Stereoselective Introduction of Hydroxyl Groups via Hydrazones

DOI: 10.1246/bcsj.66.3532

Source and publish data:

Bulletin of the Chemical Society of Japan p. 3532 - 3533 (1993)

Update date:2022-08-03

Topics:

Authors:

Tada, Masahiro

Chiba, Kazuhiro

Izumiya, Koji

Tamura, Mihoko

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

Article abstract of DOI:10.1246/bcsj.66.3532

Reduction of tosylhydrazones by hydride reagents in wet alcohol gave predominantly alcohols whose stereochemistries are opposite to those of the major reduction products of the corresponding ketones with sodium borohydride.

Full text of DOI:10.1246/bcsj.66.3532

Products guided by the article

Product name:3,3,5-Trimethylcyclohexanon-tosylhydrazon

Cas No:41780-64-7

R&D Labs maybe for 41780-64-7

Zhejiang Kangfeng Chemical Co.,LTD.

Contact:+86-579-86709687

Address:Xueshizhai Industrial Zone, Weishan Town,Dongyang City, Zhejiang Province ,China
Phantom-pharma

Contact:

Address:
Oren Hydrocarbons (Qingdao) Co., Ltd.

Contact:+86-532-68607667-801

Address:Room 3 # 302, No.9 Qingyun Road, Qingdao, China
Henan zhongda Biological Engineering Co., Ltd

Contact:86-28-18109029985

Address:shenzhou road,xuedian industrial estate,zhengzhou city,henan province CHN
Hawks Chemical

Contact:+44 (0)161 367 9441

Address:

Relevant to this article

Doi:10.1016/0040-4020(78)89018-8
(1978)
Doi:10.1246/bcsj.52.524
(1979)
1,3-Dipolar cycloadditions of anhydro-5-hydroxyoxazolium hydroxide generated from 2-piperidinecarboxylic acid. Isolation of the primary adduct and synthesis of tetrahydroindolizines (1)

Doi:10.1002/jhet.5570150813
(1978)
Doi:10.1002/ardp.19793120213
(1979)
Doi:10.1016/0040-4020(78)89019-X
(1978)
Reactivity of (E)-4-aryl-4-oxo-2-butenoic acid phenylamides with piperidine and benzylamine: Kinetic and theoretical study

Doi:10.1007/s00706-014-1223-8
(2014)

Article Doi