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Volumn 57, Issue 39, 2001, Pages 8243-8256

New entry to the synthesis of clerodane diterpenes. The first enantioselective syntheses of 7-oxo-kolavenic acid and methyl solidagonate

(11) Kato, Michiharu a Kosugi, Hiroshi a Ichiyanagi, Tsuyoshi a Hagiwara, Hisahiro b Kodaira, Ariko a Kusakari, Takashi a Suzuki, Takao a Ando, Minako a Lee, Jasmine a Drechsel, Peter c Vogler, Bernhard c

a TOHOKU UNIVERSITY (Japan)

b NIIGATA UNIVERSITY (Japan)

c UNIVERSITY OF HOHENHEIM (Germany)

Author keywords

Asymmetric synthesis; Cleavage reactions; Ene reactions; Natural products

Indexed keywords

4,8,8A TRIMETHYL 1,4A,5,6,8A PENTAHYDRONAPHTHALEN 2 ONE; 4,8,8A TRIMETHYLSPIRO(1',3' DIOXOLANE 2',7,1,4A,5,6,7,8,8A HEPTAHYDRONAPHTHTALEN) 2 ONE; 7 OXOKOLAVENIC ACID; ANTIINFLAMMATORY AGENT; CLERODANE DERIVATIVE; DITERPENE; ESTER DERIVATIVE; KETONE DERIVATIVE; METHYLSOLIDAGONIC ACID; NOPINONE; UNCLASSIFIED DRUG; VERBENONE;

ARTICLE; CHEMICAL REACTION; CHIRALITY; DRUG STRUCTURE; DRUG SYNTHESIS; ENANTIOMER; PRIORITY JOURNAL; REACTION ANALYSIS; STEREOCHEMISTRY; STEREOISOMERISM; STOICHIOMETRY;

EID: 0035944147 PISSN: 00404020 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4020(01)00821-3 Document Type: Article

Times cited : (9)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.