Enantioselective synthesis of unsaturated α-hydroxy acids
JA Macritchie, A Silcock, CL Willis
Index: Macritchie, Jacqueline A.; Silcock, Alan; Willis, Christine L. Tetrahedron Asymmetry, 1997 , vol. 8, # 23 p. 3895 - 3902
Full Text: HTML
Citation Number: 56
Abstract
(S)-and (R)-2-Hydroxyhex-5-enoic acid and (S)-and (R)-2-hydroxyhept-6-enoic acid were prepared in excellent yields and enantiomeric excesses (> 99% ee) from the corresponding α-keto esters by the enzyme catalysed hydrolysis of the ester and reduction of the ketone in a single pot process. The enantioselective synthesis of (S)-2-hydroxypent-4-enoic acid was achieved via reaction of the reagent derived from allyl bromide and indium metal with the ...
Related Articles:
[Fustero, Santos; Sanchez-Rosello, Maria; Sanz-Cervera, Juan F.; Acena, Jose Luis; Del Pozo, Carlos; Fernandez, Begona; Bartolome, Ana; Asensio, Amparo Organic Letters, 2006 , vol. 8, # 20 p. 4633 - 4636]
[Graham, Donald W.; Ashton, Wallace T.; Barash, Louis; Brown, Jeannette E.; Brown, Ronald D.; et al. Journal of Medicinal Chemistry, 1987 , vol. 30, # 6 p. 1074 - 1090]