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Organic and Biomolecular Chemistry

Volumn 4, Issue 23, 2006, Pages 4292-4298

Efficient and highly enantioselective formation of the all-carbon quaternary stereocentre of lyngbyatoxin A

(2) Vital, Paulo a Tanner, David a

a TECHNICAL UNIVERSITY OF DENMARK (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOLS; MOLECULAR STRUCTURE; PHASE TRANSITIONS; REACTION KINETICS; SYNTHESIS (CHEMICAL);

HEMETSBERGER KNITTEL REACTION; INDOLES; LYNGBYATOXIN; VINYL EPOXIDES;

NITROGEN COMPOUNDS;

INDOLE DERIVATIVE; LYNGBYATOXIN;

ARTICLE; CHEMISTRY; CYANOBACTERIUM; STEREOISOMERISM; SYNTHESIS;

CYANOBACTERIA; INDOLES; LYNGBYA TOXINS; STEREOISOMERISM;

EID: 33750974445 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/b612578f Document Type: Article

Times cited : (15)

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