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Journal of the American Chemical Society

Volumn 123, Issue 19, 2001, Pages 4492-4501

Teubrevin G and teubrevin H: The first total syntheses of rearranged neo-clerodanes including solutions to the problems of chirality merger and furan ring assembly

(2) Paquette, L A a Efremov, I a

a OHIO STATE UNIVERSITY (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ENOLATES;

ADDITION REACTIONS; ALKYLATION; CATALYST SELECTIVITY; ISOMERS;

FURAN RESINS;

CLERODANE DERIVATIVE; DITERPENOID; ESTER DERIVATIVE; FURAN DERIVATIVE; TEUBREVIN G; TEUBREVIN H; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; CHEMICAL REACTION; CHIRALITY; DIASTEREOISOMER; SYNTHESIS;

CYCLIZATION; FURANS; MOLECULAR CONFORMATION; PLANTS; SPIRO COMPOUNDS; STEREOISOMERISM;

EID: 0034803612 PISSN: 00027863 EISSN: None Source Type: Journal
DOI: 10.1021/ja010313+ Document Type: Article

Times cited : (77)

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