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Angewandte Chemie - International Edition

Volumn 39, Issue 24, 2000, Pages 4502-4505

Stereoselective total synthesis of zaragozic acid A based on an acetal [1,2] Wittig rearrangement

(6) Tomooka, Katsuhiko a Kikuchi, Makoto a Igawa, Kazunobu a Suzuki, Masaki a Keong, Ping Huai a Nakai, Takeshi a

a TOKYO INSTITUTE OF TECHNOLOGY (Japan)

Author keywords

Asymmetric synthesis; Natural products; Rearrangements; Total synthesis

Indexed keywords

2,8 DIOXABICYCLO[3.2.1]OCTANE; ACETAL DERIVATIVE; BICYCLO COMPOUND; CARBON; LACTONE DERIVATIVE; NATURAL PRODUCT; UNCLASSIFIED DRUG; ZARAGOZIC ACID A;

ARTICLE; CHEMICAL BINDING; CHEMICAL STRUCTURE; CHIRALITY; NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; STEREOCHEMISTRY; SYNTHESIS;

EID: 0034671939 PISSN: 14337851 EISSN: None Source Type: Journal
DOI: 10.1002/1521-3773(20001215)39:24<4502::AID-ANIE4502>3.0.CO;2-K Document Type: Article

Times cited : (66)

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