A new reductone derived from D-glucuronolatone, 3-keto-4,5-dideoxy-trans-4,5-dehydroglucuronic acid.

DOI: 10.1248/cpb.11.1083

Source and publish data:

Chemical and pharmaceutical bulletin p. 1083 - 1084 (1963)

Update date:2022-08-02

Topics:

Authors:

Ishidate

Kimura Kimura

Kawata Kawata

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

Article abstract of DOI:10.1248/cpb.11.1083

Full text of DOI:10.1248/cpb.11.1083

NII-Electronic Library Service

Products guided by the article

Product name:4-phenylhydrazono-pentenedioic acid

Cas No:27847-33-2

R&D Labs maybe for 27847-33-2

Wuhan Benjamin Pharmaceutical Chemical Co.,Ltd

Contact:86-27-52341789

Address:Room 1518 B suite, optical valley time square, No 111 Guanshan Road, Hongshan District,Wuhan,Hubei Province,China.
SuZhou LaiTeou

Contact:+86-0512-88957371

Address:shanghai
Beijing Mashi Fine Chemical Co.,Ltd.

Contact:+86-10-61271592

Address:Room 506, Section B, Kaichi Mansion, Industrial Development
Hangzhou Gangjin Chemical Co.,Ltd.(expird)

Contact:+86-571-85109780

Address:707 Zhejiang Minhang Bldg., No.290 Zhongshan North Road, Hangzhou 310003, China
Jiangxi Global Natural Spice Co., Ltd.

website:https://www.jxhqxl.com/

Contact:+86-796-8106598

Address:No.89, Wenshan Road,South Industrial Park, Jishui County,Jiangxi Province

Relevant to this article

Synthesis of 7α-substituted derivatives of 17β-estradiol

Doi:10.1016/j.steroids.2005.11.008
(2006)
Tetraurea calix[4]arenes with sulfur functions: Synthesis, dimerization to capsules, and self-assembly on gold

Doi:10.1039/b616358k
(2007)
Synthesis of (-)-isofagomine

Doi:10.1080/07328300601039336
(2006)
Biosynthesis of naphthylisoquinoline alkaloids: synthesis and?incorporation of an advanced ¹³C₂-labeled isoquinoline?precursor

Doi:10.1016/j.tet.2006.12.022
(2007)
Exploring a new, connective Pummerer reaction: Formation of oxindoles by the reaction of thiols with glyoxamides

Doi:10.1039/b613591a
(2007)
Conjugated imines and iminium salts as versatile acceptors of nucleophiles

Doi:10.1039/b814930e
(2009)

Article Doi