Im, DS Cheong, CS Lee, SH Youn, BH Kim, SC 2024-01-21T14:12:01Z 2024-01-21T14:12:01Z 2021-09-05 2000-03-03 0040-4020 https://pubs.kist.re.kr/handle/201004/141505 (+/-)-2-Cyano-2-phenyl-1-hexanol 3 was resolved to each enantiomer using Candida rugosa and Pseudomonas fluorescens lipases in 62 and 99% ee, respectively. The absolute stereochemistry of one of the enantiomers was determined to be (S) by diastereomeric amide formation and X-ray crystallography. The resolved alcohols of (R)- and (S)-isomer were transformed to Systhane(R) analogues. (C) 2000 Elsevier Science Ltd. All rights reserved. English PERGAMON-ELSEVIER SCIENCE LTD RESOLUTIONS ENANTIOMERS CARBON Chemoenzymatic synthesis of optically active 2-phenyl-2-(1H-1,2,4-triazol-1-ylmethyl)hexanenitrile Article 10.1016/S0040-4020(00)00031-4 1 TETRAHEDRON, v.56, no.10, pp.1309 - 1314 TETRAHEDRON 56 10 1309 1314 scie scopus 000085669200004 2-s2.0-0007094304 Chemistry, Organic Chemistry Article RESOLUTIONS ENANTIOMERS CARBON chemoenzymatic fungicide quaternary carbon lipase-catalyzed reaction