New methods and reagents in organic synthesis. 69. A new synthesis of alpha-amino acid and peptide amides of aromatic amines using a modified Curtius reaction with diphenyl phosphorazidate.

DOI: 10.1248/cpb.35.2698

Source and publish data:

Chemical and pharmaceutical bulletin p. 2698 - 2704 (1987)

Update date:2022-09-26

Topics:

Authors:

Shioiri Shioiri

Murata Murata

Hamada Hamada

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

Article abstract of DOI:10.1248/cpb.35.2698

Full text of DOI:10.1248/cpb.35.2698

Products guided by the article

Product name:[(S)-3-Methyl-1-(1-oxy-2-phenyl-quinolin-4-ylcarbamoyl)-butyl]-carbamic acid tert-butyl ester

Cas No:114684-58-1

R&D Labs maybe for 114684-58-1

Jitat Company Ltd

Contact:852-27701081

Address:Room 2509, New Tech Plaza, 34 Tai Yau St., San Po Kong, HK
Chongqing Shuangfeng Chemical Co.,Ltd

Contact:+86-23-49850156

Address:No.663,xuanhua Rd,yongchuan,chongqing,China
Shenzhen Hongyuan Import & Export Co., Ltd.

Contact:0755-26407171

Address:Shenzhen Hongyuan Chemical New Materials Technology Co., Ltd.
Jinan Hongfangde Pharmatech Co.LTD

Contact:0531-88870908

Address:F Bldg,750#,Shunhua Rd,New&High-tech Zone,Jinan,Shandong,China 250101
Golden Union Agrochemical Import and Export Co., Ltd.

Contact:86-755-23910527

Address:Room 1106, Tower 3A, Excellence Century Center, Futian District, Shenzhen, China

Relevant to this article

Further Rearrangement of Meisenheimer Products of Allyl Aryl Amine Oxides

Doi:10.1021/jo960647v
(1997)
An improved synthesis of isonitrosoacetanilides

Doi:10.1016/j.tetlet.2005.10.046
(2005)
Synthesis of sialoclusters appended to calix[4]arene platforms via multiple azide-alkyne cycloaddition. New inhibitors of hemagglutination and cytopathic effect mediated by BK and influenza A viruses

Doi:10.1039/b800598b
(2008)
Doi:10.1021/ja01853a013
(1941)
Reversal agent and linker variants of reversed chloroquines: Activities against Plasmodium falciparum

Doi:10.1021/jm900972u
(2010)
A versatile biosynthetic approach to amide bond formation

Doi:10.1039/c8gc01697f
(2018)

Article Doi