Citations (56)
Keep up to date with the latest research on this topic with citation updates for this article.
Articles from other publishers (56)
Miguel Adrián Márquez-Cadena, Wei Zhang & Rongbiao Tong. (2021) Synthetic Studies toward the Berkeleyacetal Core Architecture. Organic Letters 23:23, pages 9227-9231.
Crossref
Crossref
Qingzhao Xing, Zhe Hao, Jing Hou, Gaoqiang Li, Ziwei Gao, Jing Gou, Chaoqun Li & Binxun Yu. (2021)
Manganese-Catalyzed Achmatowicz Rearrangement Using Green Oxidant H
2
O
2
. The Journal of Organic Chemistry 86:14, pages 9563-9586.
Crossref
Crossref
Guodong Zhao, Lixin Liang, Eryu Wang & Rongbiao Tong. (2021) Fenton Chemistry for Achmatowicz Rearrangement. ACS Catalysis 11:6, pages 3740-3748.
Crossref
Crossref
Tohru Oishi, Yuta Watanabe, Kohei Torikai & Yoko Yasuno. (2021) Synthetic Study of the C’D’E’ Ring System of Maitotoxin via Furan Based Strategy. HETEROCYCLES 102:12, pages 2313.
Crossref
Crossref
Guodong Zhao & Rongbiao Tong. (2019) Silica gel enables Achmatowicz rearrangement with KBr/oxone under “anhydrous” condition for one-pot functionalization. Tetrahedron 75:12, pages 1669-1675.
Crossref
Crossref
Guodong Zhao & Rongbiao Tong. (2019) A solvent-free catalytic protocol for the Achmatowicz rearrangement. Green Chemistry 21:1, pages 64-68.
Crossref
Crossref
Wang-Ze Song, Yu-Bin Zheng, Ming Li, Nan Zheng, Karim Ullah, Jun-Hao Li & Kun Dong. (2018) Vanadium-Catalyzed Achmatowicz and Aza-Achmatowicz Rearrangement Reactions. HETEROCYCLES 96:10, pages 1779.
Crossref
Crossref
Xin Liu, Ya-Jian Hu, Jian-Hong Fan, Jing Zhao, Shaoping Li & Chuang-Chuang Li. (2018)
Recent synthetic studies towards natural products
via
[5 + 2] cycloaddition reactions
. Organic Chemistry Frontiers 5:7, pages 1217-1228.
Crossref
Crossref
Silvia Roscales & Joaquín Plumet. (2019) Ring Rearrangement Metathesis in 7-Oxabicyclo[2.2.1]heptene (7-Oxanorbornene) Derivatives. Some Applications in Natural Product Chemistry. Natural Product Communications 12:5, pages 1934578X1701200.
Crossref
Crossref
Matthew B. Plutschack, Peter H. Seeberger & Kerry Gilmore. (2016) Visible-Light-Mediated Achmatowicz Rearrangement. Organic Letters 19:1, pages 30-33.
Crossref
Crossref
Zhilong Li & Rongbiao Tong. (2016) Catalytic Environmentally Friendly Protocol for Achmatowicz Rearrangement. The Journal of Organic Chemistry 81:11, pages 4847-4855.
Crossref
Crossref
Arun K. Ghosh & Margherita Brindisi. (2016) Achmatowicz reaction and its application in the syntheses of bioactive molecules. RSC Advances 6:112, pages 111564-111598.
Crossref
Crossref
Andrea Gelmini, Stefania Albonetti, Fabrizio Cavani, Cristiana Cesari, Alice Lolli, Valerio Zanotti & Rita Mazzoni. (2016) Oxidant free one-pot transformation of bio-based 2,5-bis-hydroxymethylfuran into α-6-hydroxy-6-methyl-4-enyl-2H-pyran-3-one in water. Applied Catalysis B: Environmental 180, pages 38-43.
