Diastereoselective reduction of α-keto amides having trans-2,5-disubstituted pyrrolidine as a chiral auxiliary

DOI: 10.1246/bcsj.62.3598

Source and publish data:

Bulletin of the Chemical Society of Japan p. 3598 - 3602 (1989)

Update date:2022-08-05

Topics:

Authors:

Kawanami

Fujita Fujita

Asahara Asahara

Katsuki Katsuki

Yamaguchi

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

Article abstract of DOI:10.1246/bcsj.62.3598

Full text of DOI:10.1246/bcsj.62.3598

Products guided by the article

Product name:(2R,5R)-N-<(2R)-2-hydroxy-2-phenylacetyl>-trans-2,5-bis(methoxymethoxymethyl)pyrrolidine

Cas No:115378-77-3

R&D Labs maybe for 115378-77-3

Changzhou Qidi Chemical Co., Ltd

website:http://www.czqdhg.com/

Contact:86-519-83382137

Address:128-1-16# HuaYuan Street,Hutang Town,Wujin District,Changzhou City,P.R.China.
Shanghai united Scientific Co.,Ltd.

Contact:+86-21-53535353

Address:28F No.900 huaihai Road Shanghai China
Shanghai Kangxin Chemical Co., Ltd

Contact:+86 21 60717227

Address:118,Ganbai Village,Waigang Town,Jiading District,Shanghai
Tianjin Tensing Fine Chemical Research Develop Centre

Contact:86-022-23718576,13032267585

Address:2-2-201,13 Guiyuan road,Huayuan Industry district,Tianjin,china
Dragon Chemical Co., Ltd.

Contact:0571-

Address:zhejing

Relevant to this article

A CONVENIENT SYNTHESIS OF 5-SUBSTITUTED-4-HYDROXY-3,4,5,6-TETRAHYDRO-2H-PYRAN-2-ONES VIA A CHEMOSELECTIVE DIFFERENTIATION OF THE TWO ESTER FUNCTIONS OF DIMETHYL ACETONEDICARBOXYLATE

Doi:10.1016/0040-4039(88)80010-8
(1988)
Organocatalytic syn-aldol reactions of dioxanones with (S)-isoserinal hydrate: Synthesis of L-deoxymannojirimycin and L-deoxyidonojirimycin

Doi:10.1021/jo900263s
(2009)
Para-Selective C-H Olefination of Aniline Derivatives via Pd/S,O-Ligand Catalysis

Doi:10.1021/jacs.9b01908
(2019)
Chemoselective reduction of quinoline over Rh-C60 nanocatalysts

Doi:10.1039/c9cy02025j
(2019)
STUDIES ON PILOCEREINE AND RELATED COMPOUNDS. III. SYNTHESIS OF

Doi:10.1248/cpb.11.1484
(1963)
Doi:10.1002/hlca.19620450658
(1962)

Article Doi