Acid-promoted rearrangement of drimane type epoxy compounds and their application in natural product synthesis

Chemical and Pharmaceutical Bulletin

Volumn 60, Issue 4, 2012, Pages 562-570

  Fujiwara, Naoko ^b   Kinoshita, Masako ^a   Uchida, Akira ^a   Ono, Machiko ^b   Kato, Keisuke ^a   Akita, Hiroyuki ^a,c  

^a TOHO UNIVERSITY   (Japan)

^b INTERNATIONAL UNIVERSITY OF HEALTH AND WELFARE   (Japan)

^c NIHON PHARMACEUTICAL UNIVERSITY   (Japan)

Author keywords

epoxy bicyclofarnesol; epoxy drimenol; epoxy drimenyl cyanide; (10S,7R) 7 acetoxy labda 8(17),13(14)E dien 15 ol; (9S) austrodoric acid; Acid promoted rearrangement

Indexed keywords

17BETA ACETOXY ENT LAMBDA DIEN 15 OL; ACID; ALLYL ALCOHOL; ALPHA EPOXYBICYCLOFARNESOL; ALPHA EPOXYDRIMENOL; ALPHA EPOXYDRIMENYLCYANIDE; AUSTRODORIC ACID; EPOXIDE; INDAN DERIVATIVE; KETOL; LEWIS ACID; NATURAL PRODUCT; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; COLUMN CHROMATOGRAPHY; DRUG STRUCTURE; DRUG SYNTHESIS; ENANTIOMER; MASS SPECTROMETRY; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; STRUCTURE ANALYSIS;

ACIDS; BIOLOGICAL AGENTS; EPOXY COMPOUNDS; MOLECULAR CONFORMATION; SESQUITERPENES; STEREOISOMERISM;

EID: 84859466441     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.60.562     Document Type: Article

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