97189-64-5Relevant academic research and scientific papers
Monodisperse linear and cyclic oligo[(R)-3-hydroxybutanoates] containing up to 128 monomeric units
Lengweiler, Urs D.,Fritz, Monica G.,Seebach, Dieter
, p. 670 - 701 (2007/10/03)
Using benzyl ester/(tert-butyl)diphenylsilyl ether protection, (COCl)2/pyridine esterification conditions, and a fragment-coupling strategy (with H2/Pd-C debenzylation and HF-pyridine desilylation), linear oligomers of (R)-3-hydroxyb
BIOCHEMICAL PREPARATIONS OF BOTH THE ENANTIOMERS OF METHYL 3-HYDROXYPENTANOATE AND THEIR CONVERSION TO THE ENANTIOMERS OF 4-HEXANOLIDE, THE PHEROMONE OF TROGODERMA GLABRUM
Mori, Kenji,Mori, Hideto,Sugai, Takeshi
, p. 919 - 926 (2007/10/02)
Both the enantiomers of methyl 3-hydroxypentanoate were prepared by microbial asymmetric reduction of 3-oxopentanoic esters.Conversion of methyl 3-hydroxypentanoate to 4-hexanolide, the pheromone of Trogoderma glabrum, was achieved.
