New Method for Synthesizing the Intermediates to 5-HETE from Yeast-mediated Reduction Products by Employing Baeyer-Villiger Oxidation with Complete Retention of Enantiomeric Excess
(R) and (S)-Aldehydes 2, which are intermediates for the synthesis of (5R) and (5S)-HETE, were respectively synthesized from the yeast-mediated reductive products, hydroxy ester 3 and cis-lactone 4, through Baeyer-Villiger oxidation with complete retention of enantiomeric excess.
GUINDON, YVAN;DELORME, DANIEL;LAU, CHEUK K.;ZAMBONI, ROBERT, J. ORG. CHEM., 53,(1988) N 2, 267-275
作者:GUINDON, YVAN、DELORME, DANIEL、LAU, CHEUK K.、ZAMBONI, ROBERT
DOI:——
日期:——
RAO, A. V. RAMA;REDDY, E. RAJARATHNAM;JOSHI, BHALCHANDRA V.;YADAV, J. S., TETRAHEDRON LETT., 28,(1987) N 51, 6497-6500
作者:RAO, A. V. RAMA、REDDY, E. RAJARATHNAM、JOSHI, BHALCHANDRA V.、YADAV, J. S.
DOI:——
日期:——
Simple efficient synthesis of LTB4 and 12-epi-LTB4
作者:Robert Zamboni、Joshua Rokach
DOI:10.1016/s0040-4039(00)87415-8
日期:1982.1
Synthesis of (R)-1-benzyloxy-3-buten-2-ol - a potential chiral synthon from L-(+)-tartaric acid: Its applications in natural product syntheses
作者:A V Rama Rao、E Rajarathnam Reddy、Bhalchandra V Joshi、J S Yadav
DOI:10.1016/s0040-4039(00)96898-9
日期:1987.1
A practical synthesis of (R)-3-butene-1,2-diol derivatives from (R,R)-tartaric acid and their applications for the syntheses of (R)-ethyl-5-benzoyloxy-5-formyl pentanoate (2), a useful synthon for the preparation of arachidonic acid metabolites and (R)-γ-caprolactone (3), a pheromone of Trogoderma species, are described.