Separation and Identification of Residual Diastereomers in a Maximally Labeled Triarylamine

DOI: 10.1021/ja00528a044

Source and publish data:

Journal of the American Chemical Society p. 2777 - 2786 (1980)

Update date:2022-08-04

Topics:

Authors:

Glaser, Robert

Blount, John F.

Mislow, Kurt

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

Article abstract of DOI:10.1021/ja00528a044

Residual diastereoisomerism in a maximally labeled triarylamine, methyl N-(biphenyl-2-yl)-N-(1-naphthyl)anthranilate, has been demonstrated for the first time.The two stereoisomers were obtained by manual separation of crystals, and their structures were

Full text of DOI:10.1021/ja00528a044

Products guided by the article

Product name:methyl N-(biphenyl-2-yl)-N-(1-naphthyl)anthranilate

Cas No:74531-52-5

R&D Labs maybe for 74531-52-5

zhangjiagang bonded areas banggao co;ltd

website:http://www.shunchangchem.com

Contact:0086-13921972933

Address:Dongsha Chemical Zone.Zhangjiagang, Jiangsu Province
ChangZhou XiaQing Chemical Co., Ltd.

Contact:+86-519-88721665

Address:3# Hengluo Road, Henglin Town, Changzhou City, Jiangsu Province，China
Wuhan Konberd Biotech Co., Ltd.

Contact:+86-27-87205925

Address:NO.666, Gaoxin Road, Eastlake High-tech zone
JIANGXI ZHANGFENG CHEMICAL CO., LTD.

Contact:+86-0799-3413066

Address:Xiyuan village, Xiabu Town, Xiangdong District
Jiangsu Allyrise Pharmaceutical Co., Ltd.(expird)

Contact:+86-523-86818997

Address:Taizhou,Jiangsu Province,CHINA

Relevant to this article

Doi:10.1021/ja01627a076
(1955)
The Chemical Constituents of Australian Zanthoxylum Species. VII. Some Transformation Products of Suberosin

Doi:10.1071/CH9800395
(1980)
Doi:10.1021/ja01591a056
(1956)
Studies on peptides. XCIV. Synthesis and activity of kyotorphin and its analogs

Doi:10.1248/cpb.28.1935
(1980)
Nanomagnetically modified vitamin B₃ (Fe₃O₄@Niacin): An efficient and reusable green biocatalyst for microwave-assisted rapid synthesis of 2-amino-3-cyanopyridines in aqueous medium

Doi:10.1002/aoc.4103
(2018)
A New, Elegant Route to a Key Intermediate for the Synthesis of 9(O)-Methanoprostacyclin

Doi:10.1021/jo01311a047
(1980)

Article Doi