Nucleophilic attack on 2,1-benzisothiazolium salts

DOI: 10.1139/v82-066

Source and publish data:

Canadian Journal of Chemistry p. 440 - 444 (1982)

Update date:2022-08-04

Topics: Organic compounds Nucleophilic Attack Electrophilic center

Authors:

McKinnon, David M.

Duncan, K. Ann

Millar, Lesley M.

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

Article abstract of DOI:10.1139/v82-066

2,1-benzisothiazolium salts react with several stabilized carbanions to give products that are derived by attack at the carbon atom of the heterocyclic ring.

Full text of DOI:10.1139/v82-066

Products guided by the article

Product name:[1-Phenyl-1H-benzo[c]isothiazol-(3Z)-ylidene]-pyridin-2-yl-acetic acid methyl ester

Cas No:81698-16-0

R&D Labs maybe for 81698-16-0

Shanghai Sungo Technology Chemical Co., Ltd

Contact:0086-21-51385579

Address:Room2010, F/20, Tonghua Plaza, NO 345 Jinxiang Road, Jinqiao Export Processing Zone, Shanghai, 201206 P.R.CHINA
Shandong Yuanli Science and Technology Co., Ltd.

Contact:86-0536-6777557

Address:Zhuliu Industiral Park,Changle County
BAODING SINO-CHEM INDUSTRY CO.,LTD

Contact:0312-5956088

Address:NO.8 FUXING ROAD,CHINA
Haitong Chemical Industrial Co.,Ltd.

website:https://www.haitonglongwin.com/

Contact:+86-022-66221018

Address:18-701, No.99, The 4th Street, TEDA,
Sarchem Laboratories, Inc.

Contact:732.938.2777

Address:5012 Industrial Road Farmingdale, NJ 07727

Relevant to this article

Anticonvulsant property of substituted 5-aryltetrazol-2-ylacetylcarbamides

Doi:10.1002/jhet.5570200321
(1983)
Antimalarial activity enhancement in hydroxymethylcarbonyl (HMC) isostere-based dipeptidomimetics targeting malarial aspartic protease plasmepsin

Doi:10.1016/j.bmc.2008.10.011
(2008)
Doi:10.1021/ja01117a040
(1953)
Solid-Phase Synthesis of Protected Peptides on a Polymer-Bound Oxime: Preparation of Segments Comprising the Sequence of a Cytotoxic 26-Peptide Analogue

Doi:10.1021/jo00138a011
(1982)
Catalytic asymmetric inverse-electron-demand oxa-diels-alder reaction of in situ generated ortho-quinone methides with 3-methyl-2-vinylindoles

Doi:10.1002/anie.201500215
(2015)
Aminooxazolinate; a chiral amidinate analogue

Doi:10.1039/b409113b
(2004)

Article Doi