Scholarly article on (2RS,3SR)-2-acetylamino-3-cyclohexyl-3-hydroxy-propionic acid ethyl ester 101172-62-7 from Bulletin of the Chemical Society of Japan p. 987,988

DOI: 10.1246/bcsj.29.987

Source and publish data:

Bulletin of the Chemical Society of Japan p. 987,988 (1956)

Update date:2022-07-30

Topics:

Authors:

Umezawa Umezawa

Oguma Oguma

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

Article abstract of DOI:10.1246/bcsj.29.987

Full text of DOI:10.1246/bcsj.29.987

Products guided by the article

Product name:(2RS,3SR)-2-acetylamino-3-cyclohexyl-3-hydroxy-propionic acid ethyl ester

Cas No:101172-62-7

R&D Labs maybe for 101172-62-7

Shandong LuZhou Amino Acid Co., Ltd

Contact:86-539-2218025

Address:yishui economic and technical development zone zhenxing south road
Zhangjiagang Golden Reach Fine Chemical Co.,LTD.

Contact:+86-512-6585 6968

Address:Changfu Road， Dongsha Chemical Industry Park, Zhangjiagang City, Jiangsu Province, China
shijiazhuang alkay chemicals co..ltd(expird)

Contact:86-311-67692035

Address:2601,juntang building,qiaodong district,shijiazhuang
ZK Biochem Group Co., Ltd

Contact:+86-532-80762375

Address:No. 6, Hongkong Middle Road, Qingdao, China
Sinoway International (Jiangsu) Co., Ltd.

Contact:+86-25-86630167

Address:17 Beijing Road (West), Nanjing, China

Relevant to this article

Preparation of a polymer-supported chiral 1,2-diamine and its application to the asymmetric hydrogenation of aromatic ketones

Doi:10.1016/j.tetasy.2007.12.002
(2008)
Semi-synthesis of polymyxin B (2-10) and colistin (2-10) analogs employing the trichloroethoxycarbonyl (Troc) group for side chain protection of α, γ-diaminobutyric acid residues

Doi:10.1248/cpb.55.1724
(2007)
Doi:10.1021/ja01561a037
(1957)
Doi:10.1021/ja01125a007
()
A simple route to enantiopure bis-lactones: synthesis of both enantiomers of epi-nor-canadensolide, nor-canadensolide, and canadensolide

Doi:10.1016/j.tet.2008.01.009
(2008)
Synthesis of novel macrocyclic crown ethers from D-glucose

Doi:10.1080/07328303.2016.1206115
(2016)

Article Doi

DOI: 10.1246/bcsj.29.987