Smidt_1996_Biotechnol.Tech_10_335

Reference

Title : Preparation of optically pure chiral amines by lipase -catalyzed enantioselective hydrolysis of N-acyl-amines - Smidt_1996_Biotechnol.Tech_10_335
Author(s) : Smidt H , Fischer A , Fischer P , Schmid RD
Ref : Biotechnology Techniques , 10 :335 , 1996
Abstract :

A new and effective method using lipase from Candida antarctica (native or Novozym SP-435) for the preparation of enantiopure primary R-amines is reported. Hydrolysis of rac-N-acetyl-amines resulted in high conversion > 40% (168 hrs) and > 48 % (> 240 hrs) and enantiomeric excesses (> 99 %ee) for both the product and the remaining substrate

PubMedSearch : Smidt_1996_Biotechnol.Tech_10_335
PubMedID:
Gene_locus related to this paper: canar-LipB

Related information

Substrate Capsaicin
Gene_locus canar-LipB

Citations formats

Smidt H, Fischer A, Fischer P, Schmid RD (1996)
Preparation of optically pure chiral amines by lipase -catalyzed enantioselective hydrolysis of N-acyl-amines
Biotechnology Techniques 10 :335

Smidt H, Fischer A, Fischer P, Schmid RD (1996)
Biotechnology Techniques 10 :335