Advanced search
Publication Cover
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 33, 2003 - Issue 13
Submit an article Journal homepage
430
Views
34
CrossRef citations to date
0
Altmetric
Original Articles

Microwave Assisted Pictet–Spengler and Bischler–Napieralski Reactions

Bikash Pal Department of Medicinal Chemistry, Indian Institute of Chemical Biology, Calcutta, West Bengal, India
,
Parasuraman Jaisankar Department of Medicinal Chemistry, Indian Institute of Chemical Biology, Calcutta, West Bengal, India
&
Venkatachalam S. Giri Department of Medicinal Chemistry, Indian Institute of Chemical Biology, Calcutta, West Bengal, IndiaCorrespondence[email protected]
Pages 2339-2348 | Received 14 Oct 2002, Published online: 17 Aug 2006

Citations (34)

Keep up to date with the latest research on this topic with citation updates for this article.

Subscribe to citation updates

Read on this site (2)

Fei Liu & Qi‐Dong You. (2007) Microwave‐Assisted One‐Pot Preparation of Tetrahydro‐β‐carboline Hydrochlorides under Solvent‐Free Conditions. Synthetic Communications 37:22, pages 3933-3938.
Read now
Prasun K. Pradhan, Parasuraman Jaisankar, Bikash Pal, Sumit Dey & Venkatachalam S. Giri. (2004) Selective Reduction of Aldehydes to Alcohols Using Alumina with a Catalytic Amount of Base Under Microwave Irradiation. Synthetic Communications 34:15, pages 2863-2872.
Read now

Articles from other publishers (32)