Crossref
Crossref
Pedro Merino. 2004. Organic Reactions. Organic Reactions
1
256
.
Yining Ji, Tamas Benkovics, Gregory L. Beutner, Chris Sfouggatakis, Martin D. Eastgate & Donna G. Blackmond. (2015) Mechanistic Insights into the Vanadium-Catalyzed Achmatowicz Rearrangement of Furfurol. The Journal of Organic Chemistry 80:3, pages 1696-1702.
Crossref
Crossref
Na Liu, Wangze Song, Casi M. Schienebeck, Min Zhang & Weiping Tang. (2014) Synthesis of naturally occurring tropones and tropolones. Tetrahedron 70:49, pages 9281-9305.
Crossref
Crossref
Daniel Thiel, Diana Doknić & Jan Deska. (2014) Enzymatic aerobic ring rearrangement of optically active furylcarbinols. Nature Communications 5:1.
Crossref
Crossref
Matthew J. Palframan & Gerald Pattenden. (2014) The versatility of furfuryl alcohols and furanoxonium ions in synthesis. Chemical Communications 50:55, pages 7223.
Crossref
Crossref
Tamsyn Montagnon, Dimitris Kalaitzakis, Myron Triantafyllakis, Manolis Stratakis & Georgios Vassilikogiannakis. (2014) Furans and singlet oxygen ? why there is more to come from this powerful partnership. Chem. Commun. 50:98, pages 15480-15498.
Crossref
Crossref
Min Zhang, Na Liu & Weiping Tang. (2013) Stereoselective Total Synthesis of Hainanolidol and Harringtonolide via Oxidopyrylium-Based [5 + 2] Cycloaddition. Journal of the American Chemical Society 135:33, pages 12434-12438.
Crossref
Crossref
Chimène Asta, Dietmar Schmidt, Jürgen Conrad, Bernhard Förster-Fromme, Till Tolasch & Uwe Beifuss. (2013) The first enzymatic Achmatowicz reaction: selective laccase-catalyzed synthesis of 6-hydroxy-(2H)-pyran-3(6H)-ones and (2H)-pyran-2,5(6H)-diones. RSC Advances 3:42, pages 19259.
Crossref
Crossref
Dimitris Noutsias, Ioanna Alexopoulou, Tamsyn Montagnon & Georgios Vassilikogiannakis. (2012) Using water, light, air and spirulina to access a wide variety of polyoxygenated compounds. Green Chemistry 14:3, pages 601.
Crossref
Crossref
Fiona Serra, Philippe Coutrot, Mélanie Estève‐Quelquejeu, Patrick Herson, Tomasz K. Olszewski & Claude Grison. (2011) Diastereoselective Synthesis of Lincosamine Precursors. European Journal of Organic Chemistry 2011:10, pages 1841-1847.
Crossref
Crossref
Dimitris Noutsias, Antonia Kouridaki & Georgios Vassilikogiannakis. (2011)
Scope and Limitations of the Photooxidations of 2-(α-Hydroxyalkyl)furans: Synthesis of 2-Hydroxy-
exo
-brevicomin
. Organic Letters 13:5, pages 1166-1169.
Crossref
Crossref
Arun K. Ghosh & Jianfeng Li. (2010) A Stereoselective Synthesis of (+)-Herboxidiene/GEX1A. Organic Letters 13:1, pages 66-69.
Crossref
Crossref
Tamsyn Montagnon, Dimitris Noutsias, Ioanna Alexopoulou, Maria Tofi & Georgios Vassilikogiannakis. (2011) Green oxidations of furans—initiated by molecular oxygen—that give key natural product motifs. Organic & Biomolecular Chemistry 9:7, pages 2031.
Crossref
Crossref
Zerong Wang. 2010. Comprehensive Organic Name Reactions and Reagents. Comprehensive Organic Name Reactions and Reagents
2580
2585
.
Zerong Wang. 2010. Comprehensive Organic Name Reactions and Reagents. Comprehensive Organic Name Reactions and Reagents
1046
1050
.
