2-Methylsulfanylbenzo[f]isoquinoline

Faisal Jamshaid; Musharraf Khan; Karl Hemming

doi:10.3390/M860

2-Methylsulfanylbenzo[f]isoquinoline

Faisal Jamshaid, Musharraf Khan, Karl Hemming

Research output: Contribution to journal › Article › peer-review

1 Citation (Scopus)

Abstract

S-Methylation of a 4-(naphth-2-yl)-β-thiolactam gives an intermediate 4-(naphth-2-yl) substituted 1-azetine which undergoes a [2+2] ring-opening followed by electrocyclic ring closure of the resulting 2-azadiene to give a benzo[f]isoquinoline.

Original language	English
Pages (from-to)	M860
Number of pages	5
Journal	MolBank
Volume	2015
Issue number	2
Early online date	27 May 2015
DOIs	https://doi.org/10.3390/M860
Publication status	Published - 1 Jun 2015

Access to Document

10.3390/M860Licence: CC BY

Cite this

@article{9f5b6e278ef646d49aeb33c089f9a9de,

title = "2-Methylsulfanylbenzo[f]isoquinoline",

abstract = "S-Methylation of a 4-(naphth-2-yl)-β-thiolactam gives an intermediate 4-(naphth-2-yl) substituted 1-azetine which undergoes a [2+2] ring-opening followed by electrocyclic ring closure of the resulting 2-azadiene to give a benzo[f]isoquinoline.",

keywords = "benzoisoquinoline, 1-azetine, naphthalene",

author = "Faisal Jamshaid and Musharraf Khan and Karl Hemming",

year = "2015",

month = jun,

day = "1",

doi = "10.3390/M860",

language = "English",

volume = "2015",

pages = "M860",

journal = "MolBank",

issn = "1422-8599",

publisher = "Multidisciplinary Digital Publishing Institute (MDPI)",

number = "2",

}

TY - JOUR

T1 - 2-Methylsulfanylbenzo[f]isoquinoline

AU - Jamshaid, Faisal

AU - Khan, Musharraf

AU - Hemming, Karl

PY - 2015/6/1

Y1 - 2015/6/1

N2 - S-Methylation of a 4-(naphth-2-yl)-β-thiolactam gives an intermediate 4-(naphth-2-yl) substituted 1-azetine which undergoes a [2+2] ring-opening followed by electrocyclic ring closure of the resulting 2-azadiene to give a benzo[f]isoquinoline.

AB - S-Methylation of a 4-(naphth-2-yl)-β-thiolactam gives an intermediate 4-(naphth-2-yl) substituted 1-azetine which undergoes a [2+2] ring-opening followed by electrocyclic ring closure of the resulting 2-azadiene to give a benzo[f]isoquinoline.

KW - benzoisoquinoline

KW - 1-azetine

KW - naphthalene

U2 - 10.3390/M860

DO - 10.3390/M860

M3 - Article

VL - 2015

SP - M860

JO - MolBank

JF - MolBank

SN - 1422-8599

IS - 2

ER -