Avneesh AwasthyOm Prakash Agrawal. (2022) Synthesis and Antimicrobial and Anticancer Activity of β-Carboline Analogues. Research Journal of Pharmacy and Technology, pages 3969-3974.
Crossref
Jay Prakash Soni, Manda Sathish, Fabiane M. Nachtigall, Leonardo S. Santos & Nagula Shankaraiah. (2022) Brown Seaweed‐Derived Alginic Acid: An Efficient and Reusable Catalyst for Pictet‐Spengler Reaction to Access Tetrahydro‐ β ‐Carboline and Tetrahydroisoquinoline Frameworks . Asian Journal of Organic Chemistry 11:5.
Crossref
Mengwei Li, Yuan Yuan & Yulan Chen. (2021) Bischler‐Napieralski Cyclization: A Versatile Reaction towards Functional Aza‐PAHs and Their Conjugated Polymers † . Chinese Journal of Chemistry 39:11, pages 3101-3115.
Crossref
Surya K. De. 2021. Applied Organic Chemistry. Applied Organic Chemistry 469 506 .
Somnath S. Gholap & Vinod R. Kadu. (2021) Natural surfactants assisted an efficient synthesis of tetrahydro-β-carbolines. Results in Chemistry 3, pages 100183.
Crossref
Pradipta Maity, Debasis Adhikari & Amit Kumar Jana. (2019) An overview on synthetic entries to tetrahydro-β-carbolines. Tetrahedron 75:8, pages 965-1028.
Crossref
Takumi Abe & Koji Yamada. (2017) Concise Syntheses of Hyrtioreticulins C and D via a C-4 Pictet–Spengler Reaction: Revised Signs of Specific Rotations. Journal of Natural Products 80:2, pages 241-245.
Crossref
THOKCHOM PRASANTA SINGH & OKRAM MUKHERJEE SINGH. (2016) One pot synthesis of 1-substituted tetrahydro-β-carbolines by Bischler–Napieralski cyclization. Journal of Chemical Sciences 128:4, pages 565-572.
Crossref
Scott Handy & Matthew Wright. (2014) An acid-free Pictet–Spengler reaction using deep eutectic solvents (DES). Tetrahedron Letters 55:23, pages 3440-3442.
Crossref
Scott Eagon & Marc O. Anderson. (2014) Microwave‐Assisted Synthesis of Tetrahydro‐β‐carbolines and β‐Carbolines. European Journal of Organic Chemistry 2014:8, pages 1653-1665.
Crossref
Ashish Sharma, Mrityunjay Singh, Nitya Nand Rai & Devesh Sawant. (2013) Mild and efficient cyanuric chloride catalyzed Pictet–Spengler reaction. Beilstein Journal of Organic Chemistry 9, pages 1235-1242.
Crossref
Armand Gellis, Aurélien Dumètre, Gilles Lanzada, Sébastien Hutter, Evelyne Ollivier, Patrice Vanelle & Nadine Azas. (2012) Preparation and antiprotozoal evaluation of promising β-carboline alkaloids. Biomedicine & Pharmacotherapy 66:5, pages 339-347.
Crossref
Rami A. Al-Horani & Umesh R. Desai. (2012) Electronically rich N-substituted tetrahydroisoquinoline 3-carboxylic acid esters: concise synthesis and conformational studies. Tetrahedron 68:8, pages 2027-2040.
Crossref
Haifeng Gan, Yunyu Lu, Yue Huang, Lijun Ni, Jinyi Xu, Hequan Yao & Xiaoming Wu. (2011) Oxidation of 1-benzyldihydroisoquinolines or 1-benzyltetrahydroisoquinolines with dioxygen to 1-benzoylisoquinolines. Tetrahedron Letters 52:12, pages 1320-1324.
Crossref
Shengkun Li, Bing YangQianliang ZhangJiwen Zhang, Junru Wang & Wenjun Wu. (2010) Synthesis and Bioactivity of β-Carboline Derivatives. Natural Product Communications 5:10, pages 1934578X1000501.
Crossref
Zerong Wang. 2010. Comprehensive Organic Name Reactions and Reagents. Comprehensive Organic Name Reactions and Reagents 9 12 .
Emelia Awuah & Alfredo Capretta. (2010) Strategies and Synthetic Methods Directed Toward the Preparation of Libraries of Substituted Isoquinolines. The Journal of Organic Chemistry 75:16, pages 5627-5634.
Crossref
YuFeng Wang, ZhanBo Song, ChunXia Chen & JinSong Peng. (2010) Pictet-Spengler condensation reactions catalyzed by a recyclable H+-montmorillonite as a heterogeneous Brønsted acid. Science China Chemistry 53:3, pages 562-568.
Crossref
Richard J. Sundberg. 2010. Heterocyclic Scaffolds II:. Heterocyclic Scaffolds II: 47 115 .
J. Phillip Kennedy, Micah L. Breininger & Craig W. Lindsley. (2009) Total synthesis of Eudistomins Y1–Y6. Tetrahedron Letters 50:50, pages 7067-7069.
Crossref
Nuno R. Candeias, Luís C. Branco, Pedro M. P. Gois, Carlos A. M. Afonso & Alexandre F. Trindade. (2009) More Sustainable Approaches for the Synthesis of N-Based Heterocycles. Chemical Reviews 109:6, pages 2703-2802.
Crossref
Chih-Shone Lee, Cheng-Kuo Liu, Yen-Yao Cheng & Che-Ming Teng. (2009) A New and Facile Synthesis of Rutaecarpine Alkaloids. HETEROCYCLES 78:4, pages 1047.
Crossref
Rosaria Gitto, Rita Ficarra, Rosanna Stancanelli, Marta Guardo, Laura De Luca, Maria Letizia Barreca, Benedetta Pagano, Archimede Rotondo, Giuseppe Bruno, Emilio Russo, Giovanbattista De Sarro & Alba Chimirri. (2007) Synthesis, resolution, stereochemistry, and molecular modeling of (R)- and (S)-2-acetyl-1-(4′-chlorophenyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline AMPAR antagonists. Bioorganic & Medicinal Chemistry 15:16, pages 5417-5423.
Crossref
Adrienn Hegedüs, Zoltán Hell & Attila Potor. (2006) A new, environmentally-friendly method for the Bischler–Napieralski cyclization using zeolite catalyst. Catalysis Communications 7:12, pages 1022-1024.
Crossref
Nicholas E. Leadbeater & Hanna M. Torenius. 2006. Microwaves in Organic Synthesis. Microwaves in Organic Synthesis 327 361 .
Antonino Corsaro, Ugo Chiacchio, Venerando Pistará & Giovanni Romeo. 2006. Microwaves in Organic Synthesis. Microwaves in Organic Synthesis 579 614 .
Kazuhiro Kobayashi, Taiyo Shiokawa, Hiroki Omote, Kenichi Hashimoto, Osamu Morikawa & Hisatoshi Konishi. (2006) New Synthesis of Isoquinoline and 3,4-Dihydroisoquinoline Derivatives. Bulletin of the Chemical Society of Japan 79:7, pages 1126-1132.
Crossref
Brian E. Love. 2006. Heterocyclic Antitumor Antibiotics. Heterocyclic Antitumor Antibiotics 93 128 .
Fu-Ming Kuo, Ming-Chung Tseng, Ya-Hew Yen & Yen-Ho Chu. (2004) Microwave accelerated Pictet–Spengler reactions of tryptophan with ketones directed toward the preparation of 1,1-disubstituted indole alkaloids. Tetrahedron 60:52, pages 12075-12084.
Crossref
Ya-Hew Yen & Yen-Ho Chu. (2004) Synthesis of tetrahydro-β-carbolinediketopiperazines in [bdmim][PF6] ionic liquid accelerated by controlled microwave heating. Tetrahedron Letters 45:44, pages 8137-8140.
Crossref
Kazuhiro Kobayashi, Taiyo Shiokawa, Osamu Morikawa & Hisatoshi Konishi. (2004) New Synthesis of Isoquinoline Derivatives by Reactions of 2-(2-Methoxyethenyl)benzonitriles with Organolithiums and Lithium Dialkylamides. Chemistry Letters 33:3, pages 236-237.
Crossref
Bikash Pal, Parasuraman Jaisankar & Venkatachalam S. Giri. (2003) Microwave Assisted Pictet—Spengler and Bischler—Napieralski Reactions.. ChemInform 34:44.
Crossref

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.