Scholarly article on N6-benzyloxycarbonyl-N2-(2-phenyl-4,5-dihydro-oxazole-4-carbonyl)-L-lysine 27480-20-2 from Journal of the Chemical Society C: Organic p. 1610 - 1611

DOI: 10.1039/j39690001610

Source and publish data:

Journal of the Chemical Society C: Organic p. 1610 - 1611 (1969)

Update date:2022-08-03

Topics:

Authors:

Carpenter,J.G.

Moore,J.W.

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

Article abstract of DOI:10.1039/j39690001610

Full text of DOI:10.1039/j39690001610

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:N⁶-benzyloxycarbonyl-N²-(2-phenyl-4,5-dihydro-oxazole-4-carbonyl)-L-lysine

Cas No:27480-20-2

R&D Labs maybe for 27480-20-2

SINFACHEM LIMITED

Contact:86-25-84683399

Address:605, Phoenix Herui Plaza, No.389, South Taiping Road, Nanjing, China 210002
JIANGXI ZHANGFENG CHEMICAL CO., LTD.

Contact:+86-0799-3413066

Address:Xiyuan village, Xiabu Town, Xiangdong District
Taizhou Green Peptide Trading Co., Ltd.

Contact:--

Address:Room 1501, No71, Yuehe Road, Taizhou City, Zhejiang Province, China
Xi'an North Information Industry Co., Ltd. Weilv Chemical Department

Contact:+86-29-88156413

Address:Jixiang Road 99 Xi'an Shaanxi Province
Shanghai Rich Chemicals Co., Ltd

website:http://www.richchemical.com

Contact:+86-21-20255798

Address:Pudong Shanghai,China

Relevant to this article

Doi:10.1021/ja01167a010
(1950)
Nucleophilic substitution reactions of alcohols with use of montmorillonite catalysts as solid Bronsted acids

Doi:10.1021/jo070416w
(2007)
Synthesis and biological evaluation of disulfides bearing 1,2,4-triazole moiety as antiproliferative agents

Doi:10.1007/s00044-017-2029-0
(2017)
The 'non-oxidative' Pummerer reaction: Conclusive evidence for S(N)2- type stereoselectivity, mechanistic insight, and synthesis of enantiopure L- α-trifluoromethylthreoninate and D-α-trifluoromethyl-allo-threoninate

Doi:10.1021/jo991534p
(2000)
A new V-shaped organic fluorescent compound integrated with crystallization-induced emission enhancement and intramolecular charge transfer

Doi:10.1002/asia.201300331
(2013)
Cyclic 1,2-diketones as building blocks for asymmetric synthesis of cycloalkenones [8]

Doi:10.1021/ja000274m
(2000)

Article Doi

DOI: 10.1039/j39690001610