Part 1: Efficient strategies for the construction of variably substituted bicyclo[5.3.1]undecenones (AB taxane ring systems)

Canadian Journal of Chemistry

Volumn 82, Issue 2, 2004, Pages 215-226

  Laurent, Alain ^a,b   Villalva Servín, Nidia P ^a   Forgione, Pat ^a,c   Wilson, Peter D ^a,d   Smil, David V ^a,e   Fallis, Alex G ^a  

^a UNIVERSITY OF OTTAWA   (Canada)

^b Aegera Therapeutics   (Canada)

^c Boehringer Ingelheim   (Canada)

^d SIMON FRASER UNIVERSITY   (Canada)

^e METHYLGENE INC   (Canada)

Author keywords

Cycloaddition; Intramolecular Diels Alder; Lewis acid; Magnesium chelate

Indexed keywords

ADDITION REACTIONS; MOLECULAR DYNAMICS; OXYGEN; SUBSTITUTION REACTIONS;

CARBOMETALLATION; CYCLIC MOLECULES; CYCLOADDITIONS; LEWIS ACID;

COMPLEXATION;

ALCOHOL DERIVATIVE; BORON TRIFLUORIDE; BORON TRIFLUORIDE ETHERATE; DIETHYLALUMINUM CHLORIDE; LEWIS ACID; TAXANE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CARBOMETALLATION; CHEMICAL BOND; CHEMICAL MODIFICATION; CYCLOADDITION; DIASTEREOISOMER; DIELS ALDER REACTION; MOLECULE;

EID: 2342481147     PISSN: 00084042     EISSN: None     Source Type: Journal    
DOI: 10.1139/v03-200     Document Type: Article

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