholar
  (k) Reddy, M. D.; Watkins, E. B. Palladium-Catalyzed Direct Arylation of C(sp(3))-H Bonds of α-Cyano Aliphatic Amides. J. Org. Chem. 2015, 80, 11447. DOI: 10.1021/acs.joc.5b02138.
   PubMed Web of Science ®Google Scholar
  (l) Ananikov, V. P. Nickel: The “Spirited Horse” of Transition Metal Catalysis. ACS Catal. 2015, 5, 1964. DOI: 10.1021/acscatal.5b00072.
   Web of Science ®Google Scholar
  (m) Shi, S.; Szostak, M. Efficient Synthesis of Diaryl Ketones by Nickel-Catalyzed Negishi Cross-Coupling of Amides by Carbon-Nitrogen Bond Cleavage at Room Temperature Accelerated by a Solvent Effect. Chemistry 2016, 22, 10420. DOI: 10.1002/chem.201602202.
   PubMed Web of Science ®Google Scholar
• (a) Kaur, N. Metal Catalysts: Applications in Higher-Membered N-Heterocycles Synthesis. J. Iran. Chem. Soc. 2015, 12, 9. DOI: 10.1007/s13738-014-0451-5.
   Web of Science ®Google Scholar
  (b) Kaur, N. Insight into Microwave-Assisted Synthesis of Benzo Derivatives of Five-Membered N,N -Heterocycles. Synth. Commun. 2015, 45, 1269.
   Web of Science ®Google Scholar
  (c) Kaur, N. Synthesis of Fused Five-Membered N,N -Heterocycles Using Microwave Irradiation. Synth. Commun. 2015, 45, 1379. DOI: 10.1080/00397911.2013.828078.
   Web of Science ®Google Scholar
  (d) Kaur, N. Microwave-Assisted Synthesis of Seven-Membered S -Heterocycles. Synth. Commun. 2014, 44, 3201. DOI: 10.1080/00397911.2013.798665.
   Web of Science ®Google Scholar
  (e) Kaur, N. Six-Membered N -Heterocycles: Microwave-Assisted Synthesis. IJCA. 2015, 45, 1. DOI: 10.5120/21644-4985.
   Google Scholar
  (f) Kaur, N. Polycyclic Six-Membered N -Heterocycles: Microwave-Assisted Synthesis. Synth. Commun. 2015, 45, 35. DOI: 10.1080/00397911.2013.813549.
   Web of Science ®Google Scholar
  (g) Kaur, N. Copper Catalysts in the Synthesis of Five-Membered N-Polyheterocycles. Cos. 2018, 15, 940. DOI: 10.2174/1570179415666180815144442.
   Web of Science ®Google Scholar
  (h) Kaur, N. Recent Developments in the Synthesis of Nitrogen Containing Five-Membered Polyheterocycles Using Rhodium Catalysts. Synth. Commun. 2018, 48, 2457. DOI: 10.1080/00397911.2018.1487070.
   Web of Science ®Google Scholar
  (i) Hu, F.; Szostak, M. Recent Developments in the Synthesis and Reactivity of Isoxazoles: Metal Catalysis and Beyond. Adv. Synth. Catal. 2015, 357, 2583. DOI: 10.1002/adsc.201500319.
   Web of Science ®Google Scholar
  (j) Szostak, M.; Shi, S. Nickel-Catalyzed Negishi Cross-Coupling of N-Acylsuccinimides: Stable, Amide-Based, Twist-Controlled Acyl-Transfer Reagents via N–C Activation. Synthesis 2017, 49, 3602. DOI: 10.1055/s-0036-1588845.
   Web of Science ®Google Scholar
  (k) Shi, S.; Meng, G.; Szostak, M. Synthesis of Biaryls Through Nickel-Catalyzed Suzuki-Miyaura Coupling of Amides by Carbon-Nitrogen Bond Cleavage. Angew. Chem. Int. Ed. Engl. 2016, 55, 6959. DOI: 10.1002/anie.201601914.
   PubMed Web of Science ®Google Scholar
• (a) Kaur, N. Microwave-Assisted Synthesis: Fused Five-Membered N -Heterocycles. Syn. Commun. 2015, 45, 789. DOI: 10.1080/00397911.2013.824984.
   Web of Science ®Google Scholar
  (b) Kaur, N. Six-Membered Heterocycles with Three and Four N -Heteroatoms: Microwave-Assisted Synthesis. Synth. Commun. 2015, 45, 151. DOI: 10.1080/00397911.2013.813550.
   Web of Science ®Google Scholar
  (c) Kaur, N. Application of Microwave Irradiation in the Synthesis of Fused Six-Membered Heterocycles with N -Heteroatom. Synth. Commun. 2015, 45, 173.
   Web of Science ®Google Scholar
  (d) Kaur, N. Microwave-Assisted Synthesis of Fused Polycyclic Six-Membered N -Heterocycles. Synth. Commun. 2015, 45, 273. DOI: 10.1080/00397911.2013.816735.
