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Org Biomol Chem ; 15(17): 3756-3774, 2017 May 03.
Article in English | MEDLINE | ID: mdl-28406519

ABSTRACT

The Bi-[bmim][Br] combination has been found to offer high syn-selectivity in the crotylation of aldehydes with crotyl bromide using practically stoichiometric amounts of the reagents. The room temperature ionic liquid (RTIL), [bmim][Br], activated Bi metal in the presence of oxygen to produce crotylbismuthdibromide, which reacted with the aldehydes at room temperature. The major anti-syn diastereomeric product obtained from the crotylation of (R)-cyclohexylideneglyceraldehyde was utilized for the synthesis of dictyostatin and cryptophycin segments, and (+)-cis-aerangis lactone, using standard synthetic protocols.


Subject(s)
Aldehydes/chemistry , Aldehydes/chemical synthesis , Bismuth/chemistry , Imidazoles/chemistry , Organometallic Compounds/chemistry , Boronic Acids/chemistry , Chemistry Techniques, Synthetic , Lactones/chemistry , Stereoisomerism
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