SCOPUS 정보 검색 플랫폼

Journal of the American Chemical Society

Volumn 124, Issue 35, 2002, Pages 10435-10442

Stereoselective formal [3 + 3] cycloaddition approach to cis-1-azadecalins and synthesis of (-)-4a,8a-diepi-pumiliotoxin C. Evidence for the first highly stereoselective 6π-electron electrocyclic ring closures of 1-azatrienes

(6) Sklenicka, Heather M a Hsung, Richard P a McLaughlin, Michael J a Wei, Lin Li a Gerasyuto, Aleksey I a Brennessel, William B a

a UNIVERSITY OF MINNESOTA (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOADDITION APPROACH;

ELECTRONS; ISOMERS; STEREOCHEMISTRY; THERMODYNAMICS;

SYNTHESIS (CHEMICAL);

PUMILIOTOXIN; ALKALOID; ALKENE; AMPHIBIAN VENOM; DECALIN; HETEROCYCLIC COMPOUND; NAPHTHALENE DERIVATIVE; PUMILIOTOXIN C; QUINOLINE DERIVATIVE;

ARTICLE; ELECTRON TRANSPORT; REACTION ANALYSIS; ROTATION; STEREOCHEMISTRY; SYNTHESIS; THERMODYNAMICS; CHEMISTRY; CYCLIZATION; STEREOISOMERISM;

ALKALOIDS; ALKENES; AMPHIBIAN VENOMS; AZA COMPOUNDS; CYCLIZATION; NAPHTHALENES; STEREOISOMERISM; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.; QUINOLINES;

EID: 0037019536 PISSN: 00027863 EISSN: None Source Type: Journal
DOI: 10.1021/ja020698b Document Type: Article

Times cited : (113)

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