   Web of Science ®Google Scholar
  (e) Kaur, N. Review of Microwave-Assisted Synthesis of Benzo-Fused Six-Membered N,N -Heterocycles. Synth. Commun. 2015, 45, 300. DOI: 10.1080/00397911.2013.816736.
   Web of Science ®Google Scholar
  (f) Kaur, N.; Kishore, D. Synthetic Strategies Applicable in the Synthesis of Privileged Scaffold: 1,4-Benzodiazepine. Synth. Commun. 2014, 44, 1375. DOI: 10.1080/00397911.2013.772202.
   Web of Science ®Google Scholar
  (g) Reddy, M. D.; Blanton, A. N.; Watkins, E. B. Palladium-Catalyzed, N-(2-Aminophenyl)acetamide-Assisted Ortho-Arylation of Substituted Benzamides: Application to the Synthesis of Urolithins B, M6, and M7. J. Org. Chem. 2017, 82, 5080. DOI: 10.1021/acs.joc.7b00256.
   PubMed Web of Science ®Google Scholar
  (h) Reddy, C. R.; Radhika, L.; Kumar, T. P. Chandrasekhar, S. First Acid‐Catalyzed Entry to O‐Alkylated Hydroximides from Benzylic Alcohols. Eur. J. Org. Chem. 2011, 30, 5967. DOI: 10.1002/ejoc.201100797.
   Web of Science ®Google Scholar
• (a) Kaur, N. Environmentally Benign Synthesis of Five-Membered 1,3-N,N-Heterocycles by Microwave Irradiation. Syn. Commun. 2015, 45, 909. DOI: 10.1080/00397911.2013.825808.
   Web of Science ®Google Scholar
  (b) Kaur, N. Advances in Microwave-Assisted Synthesis for Five-Membered N -Heterocycle Synthesis. Synth. Commun. 2015, 45, 432. DOI: 10.1080/00397911.2013.824982.
   Web of Science ®Google Scholar
  (c) Kaur, N. Microwave-Assisted Synthesis of Five-Membered S-Heterocycles. J. Iranian Chem. Soc. 2014, 11, 523. DOI: 10.1007/s13738-013-0325-2.
   Web of Science ®Google Scholar
  (d) Kaur, N. Review on the Synthesis of Six-Membered N,N -Heterocycles by Microwave Irradiation. Synth. Commun. 2015, 45, 1145. DOI: 10.1080/00397911.2013.827208.
   Web of Science ®Google Scholar
  (e) Kaur, N. Greener and Expeditious Synthesis of Fused Six-Membered N,N -Heterocycles Using Microwave Irradiation. Synth. Commun. 2015, 45, 1493.
   Web of Science ®Google Scholar
  (f) Kaur, N. Applications of Microwaves in the Synthesis of Polycyclic Six-Membered N,N -Heterocycles. Synth. Commun. 2015, 45, 1599.
   Web of Science ®Google Scholar
  (g) Kaur, N. Synthesis of Five-Membered N,N,N - and N,N,N,N -Heterocyclic Compounds: Applications of Microwaves. Synth. Commun. 2015, 45, 1711.
   Web of Science ®Google Scholar
  (h) Kaur, N. Palladium Acetate and Phosphine Assisted Synthesis of Five-Membered N -Heterocycles. Synth. Commun. 2019, 49, 483.
   Web of Science ®Google Scholar
• (a) Patil, N. T.; Yamamoto, Y. Coinage Metal-Assisted Synthesis of Heterocycles. Chem. Rev. 2008, 108, 3395. DOI: 10.1021/cr050041j.
   PubMed Web of Science ®Google Scholar
  (b) Reddy, C. R.; Reddy, M. D.; Srikanth, B. Phosphine-Mediated Cascade Reaction of Azides with MBH-Acetates of Acetylenic Aldehydes to Substituted Pyrroles: A Facile Access to N-Fused Pyrrolo-Heterocycles. Org. Biomol. Chem. 2012, 10, 4280. DOI: 10.1039/C2OB25272D.
   PubMed Web of Science ®Google Scholar
  (c) Reddy, C. R.; Krishna, G.; Reddy, M. D. Synthesis of Substituted 3-Furanoates from MBH-Acetates of Acetylenic Aldehydes via Tandem Isomerization–Deacetylation–Cycloisomerization: Access to Elliott’s Alcohol. Org. Biomol. Chem. 2014, 12, 1664. DOI: 10.1039/C3OB42396D.
   PubMed Web of Science ®Google Scholar
  (d) Reddy, M. D.; Uredi, D.; Watkins, E. B. A general method for the metal-free, regioselective, remote C-H halogenation of 8-substituted quinolines. Chem. Sci. 2018, 9, 1782.
