Synthesis and antimicrobial activity of optically active trans-cycloheximide isomers

DOI: 10.1271/bbb1961.48.2315

Source and publish data:

Agricultural and Biological Chemistry p. 2315 - 2319 (1984)

Update date:2022-08-02

Topics:

Authors:

Kudo Kudo

Oritani Oritani

Yamashita

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

Article abstract of DOI:10.1271/bbb1961.48.2315

Full text of DOI:10.1271/bbb1961.48.2315

Products guided by the article

Product name:4-[(S)-2-((1S,3S,5S)-3,5-Dimethyl-2-oxo-cyclohexyl)-2-hydroxy-ethyl]-piperidine-2,6-dione

Cas No:5549-69-9

R&D Labs maybe for 5549-69-9

Shanghai ZaiQi Bio-Tech Co., Ltd.,

Contact:+86-21-5482 4098

Address:Bldg. No.7, No.201 MinYi Rd，Songjiang CaoHeJing High-Tech Park Shanghai 201516 P,R,China
Huzhou City Linghu Xinwang Chemical Co.,Ltd.

Contact:86-572-3948695/3945236

Address:huzhou
Hubei Danao Pharmaceutical Co.,Ltd.

website:http://www.danaopharm.com

Contact:+86-719-5251167

Address:Fandan Road,Danjiangkou,Hubei
Shanghai Dano Pharmaceutical Co.,Ld.(expird)

Contact:+86-592-6266840

Address:Building 1 Room 512, 720 Cailun Rd, Zhangjiang High-Tech Park, Shanghai 201203, China
SHANDONG ZHANHUA YONGHAO PHARMACEUTICAL TECH.CO.,LTD

Contact:+86-576-88685096

Address:GENGJU VILLAGE NORTH ONE KILOMETER,ZHANHUA DISTRICT,BINZHOU CITY,SHANDONG PROVINCE,CHINA.

Relevant to this article

Facile reduction of aromatic aldehydes, ketones, diketones and oxo aldehydes to alcohols by an aqueous TiCl₃/NH₃ system: Selectivity and scope

Doi:10.1002/1099-0690(200210)2002:19<3326::AID-EJOC3326>3.0.CO;2-V
(2002)
Doi:10.1016/S0040-4039(00)70286-3
(1959)
Doi:10.1039/c39750000207
()
Total synthesis of atroviridin

Doi:10.1016/S0040-4039(03)00629-4
(2003)
Substituent Effects and Stereochemistry in 125Te NMR Spectroscopy. Diorganyltellurium Dihalides and Some Tellurides and Ditellurides

Doi:10.1002/mrc.1260320509
(1994)
A facile and eco-friendly synthesis of imidazo[1,2-a]pyridines using nano-sized LaMnO₃ perovskite-type oxide as an efficient catalyst under solvent-free conditions

Doi:10.1016/j.apcata.2013.10.026
(2014)

Article Doi