Scholarly article on bis-[2-(4-nitro-benzoyloxy)-ethyl]-disulfide 101732-49-4 from Journal of the American Chemical Society p. 838,840

DOI: 10.1021/ja01537a022

Source and publish data:

Journal of the American Chemical Society p. 838,840 (1958)

Update date:2022-08-05

Topics:

Authors:

Field Field

Lawson Lawson

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

Article abstract of DOI:10.1021/ja01537a022

Full text of DOI:10.1021/ja01537a022

Products guided by the article

Product name:bis-[2-(4-nitro-benzoyloxy)-ethyl]-disulfide

Cas No:101732-49-4

R&D Labs maybe for 101732-49-4

LinHai Cina Chemical Co., LTD.

Contact:0576-85580989

Address:Pharma-chem zone,Duqiao,Linhai,Zhejiang,China
Shanghai Norky Pharmaceutical Co., LTD.

website:http://www.norkypharm.com

Contact:86-21-61075300

Address:1165 Jiangning Road, Office 1502, Shanghai, China
LianYunGang Chiral Chemical(CHINA) CO.,LTD

Contact:+86-518-83616958 +86-519-82884848

Address:LianYunGang Chemical Industry Park (JiangSu)
Wuhan Shangrisyn chemicals Technology Co.,Ltd(expird)

Contact:+86-027-84466317 __ +86-15387123698

Address:wuhan - china
Jiangxi Lanqi Fine Chemical S&T Co., Ltd.

Contact:+86-21-64891143

Address:XinJiShan Industrial Area, Zhangshu City, JiangXi Province, China

Relevant to this article

One-Pot Electrochemical Nickel-Catalyzed Decarboxylative Sp²-Sp³ Cross-Coupling

Doi:10.1021/acs.orglett.8b04090
(2019)
Pentakis(trifluoromethyl)phenyl, a sterically crowded and electron-withdrawing group: Synthesis and acidity of pentakis(trifluoromethyl) benzene, -toluene, -phenol, and -aniline

Doi:10.1021/jo702513w
(2008)
Copper(II) bromide catalyzed novel preparation of propargylic ethers and sulfides by S_N1-type substitution between propargylic alcohols and alcohols or thiols

Doi:10.1055/s-2007-990951
(2008)
Facile rearrangement of N⁴-(α-aminoacyl)cytidines to N-(4-cytidinyl)amino acid amides

Doi:10.1016/j.tetlet.2008.02.015
(2008)
Doi:10.1002/hlca.19410240191
(1941)
Total Synthesis of (+)-MPC1001B

Doi:10.1002/anie.201507830
(2016)

Article Doi

DOI: 10.1021/ja01537a022