   PubMed Web of Science ®Google Scholar
  (e) Sudina, P. R.; Reddy, M. D.; Seema, A. J. Stereocontrolled Total Synthesis of Nonenolide. Nat. Prod. 2018, 81, 1399. DOI: 10.1021/acs.jnatprod.8b00001.
   PubMed Web of Science ®Google Scholar
  (f) Reddy, C. R.; Dilipkumar, U.; Reddy, M. D.; Rao, N. N. Total Synthesis and Revision of the Absolute Configuration of Seimatopolide B. Org. Biomol. Chem. 2013, 11, 3355. DOI: 10.1039/c3ob27518c.
   PubMed Web of Science ®Google Scholar
• (a) Kaur, N. Role of Microwaves in the Synthesis of Fused Five-Membered Heterocycles with Three N -Heteroatoms. Syn. Commun. 2015, 45, 403. DOI: 10.1080/00397911.2013.824981.
   Web of Science ®Google Scholar
  (b) Kaur, N. Recent Impact of Microwave-Assisted Synthesis on Benzo Derivatives of Five-Membered N -Heterocycles. Synth. Commun. 2015, 45, 539.
   Web of Science ®Google Scholar
  (c) Kaur, N.; Kishore, D. Microwave-Assisted Synthesis of Seven- and Higher-Membered N -Heterocycles. Synth. Commun. 2014, 44, 2577. DOI: 10.1080/00397911.2013.783922.
   Web of Science ®Google Scholar
  (d) Kaur, N.; Kishore, D. Microwave-assisted synthesis of six-membered S-heterocycles. Synth. Commun. 2014, 44, 2615.
   Web of Science ®Google Scholar
  (e) Kaur, N.; Kishore, D. Microwave-Assisted Synthesis of Seven- and Higher-Membered O -Heterocycles. Synth. Commun. 2014, 44, 2739. DOI: 10.1080/00397911.2013.796382.
   Web of Science ®Google Scholar
• (a) Alberico, D.; Scott, M. E.; Lautens, M. Aryl–Aryl Bond Formation by Transition-Metal-Catalyzed Direct Arylation. Chem. Rev. 2007, 107, 174. DOI: 10.1021/cr0509760.
   PubMed Web of Science ®Google Scholar
  (b) Kaur, N. Curr. Organocatal 2017, 4, 122.
   Web of Science ®Google Scholar
  (c) Reddy, C. R.; Reddy, M. D. J. Org. Chem. 2014, 79, 106.
   PubMed Web of Science ®Google Scholar
  (d) Raju, G.; Srinivas, R.; Reddy, M. D.; Reddy, C. R.; Nagesh, N. Studies on Non-Covalent Interaction of Coumarin Attached Pyrimidine and 1-Methyl Indole 1,2,3 Triazole Analogues with Intermolecular Telomeric G-Quadruplex DNA Using ESI-MS and Spectroscopy. Nucleosides Nucleotides Nucleic Acids. 2014, 33, 489. DOI: 10.1080/15257770.2014.891742.
   PubMed Web of Science ®Google Scholar
• Dick, A. R.; Sanford, M. S. Transition Metal Catalyzed Oxidative Functionalization of Carbon–Hydrogen Bonds. Tetrahedron 2006, 62, 2439. DOI: 10.1016/j.tet.2005.11.027.
   Web of Science ®Google Scholar
• (a) Kaur, N. Palladium Catalysts: Synthesis of Five-Membered N -Heterocycles Fused with Other Heterocycles. Catal. Rev. 2015, 57, 1.
   Web of Science ®Google Scholar
  (b) Kaur, N.; Kishore, D. Microwave-Assisted Synthesis of Six-Membered O,O -Heterocycles. Synth. Commun. 2014, 44, 3082. DOI: 10.1080/00397911.2013.796384.
   Web of Science ®Google Scholar
  (c) Kaur, N.; Kishore, D. Microwave-Assisted Synthesis of Six-Membered O -Heterocycles. Synth. Commun. 2014, 44, 3047.
   Web of Science ®Google Scholar
  (d) Diez-Gonzalez, S.; Marion, N.; Nolan, S. P. Chem. Rev. 2009, 109, 3612. DOI: 10.1021/cr900074m.
   PubMed Web of Science ®Google Scholar
• Zeni, G.; Larock, R. C. Synthesis of Heterocycles via Palladium-Catalyzed Oxidative Addition . Chem. Rev. 2006, 106, 4644. DOI: 10.1021/cr0683966.
   PubMed Web of Science ®Google Scholar
• Jimenez-Gonzalez, L.; Garcia-Munoz, S.; Alvarez-Corral, M.; Munoz-Dorado, M.; Rodriguez-Garcia, I. Silver-catalyzed asymmetric synthesis of 2,3-dihydrobenzofurans: a new chiral synthesis of pterocarpans. Chem. Eur. J. 2006, 12, 8762.
