Enantioselective acetylation of an α-hydroxy ester by using ether-linked lipid-lipase aggregates in organic solvents

DOI: 10.1248/cpb.41.16

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 16 - 20 (1993)

Update date:2022-08-03

Topics:

Authors:

Akita Akita

Umezawa Umezawa

Tisnadjaja

Matsukura

Oishi Oishi

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1248/cpb.41.16

Phospholipids of a new type having ω-cyclohexyltridecyl groups were synthesized in order to investigate the influence of the structure of lipophilic part of phospholipids upon the enzymatic reaction. Enantioselective acetylation of an α-hydroxy ester was

Full text of DOI:10.1248/cpb.41.16

NII-Electronic Library Service

Products guided by the article

Product name:C₄₄H₇₈O₇

Cas No:149376-18-1

R&D Labs maybe for 149376-18-1

Beijing Tianjia Chemical Science & Technology Co.,Ltd

Contact:86-0550-2392698

Address:No.388, Shiliang Road (East),
Laohekou Jinghong Chemical Co.,Ltd

Contact:+86-0710-3702747

Address:163.East，Huagong Road，Laohekou
Synochem Ingredients Corp., Ltd.

Contact:+86-512-5636 2180

Address:Zhangjiagang Free Trade Zone
GenicBio Limited

Contact:+86-(0)21-3770 9035

Address:Room 301, Building 2, Meijiabang Road 1508, Shanghai China
Changzhou naidechemical Co.Ltd

Contact:+86-519-82589807

Address:NO.25,Houyang street,Jintan,Changzhou City

Relevant to this article

Organocatalyzed stereospecific C-C bond formation of β-lactams

Doi:10.1039/c3ob41858h
(2013)
A boron-oxygen transborylation strategy for a catalytic midland reduction

Doi:10.1021/acscatal.0c05168
(2021)
Enantioselective Synthesis of Chiral Amines via Biocatalytic Carbene N-H Insertion

Doi:10.1021/acscatal.0c02794
(2020)
Electron-transfer chain catalysis in phosphine replacement reaction: Determination of relative donor capability of arylpyridylphosphines

Doi:10.1016/j.ica.2006.12.051
(2007)
Doi:10.1021/jo01038a020
(1963)
Selective cleavage of the amido linkage of glucopyranosylamine derivatives by ion-exchange resin treatment

Doi:10.1248/cpb.32.3698
(1984)

Article Doi