THE PHILICITY OF PHENOXYCHLOROCARBENE TOWARD STYRENES

DOI: 10.1016/S0040-4039(00)88004-1

Source and publish data:

Tetrahedron Letters p. 2719 - 2722 (1983)

Update date:2022-08-03

Topics:

Authors:

Moss, Robert A.

Perez, Leon A.

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

Article abstract of DOI:10.1016/S0040-4039(00)88004-1

When generated by the thermolysis of 3-phenoxy-3-chlorodiazirine, phenoxychlorocarbene is an ambiphile in addition reactions with styrene derivatives.

Full text of DOI:10.1016/S0040-4039(00)88004-1

Products guided by the article

Product name:C₁₅H₁₃ClO

Cas No:344306-44-1

R&D Labs maybe for 344306-44-1

Shanghai He Yang International Trading Co., Ltd.

Contact:+86-21-52043598

Address:Room 816, Blag.5, No.58 Huachi Road
Shandong Yuanli Science and Technology Co., Ltd.

Contact:86-0536-6777557

Address:Zhuliu Industiral Park,Changle County
Chengdu Aslee Biopharmaceuticals, Inc

Contact:18608018419

Address:Chengdu Aslee Biopharmaceuticals, Inc
Hubei Lingsheng Pharmaceuticals Co., Ltd.

Contact:+86-0710-3538058

Address:Xiangyang City Xiangcheng Economic Development Zone, Hubei Province
Tianjin Hedong Red Cliff Chemical Reagent Factory

Contact:+86-022-84780548

Address:Li Ming Zhuang Gong Ye Yuan,Dongli District,Tianjin,China

Relevant to this article

Structure-Activity Relationships of Antibacterial 6,7- and 7,8-Disubstituted 1-Alkyl-1,4-dihydro-4-oxoquinoline-3-carboxylic Acids

Doi:10.1021/jm00186a014
(1980)
Reactions of 2-dialkylamino-5-phenyl-1,3-oxathiolium cation with nucleophiles containing an amino group

Doi:10.1248/cpb.26.3017
(1978)
New synthesis of all four 1-amino-2-hydroxycyclohexanecarboxylic acids

Doi:10.1016/S0040-4020(01)00129-6
(2001)
Doi:10.1007/BF00944410
()
Optimizing the Mizoroki–Heck reaction of cyclic allyl amines: Gram-scale synthesis of preclamol without protecting groups

Doi:10.1016/j.jcat.2018.01.007
(2018)
Slow shuttling in an amphiphilic bistable [2]rotaxane incorporating a tetrathiafulvalene unit

Doi:10.1002/1521-3773(20010401)40:7<1216::AID-ANIE1216>3.0.CO;2-W
(2001)

Article Doi