Takashi Nagano, Jiři Pospíšil, Guillaume Chollet, Saskia Schulthoff, Volker Hickmann, Emilie Moulin, Jennifer Herrmann, Rolf Müller & Alois Fürstner. (2009) Total Synthesis and Biological Evaluation of the Cytotoxic Resin Glycosides Ipomoeassin A-F and Analogues. Chemistry - A European Journal 15:38, pages 9697-9706.
Crossref
Crossref
Katrina L. Jackson, James A. Henderson, Hajime Motoyoshi & Andrew J. Phillips. (2009) A Total Synthesis of Norhalichondrin B. Angewandte Chemie International Edition 48:13, pages 2346-2350.
Crossref
Crossref
Katrina L. Jackson, James A. Henderson, Hajime Motoyoshi & Andrew J. Phillips. (2009) A Total Synthesis of Norhalichondrin B. Angewandte Chemie 121:13, pages 2382-2386.
Crossref
Crossref
Alois Fürstner & Takashi Nagano. (2007) Total Syntheses of Ipomoeassin B and E. Journal of the American Chemical Society 129:7, pages 1906-1907.
Crossref
Crossref
Paul A. Wender, F. Christopher Bi, Nicole Buschmann, Francis Gosselin, Cindy Kan, Jung-Min Kee & Hirofumi Ohmura. (2006) Studies on Oxidopyrylium [5 + 2] Cycloadditions: Toward a General Synthetic Route to the C12-Hydroxy Daphnetoxins. Organic Letters 8:23, pages 5373-5376.
Crossref
Crossref
Sylvain Celanire, Frederic Marlin, Jack E. Baldwin & Robert M. Adlington. (2005) Base-assisted intramolecular 6-acetoxypyranone-acetylene [5+2] cycloaddition. Synthesis and reactivity of novel oxa-tricyclo[5.3.1.01,5]undecenones. Tetrahedron 61:12, pages 3025-3032.
Crossref
Crossref
U. Murali Krishna, Kodand D. Deodhar & Girish K. Trivedi. (2004) Asymmetric oxidopyrylium-alkene [5+2] cycloaddition: a divergent approach for the synthesis of enantiopure oxabicyclo[5.4.0]undecanes. Tetrahedron 60:22, pages 4829-4836.
Crossref
Crossref
Michael E. Jung & Joseph Pontillo. (2002) Synthetic Approach to Analogues of the Original Structure of Sclerophytin A. The Journal of Organic Chemistry 67:19, pages 6848-6851.
Crossref
Crossref
Ken-ichi Takao, Gohshi Watanabe, Hiroyuki Yasui & Kin-ichi Tadano. (2002) Total Synthesis of (±)-Mycoepoxydiene, a Novel Fungal Metabolite Having an Oxygen-Bridged Cyclooctadiene Skeleton. Organic Letters 4:17, pages 2941-2943.
Crossref
Crossref
Antonio Massa, Francesca R Siniscalchi, Valeria Bugatti, Alessandra Lattanzi & Arrigo Scettri. (2002) New procedures for the enantioselective oxidation of sulfides under stoichiometric and catalytic conditions. Tetrahedron: Asymmetry 13:12, pages 1277-1283.
Crossref
Crossref
Antonio Massa, Laura Palombi & Arrigo Scettri. (2001) A convenient approach to renewable hydroperoxides. Tetrahedron Letters 42:27, pages 4577-4579.
Crossref
Crossref
Philip Magnus & Lan Shen. (1999) Stereoselective synthesis of the “cyathin” diterpene skeleton via an intramolecular pyrylium ylide-alkene cyclization. Tetrahedron 55:12, pages 3553-3560.