   PubMed Web of Science ®Google Scholar
• Li, Z.; He, C. Recent Advances in Silver-Catalyzed Nitrene, Carbene, and Silylene-Transfer Reactions. Eur. J. Org. Chem. 2006, 2006, 4313. DOI: 10.1002/ejoc.200500602.
   Web of Science ®Google Scholar
• Miura, T.; Yamauchi, M.; Murakami, M. Nickel-Catalysed Denitrogenative Alkyne Insertion Reactions of N-Sulfonyl-1,2,3-Triazoles. Chem. Commun. 2009, 12, 1470. DOI: 10.1039/b819162j.
   Web of Science ®Google Scholar
• Campana, A. G.; Bazdi, B.; Fuentes, N.; Robles, R.; Cuerva, J. M.; Oltra, J. E.; Porcel, S.; Echavarren, A. M. Divergent Titanium-Mediated Allylations with Modulation by Nickel or Palladium. Angew. Chem. Int. Ed. Engl. 2008, 47, 7515. DOI: 10.1002/anie.200802520.
   PubMed Web of Science ®Google Scholar
• Phapale, V. B.; Bunuel, E.; Garcia-Iglesias, M.; Cardenas, D. Ni-Catalyzed Cascade Formation of C(sp3)-C(sp3) Bonds by Cyclization and Cross-Coupling Reactions of Iodoalkanes with Alkyl Zinc Halides. Angew. Chem. Int. Ed. Engl. 2007, 46, 8790. DOI: 10.1002/anie.200702528.
   PubMed Web of Science ®Google Scholar
• Takimoto, M.; Mori, M. Novel Catalytic CO(2) Incorporation Reaction: Nickel-Catalyzed Regio- and Stereoselective Ring-Closing Carboxylation of Bis-1,3-dienes. J. Am. Chem. Soc. 2002, 124, 10008.
   PubMed Web of Science ®Google Scholar
• Nakamura, I.; Yamamoto, Y. Transition-Metal-Catalyzed Reactions in Heterocyclic Synthesis. Chem. Rev. 2004, 104, 2127. DOI: 10.1021/cr020095i.
   PubMed Web of Science ®Google Scholar
• Caramella, P.; Houk, K. N. Geometries of Nitrilium Betaines. The Clarification of Apparently Anomalous Reactions of 1,3-Dipoles. J. Am. Chem. Soc. 1976, 98, 6397. DOI: 10.1021/ja00436a062.
   Web of Science ®Google Scholar
• Sustmann, R. Orbital Energy Control of Cycloaddition Reactivity. Pure Appl. Chem. 1974, 40, 569. DOI: 10.1351/pac197440040569.
   Web of Science ®Google Scholar
• Hsieh, J.-C.; Ebata, S.; Nakao, Y.; Hiyama, T. Asymmetric Synthesis of Indolines Bearing a Benzylic Quaternary Stereocenter through Intramolecular Arylcyanation of Alkenes. Synlett 2010, 1709. DOI: 10.1055/s-0029-1219964.
   Web of Science ®Google Scholar
• Nakao, Y.; Ebata, S.; Yada, A.; Hiyama, T.; Ikawa, M.; Ogoshi, S. Intramolecular Arylcyanation of Alkenes Catalyzed by nickel/AlMe2Cl. J. Am. Chem. Soc. 2008, 130, 12874. DOI: 10.1021/ja805088r.
   PubMed Web of Science ®Google Scholar
• (a) Oppolzer, W.; Keller, T. H.; Bedoya-Zurita, M.; Stone, C.; Diastereocontrolled Nickel(0)- and Palladium(0) Catalyzed “Metallo-Ene-Type” Cyclizations/Carbonylations. Tetrahedron Lett. 1989, 30, 5883. DOI: 10.1016/S0040-4039(01)93496-3.
   Web of Science ®Google Scholar
  (b) Ojima, C. Chem. Rev. 1996, 96, 642.
   Web of Science ®Google Scholar
  (c) Tzamarioudaki, I.; Li, M.; Donovan, Z. Transition Metal-Catalyzed Carbocyclizations in Organic Synthesis. Chem. Rev. 1996, 96, 635.
   PubMed Web of Science ®Google Scholar
• Lee, E. E.; Rovis, T. Enantioselective Synthesis of Indolizidines Bearing Quaternary Substituted Stereocenters via Rhodium-Catalyzed [2 + 2+2] Cycloaddition of Alkenyl Isocyanates and Terminal Alkynes. Org. Lett. 2008, 10, 1231. DOI: 10.1021/ol800086s.
   PubMed Web of Science ®Google Scholar
• Ashida, S.; Murakami, M. Nickel-Catalyzed [4 + 2+2]-Type Annulation Reaction of Cyclobutanones with Diynes and Enynes. BCSJ. 2008, 81, 885.
