Molecular species of Schiff bases derived from o hydroxyaromatic aldehydes. I. Spectral assignments

DOI: 10.1248/cpb.25.2568

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 2568 - 2575 (1977)

Update date:2022-08-05

Topics:

Authors:

Karube Karube

Matsushima

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

Article abstract of DOI:10.1248/cpb.25.2568

Full text of DOI:10.1248/cpb.25.2568

NII-Electronic Library Service

Products guided by the article

Product name:L-Tyrosine, N-[(3-hydroxy-4-pyridinyl)methylene]-, ethyl ester

Cas No:65481-98-3

R&D Labs maybe for 65481-98-3

Shanghai Sunway Pharmaceutical Technology Co.,Ltd.

Contact:+86-21-5161 3915

Address:Shanghai YangPu
Shandong Jiulong Hisince Pharmaceutical Co.,Ltd.

Contact:--

Address:Huadian Pioneer Park, Huadian Township, Qihe County, Dezhou City, Shandong, P.R.China
Chengdu Pukang Biotechnology Co., Ltd

website:http://www.pu-kang.com

Contact:86-028-63976226

Address:No. 868 Xiwang Road,Xinjin county,Chengdu city, China
Qingdao Pana-Life Biochem Co.,Ltd.

Contact:86-532-87683902

Address:No.967 Dalao Road, Licang Zone, Qingdao City,Shandong, China 266021
Jiaxing Taixin Pharmaceutical Chemical Co., Ltd

Contact:0573-82613601

Address:Chemical Park, Jiaxing, Zhejiang, China

Relevant to this article

Conversion of Amines into Phenylsulfides and Phenylselenides via Ditosylamides

Doi:10.1002/hlca.19800630806
(1980)
Synthesis of novel steroid-tetrahydroquinoline hybrid molecules and D-homosteroids by intramolecular cyclization reactions

Doi:10.1016/j.steroids.2004.01.004
(2004)
Organic Disulfides and Related Substances. 43. Properties of a Mercaptoalkyl Sulfoxide, a Novel Class of Structure

Doi:10.1021/jo00326a034
(1981)
Showdomycin analogues: Synthesis and antitumor evaluation

Doi:10.1021/jm00137a008
(1981)
A convenient formation of aporphine core via benzyne chemistry: Conformational analysis and synthesis of (R)-aporphine

Doi:10.1016/j.tetlet.2015.10.083
(2015)
Synthesis of modified Trichinella spiralis disaccharide epitopes and a comparison of their recognition by chemical mapping and saturation transfer difference NMR

Doi:10.1016/j.carres.2013.10.012
(2014)

Article Doi