Crossref
Crossref
William E. Bauta, John Booth, Mary E. Bos, Mark DeLuca, Louis Diorazio, Timothy J. Donohoe, Christopher Frost, Nicholas Magnus, Philip Magnus, José Mendoza, Philip Pye, James G. Tarrant, Stephen Thom & Feroze Ujjainwalla. (1996) Taxane diterpenes 1. Control of relative and absolute stereochemistry in intramolecular pyrylium ylide-alkene cyclizations for the synthesis of taxol precursors. Tetrahedron 52:45, pages 14081-14102.
Crossref
Crossref
Philip Magnus, Louis Diorazio, Timothy J. Donohoe, Melvyn Giles, Philip Pye, James Tarrant & Stephen Thom. (1996) Taxane diterpenes 3: Formation of the eight-membered B-ring by semi-pinacol rearrangement. Tetrahedron 52:45, pages 14147-14176.
Crossref
Crossref
Waldemar Adam & Rosemarie M. Schuhmann. (2006) Selective Oxyfunctionalization of (Tricarbonylcyclohexadiene)iron‐Substituted Furans with Singlet Oxygen and Dimethyldioxirane. Liebigs Annalen 1996:4, pages 635-640.
Crossref
Crossref
. 1996. Comprehensive Heterocyclic Chemistry II. Comprehensive Heterocyclic Chemistry II
969
1102
.
Harry Heaney & Jeong Soo Ahn. 1996. Comprehensive Heterocyclic Chemistry II. Comprehensive Heterocyclic Chemistry II
297
350
.
Jerzy Raczko & Janusz Jurczak. 1995. Stereoselective Synthesis (Part J). Stereoselective Synthesis (Part J)
639
685
.
. 1995. Comprehensive Organic Functional Group Transformations. Comprehensive Organic Functional Group Transformations
727
856
.
Warren J. Ebenezer & Paul Wight. 1995. Comprehensive Organic Functional Group Transformations. Comprehensive Organic Functional Group Transformations
205
276
.
Gu Jian-Xin, Li Zu-Yi & Lin Guo-Qiang. (1993) Reductive biotransformation of carbonyl compounds—application of fungus, Geotrichum sp. G38 in organic synthesis. Tetrahedron 49:26, pages 5805-5816.
Crossref
Crossref
Ian Paterson, M.Anne Lister & Glen R. Ryan. (1991) Asymmetric aldol reactions using chiral boron reagents: Application to the synthesis of tirandamycin A. Tetrahedron Letters 32:14, pages 1749-1752.
Crossref
Crossref
Stephen F. Martin, Charles Gluchowski, Carlton L. Campbell & Robert C. Chapman. (1988) A concise route to a key intermediate in the total syntheses of (+)-tirandamycic acid and (-)-tirandamycin a †. Tetrahedron 44:11, pages 3171-3180.
Crossref
Crossref
Stephen F. Martin. 1988. Natural Products Chemistry III. Natural Products Chemistry III
135
153
.
Louis S. Hegedus. (1985) Transition metals in organic synthesis. Journal of Organometallic Chemistry 283:1-3, pages 1-219.
Crossref
Crossref
Stephen F. Martin & Denise E. Guinn. (1984) Furans as intermediates for the synthesis of oxygenated natural products. Asymmetric synthesis of Prelog-Djerassi lactone.. Tetrahedron Letters 25:49, pages 5607-5610.
Crossref
Crossref
Yuichi Kobayashi, Harutaka Katsuno & Fumie Sato. (1983)
PERACID-INDUCED OXIDATION OF 2,5-DISUBSTITUTED FURANS TO
CIS
-1,2-DIACYLETHYLENES
. Chemistry Letters 12:11, pages 1771-1774.
Crossref
Crossref
T. H. HO & S. G. SAPP. (2016) ChemInform Abstract: SHARPLESS EPOXIDATION OF 2‐FURANCARBINOLS. MASS SPECTRA OF 6‐HYDROXY‐3(2H)‐PYRANONES. Chemischer Informationsdienst 14:37.
Crossref
Crossref