   Web of Science ®Google Scholar
• Saito, S.; Maeda, K.; Yamasaki, R.; Kitamura, T.; Nakagawa, M.; Kato, K.; Azumaya, I.; Masu, H. Synthesis of Nine-Membered Carbocycles by the [4 + 3+2] Cycloaddition Reaction of Ethyl Cyclopropylideneacetate and Dienynes. Angew. Chem. Int. Ed. Engl. 2010, 49, 1830. DOI: 10.1002/anie.200907052.
   PubMed Web of Science ®Google Scholar
• Ni, Y.; Montgomery, J. Synthetic Studies and Mechanistic Insight in Nickel-Catalyzed [4 + 2+1] Cycloadditions. J. Am. Chem. Soc. 2006, 128, 2609. DOI: 10.1021/ja057741q.
   PubMed Web of Science ®Google Scholar
• Li, Y.-M.; Li, X.; Peng, F.-Z.; Li, Z.-Q.; Wu, S.-T.; Sun, Z.-W.; Zhang, H.-B.; Shao, Z.-H. Catalytic Asymmetric Construction of Spirocyclopentaneoxindoles by a Combined Ru-Catalyzed Cross-Metathesis/Double Michael Addition Sequence. Org. Lett. 2011, 13, 6200. DOI: 10.1021/ol202624f.
   PubMed Web of Science ®Google Scholar
• Shimizu, K.; Takimoto, M.; Mori, M. Novel Synthesis of Heterocycles Having a Functionalized Carbon Center via nickel-mediated carboxylation: Total Synthesis of Erythrocarine. Org. Lett. 2003, 5, 2323. DOI: 10.1021/ol034670w.
   PubMed Web of Science ®Google Scholar
• Majumdar, K. C.; Muhuri, S.; Islam, R. U.; Chattopadhyay, B. Synthesis of Five- and Six-Membered Heterocyclic Compounds by the Application of the Metathesis Reactions. Heterocycles 2009, 78, 1109. DOI: 10.3987/REV-08-646.
   Web of Science ®Google Scholar
• Kleinman, J. P.; Dubeck, M. The Preparation of Cyclopentadienyl [o-(Phenylazo)Phenyl]Nickel. J. Am. Chem. Soc. 1963, 85, 1544. DOI: 10.1021/ja00893a040.
   Web of Science ®Google Scholar
• Zhang, X.-N.; Li, Y.-X.; Zhang, Z.-H. Nickel Chloride-Catalyzed One-Pot Three-Component Synthesis of Pyrazolophthalazinyl Spirooxindoles. Tetrahedron 2011, 67, 7426. DOI: 10.1016/j.tet.2011.07.002.
   Web of Science ®Google Scholar
• Singh, G. S.; Desta, Z. Y. Isatins as Privileged Molecules in Design and Synthesis of Spiro-Fused Cyclic Frameworks. Chem. Rev. 2012, 112, 6104. DOI: 10.1021/cr300135y.
   PubMed Web of Science ®Google Scholar
• Kotkar, S. P.; Chavan, V. B.; Sudalai, A. Organocatalytic Sequential Alpha-amination-Horner-Wadsworth-Emmons Olefination of Aldehydes: Enantioselective Synthesis of Gamma-Amino-Alpha,Beta-Unsaturated Esters. Org. Lett. 2007, 9, 1001. DOI: 10.1021/ol063012j.
   PubMed Web of Science ®Google Scholar
• Beylin, V.; Boyles, D. C.; Curran, T. T.; Macikenas, D.; Parlett, R. V. IV.; Vrieze, D. The preparation of two, preclinical amino-quinazolinediones as antibacterial agents. Org. Process Res. Dev. 2007, 11, 441.
   Web of Science ®Google Scholar
• Desai, M. C.; Lefkowitz, S. L. Conformationally Restricted Analogs of CP-99,994: Synthesis of a Spirocyclic Amine. Bioorg. Med. Chem. Lett. 1993, 3, 2083. DOI: 10.1016/S0960-894X(01)81021-0.
   Web of Science ®Google Scholar
• Ballini, R.; Petrini, M. Nitroalkanes as key building blocks for the synthesis of heterocyclic derivatives. ARKIVOC. 2009, (ix), 195.
   Google Scholar
• Batcho, A. D.; Leimgruber, W. Org. Synth. 1985, 63, 214.
   Google Scholar
• Denmark, S. E.; Thorarensen, A. The Tandem Cycloaddition Chemistry of Nitroalkenes. A Novel Synthesis of (-)-Hastanecine. J. Org. Chem. 1994, 59, 5672. DOI: 10.1021/jo00098a027.
   Web of Science ®Google Scholar
• Denmark, S. E.; Herbert, B. Synthesis of (-)-7-Epiaustraline and (-)-1-Epicastanospermine. J. Org. Chem. 2000, 65, 2887.
