SUBSTITUTION AND ADDITION REACTIONS OF ISOINDOLES

DOI: 10.1016/S0040-4020(01)91911-8

Source and publish data:

Tetrahedron p. 1401 - 1406 (1983)

Update date:2022-08-04

Topics:

Authors:

Bonnett, Raymond

North, Stephanie A.

Newton, Roger F.

Scopes, David I. C.

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

Article abstract of DOI:10.1016/S0040-4020(01)91911-8

1-Phenylisoindole reacts with toluene-p-diazonium chloride to give the azo derivative formed by electrophilic substitution at the free α position.However, attempted nitrosation of 1-phenylisoindole gave the product (3) of oxidative dimerisation, while the

Full text of DOI:10.1016/S0040-4020(01)91911-8

Products guided by the article

Product name:2-carbobenzyloxyisoindoline

Cas No:86557-80-4

R&D Labs maybe for 86557-80-4

Jiangyin Tenghua Import&Export Co.,Ltd.

Contact:+86-510-86263875

Address:Room 402-B,9 Yanling Road, Jiangyin,Jiangsu, China
Jiaxing Taixin Pharmaceutical Chemical Co., Ltd

Contact:0573-82613601

Address:Chemical Park, Jiaxing, Zhejiang, China
SINO GREAT ENTERPRISE LTD.

Contact:+86-731-84427351

Address:154 JIANXIANG SOUTH ROAD
Shanghai doly chemical Co.,Ltd

Contact:+86-21-34716221

Address:No.328,WuHe Roard,MinHang,ShangHai China
Regal(Guangzhou) Biology Technology CO., Ltd.

Contact:86-20-83528269

Address:Rm101,69th Tuan Jie Rd. Overseas Chinese Village G.Z. China

Relevant to this article

Enzymatic synthesis of novel chiral sulfoxides employing Baeyer-villiger monooxygenases

Doi:10.1002/ejoc.201000890
(2010)
Rhodium(II) Acetate-Catalysed Cyclization of Pyrazol-5-amine and 1,3-Diketone-2-diazo Compounds Using N,N-Dimethylformamide as a Carbon-Hydrogen Source: Access to Pyrazolo[3,4-b]pyridines

Doi:10.1002/adsc.201900093
(2019)
A novel synthesis of sulfuric acid mono-[2-(2-amino-ethanesulfonyl)-ethyl] ester for use as an intermediate in the preparation of reactive dyes

Doi:10.1081/SCC-120004152
(2002)
A Short and Efficient Synthesis of (-)-Ambrox<*> from (-)-Sclareol using a Ruthenium Oxide Catalyzed Key Step

Doi:10.1016/S0040-4039(00)61637-4
(1993)
Chlorination of p-substituted triarylpnictogens by sulfuryl chloride: Difference in the reactivity and spectroscopic characteristics between bismuth and antimony

Doi:10.1016/j.jorganchem.2005.06.040
(2005)
A novel method for asymmetric synthesis of both enantiomers of α-substituted carboxylic acid derivatives from optically active 1-chlorovinyl p-tolyl sulfoxides and lithium ester enolates with 1,4-chiral induction from the sulfur chiral center

Doi:10.1016/j.tetlet.2005.06.172
(2005)

Article Doi