Sulfur extrusion from 1,4-benzothiazepines: Formation of 3-aryl-4-carbomethoxyisoquinolines

L. Fodor, David B. MacLean

Research output: Contribution to journalArticle

18 Citations (Scopus)

Abstract

Treatment of 3-aryl-2-carbomethoxy-4,5-dihydro-1 ,4-benzothiazepines with N-chlorosuccinimide in ether gave 3-aryl-4- carbomethoxyisoquinolines in a reaction in which the sulfur atom was extruded from the seven-membered thiazepin ring.

Original languageEnglish
Pages (from-to)18-20
Number of pages3
JournalCanadian Journal of Chemistry
Volume65
Issue number1
Publication statusPublished - Jan 1 1987

Fingerprint

Sulfur
Ether
Extrusion
Ethers
Atoms
N-chlorosuccinimide

ASJC Scopus subject areas

  • Chemistry(all)
  • Organic Chemistry
  • Catalysis

Cite this

Sulfur extrusion from 1,4-benzothiazepines : Formation of 3-aryl-4-carbomethoxyisoquinolines. / Fodor, L.; MacLean, David B.

In: Canadian Journal of Chemistry, Vol. 65, No. 1, 01.01.1987, p. 18-20.

Research output: Contribution to journalArticle

@article{513eb7421d884964957e945cf20426a0,
title = "Sulfur extrusion from 1,4-benzothiazepines: Formation of 3-aryl-4-carbomethoxyisoquinolines",
abstract = "Treatment of 3-aryl-2-carbomethoxy-4,5-dihydro-1 ,4-benzothiazepines with N-chlorosuccinimide in ether gave 3-aryl-4- carbomethoxyisoquinolines in a reaction in which the sulfur atom was extruded from the seven-membered thiazepin ring.",
author = "L. Fodor and MacLean, {David B.}",
year = "1987",
month = "1",
day = "1",
language = "English",
volume = "65",
pages = "18--20",
journal = "Canadian Journal of Chemistry",
issn = "0008-4042",
publisher = "National Research Council of Canada",
number = "1",

}

TY - JOUR

T1 - Sulfur extrusion from 1,4-benzothiazepines

T2 - Formation of 3-aryl-4-carbomethoxyisoquinolines

AU - Fodor, L.

AU - MacLean, David B.

PY - 1987/1/1

Y1 - 1987/1/1

N2 - Treatment of 3-aryl-2-carbomethoxy-4,5-dihydro-1 ,4-benzothiazepines with N-chlorosuccinimide in ether gave 3-aryl-4- carbomethoxyisoquinolines in a reaction in which the sulfur atom was extruded from the seven-membered thiazepin ring.

AB - Treatment of 3-aryl-2-carbomethoxy-4,5-dihydro-1 ,4-benzothiazepines with N-chlorosuccinimide in ether gave 3-aryl-4- carbomethoxyisoquinolines in a reaction in which the sulfur atom was extruded from the seven-membered thiazepin ring.

UR - http://www.scopus.com/inward/record.url?scp=0041533759&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0041533759&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:0041533759

VL - 65

SP - 18

EP - 20

JO - Canadian Journal of Chemistry

JF - Canadian Journal of Chemistry

SN - 0008-4042

IS - 1

ER -