   PubMed Web of Science ®Google Scholar
• Zhao, Z.; Araldi, G. L.; Xiao, Y.; Reddy, A. P.; Liao, Y.; Karra, S.; Brugger, N.; Fischer, D.; Palmer, E. Synthesis and Evaluation of Novel Pyrazolidinone Analogs of PGE2 as EP2 and EP4 Receptors Agonists. Bioorg. Med. Chem. Lett. 2007, 17, 6572. DOI: 10.1016/j.bmcl.2007.09.074.
   PubMed Web of Science ®Google Scholar
• Newkome, G. R.; Moorefield, C. N.; Theriot, K. J. A Convenient Synthesis of Bis-Homotris: 4-Amino-4-[1-(3-Hydroxypropyl)]-1,7-Heptanediol, and 1-Azoniapropellane. J. Org. Chem. 1988, 53, 5552. DOI: 10.1021/jo00258a033.
   Web of Science ®Google Scholar
• Agnieszka, B.; Madeleine, L.; Belen, M.-M. Chem. Eur. J. 2008, 14, 10547.
   PubMed Web of Science ®Google Scholar
• Pathak, R.; Batra, S. Expeditious Synthesis of 5,6,7,8-Tetrahydro-Imidazo[1,2-a]Pyrimidin-2-Ones and 3,4,6,7,8,9-Hexahydro-Pyrimido[1,2-a]Pyrimidin-2-Ones. Tetrahedron 2007, 63, 9448. DOI: 10.1016/j.tet.2007.06.115.
   Web of Science ®Google Scholar
• Nag, S.; Batra, S. Applications of Allylamines for the Syntheses of Aza-Heterocycles. Tetrahedron 2011, 67, 8959. DOI: 10.1016/j.tet.2011.07.087.
   Web of Science ®Google Scholar
• Ezoe, A.; Kimura, M.; Inoue, T.; Mori, M.; Tamaru, Y. Remarkably High 1,5-Diastereoselectivity in a Nickel-Catalyzed Conjugate Addition of Me(2)Zn and Carbonyl Compounds to 1,Omega-Dienynes with Through-Space Coupling. Angew. Chem. Int. Ed. Engl. 2002, 41, 2784. DOI: 10.1002/1521-3773(20020802)41:15<2784::AID-ANIE2784>3.0.CO;2-A.
   PubMed Web of Science ®Google Scholar
• Zuo, G.; Louie, J. Selectivity in Nickel-Catalyzed Rearrangements of Cyclopropylen-ynes. J. Am. Chem. Soc. 2005, 127, 5798. DOI: 10.1021/ja043253r.
   PubMed Web of Science ®Google Scholar
• Dible, B. R.; Sigman, M. S. Steric Effects in the Aerobic Oxidation of Pi-allylnickel(II) Complexes with N-Heterocyclic Carbenes. Inorg. Chem. 2006, 45, 8430. DOI: 10.1021/ic0612451.
   PubMed Web of Science ®Google Scholar
• Jimenez-Nunez, E.; Claverie, C. K.; Nieto-Overhuber, C.; Echavarren, A. M. Angew. Chem. Int. Ed. 2006, 45, 5442.
   Web of Science ®Google Scholar
• Kusama, H.; Suzuki, Y.; Takaya, J.; Iwasawa, N. Intermolecular 1,5-Dipolar Cycloaddition Reaction of Tungsten-Containing Vinylazomethine Ylides Leading to Seven-Membered Heterocycles. Org. Lett. 2006, 8, 895. DOI: 10.1021/ol0529795.
   PubMed Web of Science ®Google Scholar
• Joensuu, P. M.; Murray, G. J.; Fordyce, E. A. F.; Luebbers, T.; Lam, H. W. Diastereoselective Nickel-Catalyzed Reductive Aldol Cyclizations Using Diethylzinc as the Stoichiometric Reductant: Scope and Mechanistic Insight. J. Am. Chem. Soc. 2008, 130, 7328. DOI: 10.1021/ja0775624.
   PubMed Web of Science ®Google Scholar
• (a) Zhao, C.; Wang, H.; Zhao, G. Synthesis 2009, 11, 1785.
   Google Scholar
  (b)Yu, Z.-X.; Wang, Y.; Wang, Y. Transition-Metal-Catalyzed Cycloadditions for the Synthesis of Eight-Membered Carbocycles. Chem. Asian J. 2010, 5, 1072. DOI: 10.1002/asia.200900712.
   PubMed Web of Science ®Google Scholar
• Wender, P. A.; Christy, J. P. Nickel(0)-Catalyzed [2 + 2 + 2 + 2] Cycloadditions of Terminal Diynes for the Synthesis of Substituted Cyclooctatetraenes . J. Am. Chem. Soc. 2007, 129, 13402. DOI: 10.1021/ja0763044.
