1.
Biosci Biotechnol Biochem
; 80(8): 1459-63, 2016 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27023212
RESUMO
The first synthesis of the (9R,13R)-stereoisomer of LDS1, a flower-inducing oxylipin isolated from Lemna paucicostata, has been achieved from a known allylic alcohol by a seven-step sequence that involves the Horner-Wadsworth-Emmons olefination to construct its full carbon framework and an enzymatic hydrolysis of a penultimate methyl ester intermediate to provide the target molecule.