Protoilludane sesquiterpenes: synthesis of (±)-cerapicol, formal synthesis of (±)-sterpurene, and synthesis and absolute configuration of (+)-cerapicol-Reference-Cited by-同舟云学术

Protoilludane sesquiterpenes: synthesis of (±)-cerapicol, formal synthesis of (±)-sterpurene, and synthesis and absolute configuration of (+)-cerapicol

Published:2009-01 Issue:5 Volume:65 Page:1040-1047
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

El-Hachach Nizar,Gerke Ralf,Noltemeyer Mathias,Fitjer Lutz

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference73 articles.

1. Synthesis and rearrangement of [1,1′-bicyclobutyl]-1-ols and spiro[3.4]octan-5-ols: a general access to bicyclo[3.3.0]octenes (hexahydropentalenes)

2. Bioactive Sesquiterpenes Produced by Fungi are they Useful for Humans as Well

3. (+)-Sterpurene. Systematic name (Chemical Abstracts): (+)-(2aS,2bS,3aS)-2a,5,5,7-tetramethyl-2,2a,3,3a,4,5,6,7a-octahydro-1H-cyclobuta[f]indene. Isolation:

4. l-Sterpurene-3,12,14-triol and 1-sterpurene, metabolites of silver-leaf disease fungus Stereum purpureum

5. Studies on the biosynthesis of the sterpurenes

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2. Enantioselective Catalytic Aldehyde α‐Alkylation/Semipinacol Rearrangement: Construction of α‐Quaternary‐δ‐Carbonyl Cycloketones and Total Synthesis of (+)‐Cerapicol;Angewandte Chemie International Edition;2020-03-18

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