   PubMed Web of Science ®Google Scholar
• (a) Wender, P. A.; Christy, J. P.; Lesser, A. B.; Gieseler, M. T. Angew. Chem. Int. Ed. 2009, 121, 7823;
   Google Scholar
  (b) Wender, P. A.; Christy, J. P.; Lesser, A. B.; Gieseler, M. T. The Synthesis of Highly Substituted Cyclooctatetraene Scaffolds by Metal‐Catalyzed [2 + 2+2 + 2] Cycloadditions: Studies on Regioselectivity, Dynamic Properties, and Metal Chelation. Angew. Chem. Int. Ed. 2009, 48, 7687. DOI: 10.1002/anie.200903859.
   PubMed Web of Science ®Google Scholar
• Goswami, A.; Ito, T.; Saino, N.; Kase, K.; Matsuno, C.; Okamoto, S. Selective Dimerization of 1,6-Diynes Catalyzed by Ionic Liquid-Supported Nickel Complexes in an Ionic Liquid/Toluene Biphasic System. Chem. Commun. 2009, 4, 439. DOI: 10.1039/B816850D.
   Web of Science ®Google Scholar
• Murakami, M.; Ashida, S.; Matsuda, T. Eight-Membered Ring Construction by [4 + 2 + 2] Annulation Involving Beta-Carbon Elimination. J. Am. Chem. Soc. 2006, 128, 2166. DOI: 10.1021/ja0552895.
   PubMed Web of Science ®Google Scholar
• Oppolzer, W. Intramolecular, Stoichiometric (Li, Mg, Zn) and Catalytic (Ni, Pd, Pt) Metallo-Ene Reactions in Organic Synthesis [New Synthetic Methods (75)]. Angew Chem. Int. Ed. Engl. 1989, 28, 38. DOI: 10.1002/anie.198900381.
   Web of Science ®Google Scholar
• Oppolzer, W. Regio- and Stereocontrolled Catalytic Palladium- and Nickel 'ene-Type' Cyclizations. Pure Appl. Chem. 1990, 62, 1941. DOI: 10.1351/pac199062101941.
   Web of Science ®Google Scholar
• Turek, P.; Kotora, M.; Hocek, M.; Cı́sařová, I. [2 + 2+2]-Co-Cyclotrimerization 6-Alkynylpurines with Diynes: A Method for Preparation of 6-Arylpurines. Tetrahedron Lett. 2003, 44, 785.
   Web of Science ®Google Scholar
• Turek, P.; Kotora, M.; Tislerova, I.; Hocek, M.; Votruba, I.; Cisarova, I. Cocyclotrimerization of 6-Alkynylpurines with Alpha,Omega-Diynes as a Novel Approach to Biologically Active 6-Arylpurines. J. Org. Chem. 2004, 69, 9224. DOI: 10.1021/jo0486342.
   PubMed Web of Science ®Google Scholar
• Kotha, S.; Brahmachary, E.; Lahiri, K. Transition Metal Catalyzed [2 + 2+2] Cycloaddition and Application in Organic Synthesis. Eur. J. Org. Chem. 2005, 2005, 4741. DOI: 10.1002/ejoc.200500411.
   Web of Science ®Google Scholar
• Wender, P. A.; Ihle, N. C. Nickel-Catalyzed Intramolecular [4 + 4]-Cycloadditions: A New Method for the Synthesis of Polycycles Containing Eight-Membered Rings. J. Am. Chem. Soc. 1986, 108, 4678. DOI: 10.1021/ja00275a085.
   Web of Science ®Google Scholar
• Wender, P. A.; Snapper, M. L. Intramolecular Nickel Catalyzed Cycloadditions of Bis-Dienes: 3 Approaches to the Taxane Skeleton. Tetrahedron Lett. 1987, 28, 2221. DOI: 10.1016/S0040-4039(00)96085-4.
   Web of Science ®Google Scholar
• Wender, P. A.; Jenkins, T. E. Nickel-Catalyzed Intramolecular [4 + 2] Dienyne Cycloadditions: An Efficient New Method for the Synthesis of Polycycles Containing Cyclohexa-1,4-Dienes. J. Am. Chem. Soc. 1989, 111, 6432. DOI: 10.1021/ja00198a071.
   Web of Science ®Google Scholar
• Shanmugasundaram, M.; Wu, M.-S.; Jeganmohan, M.; Huang, C.-W.; Cheng, C.-H. Highly Regio- and Chemoselective [2 + 2 + 2] Cycloaddition of Electron-Deficient Diynes with Allenes Catalyzed by Nickel Complexes: A Novel Entry to Polysubstituted Benzene Derivatives. J. Org. Chem. 2002, 67, 7724.
   PubMed Web of Science ®Google Scholar
• Wattenbach, C.; Maurer, M.; Frauenrath, H. A Novel Synthesis of 4-Methyl-1,3-Dioxolane-4-Carbaldehydes by Epoxidation of 5-Methyl-4H-1,3-Dioxins and Acid-Catalyzed Rearrangement. Synlett 1999, 3, 303. DOI: 10.1055/s-1999-2601.
