SCOPUS 정보 검색 플랫폼

Volumn 51, Issue 3, 2015, Pages 565-568

An efficient route to highly enantioenriched tetrahydroazulenes and β-tetralones by desymmetrization reactions of δ,δ-diaryldiazoaceto-acetates

(5) Liu, Yuxiao a,b Deng, Yongming a Zavalij, Peter Y a Liu, Renhua b Doyle, Michael P a

a University of Maryland (United States)

b EAST CHINA UNIVERSITY OF SCIENCE AND TECHNOLOGY (China)

Author keywords

[No Author keywords available]

Indexed keywords

ACETIC ACID DERIVATIVE; AZULENE DERIVATIVE; BETA TETRALONE; CARBOXYLIC ACID; DELTA,DELTA DIARYLDIAZOACETO ACETATE; DIRHODIUM CARBOXYLATE; TETRAHYDROAZULENE; TETRALIN DERIVATIVE; UNCLASSIFIED DRUG; ACID; AZULENE; BETA-TETRALONE;

ARTICLE; CATALYSIS; CHEMICAL REACTION; CHIRALITY; CYCLOADDITION; DESYMMETRIZATION REACTION; ENANTIOSELECTIVITY; STEREOCHEMISTRY; CHEMICAL STRUCTURE; CHEMISTRY; CYCLIZATION; STEREOISOMERISM; X RAY CRYSTALLOGRAPHY;

ACETATES; ACIDS; AZULENES; CATALYSIS; CRYSTALLOGRAPHY, X-RAY; CYCLIZATION; MOLECULAR STRUCTURE; STEREOISOMERISM; TETRALONES;

EID: 84918563580 PISSN: 13597345 EISSN: 1364548X Source Type: Journal
DOI: 10.1039/c4cc08255a Document Type: Article

Times cited : (25)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.