   Google Scholar
• Frimer, A. A. Synthesis of α-Hydroxyacetals. Synthesis 1977, 8, 578. DOI: 10.1055/s-1977-24486.
   Google Scholar
• Hoppe, D.; Lüßmann, J.; Jones, P. G.; Schmidt, D.; Sheldrick, G. M. Highly Diastereoselective Synthesis of 1,2-Epoxy-4-Hydroxyalkyl Carbamates. Masked and Activated α,γ-Dihydroxy-Alkanals and -Alkanones. Tetrahedron Lett. 1986, 27, 3591. DOI: 10.1016/S0040-4039(00)84857-1.
   Web of Science ®Google Scholar
• Matsumoto, K.; Ozaki, Y.; Suzuki, M.; Miyoshi, M. A Stereoselective Synthesis of threo-Threonine Reaction of Isocyanoacetate with Acetaldehyde. Agric. Biol. Chem. 1976, 40, 2045. DOI: 10.1080/00021369.1976.10862337.
   Web of Science ®Google Scholar
• Gulevich, A. V.; Zhdanko, A. G.; Orru, R. V. A.; Nenajdenko, V. G. Isocyanoacetate Derivatives: Synthesis, Reactivity, and Application. Chem. Rev. 2010, 110, 5235. DOI: 10.1021/cr900411f.
   PubMed Web of Science ®Google Scholar
• Wattenbach, C.; Palme-Konig, R.; Flock, S.; Muller, U.; Frauenrath, H. Z. K. NCS. 2001, 216, 399.
   Web of Science ®Google Scholar
• Wattenbach, C.; Palme-Konig, R.; Flock, S.; Muller, U.; Frauenrath, H. Z. K. NCS. 2001, 216, 401.
   Web of Science ®Google Scholar
• Munegumi, T.; Azumaya, I.; Kato, T.; Masu, H.; Saito, S. [3 + 2] Cross-Coupling Reactions of Aziridines with Isocyanates Catalyzed by Nickel(II) Iodide. Org. Lett. 2006, 8, 379.
   PubMed Web of Science ®Google Scholar
• Zhang, M.; Buchwald, S. L. A Nickel(0)-Catalyzed Process for the Transformation of Enynes to Bicyclic Cyclopentenones. J. Org. Chem. 1996, 61, 4498.
   PubMed Web of Science ®Google Scholar
• Wender, P. A.; Smith, T. E. Transition Metal-Catalyzed Intramolecular [4 + 2] Cycloadditions: Initial Studies on Stereochemistry and on Steroid and Vitamin D Analog Syntheses. J. Org. Chem. 1995, 60, 2962. DOI: 10.1021/jo00115a006.
   Web of Science ®Google Scholar
• Tamao, K.; Kobayashi, K.; Ito, Y. Nickel(0)-Promoted Cyclization of Enynes with Isocyanides: A New Route to Polycyclic Cyclopentenone Skeletons. J. Am. Chem. Soc. 1988, 110, 1286. DOI: 10.1021/ja00212a045.
   Web of Science ®Google Scholar
• Cravino, A.; Zerza, G.; Neugebauer, H.; Maggini, M.; Bucella, S.; Menna, E.; Svensson, M.; Andersson, M. R.; Brabec, C. J.; Sariciftci, N. S. Electrochemical and Photophysical Properties of a Novel Polythiophene with Pendant Fulleropyrrolidine Moieties: Toward “Double Cable” Polymers for Optoelectronic Devices. J. Phys. Chem. B. 2002, 106, 70. DOI: 10.1021/jp013077y.
   Web of Science ®Google Scholar
• Goto, H.; Okamoto, Y.; Yashima, E. Solvent-Induced Chiroptical Changes in Supramolecular Assemblies of an Optically Active, Regioregular Polythiophene. Macromolecules 2002, 35, 4590. DOI: 10.1021/ma012083p.
   Web of Science ®Google Scholar
• Tovar, J. D.; Swager, T. M. Poly(Naphthodithiophene)s: Robust, Conductive Electrochromics via Tandem Cyclization-Polymerizations. Adv. Mater. 2001, 13, 1775. DOI: 10.1002/1521-4095(200112)13:23<1775::AID-ADMA1775>3.0.CO;2-N.
   Web of Science ®Google Scholar
• Takagi, K. A Facile Synthesis of Sulfides Using S -Aryl-Isothiuronium Intermediates. Chem. Lett. 1986, 15, 1379. DOI: 10.1246/cl.1986.1379.
   Web of Science ®Google Scholar
• Kondo, T.; Mitsudo, T.-A. Metal-Catalyzed Carbon-Sulfur Bond Formation. Chem. Rev. 2000, 100, 3205.
   PubMed Web of Science ®Google Scholar