Synthesis and chlorination of chloromethyl methylsulfonylmethyl sulfide

Terence Patrick Ahern; Tracy L. Hennigar; Justin Anthony MacDonald; Heather Grace Morrison; Richard Francis Langler; Satyendra Satyanarayana; Michael J. Zaworotko

doi:10.1071/C96143

Synthesis and chlorination of chloromethyl methylsulfonylmethyl sulfide

Terence Patrick Ahern
, Tracy L. Hennigar
, Justin Anthony MacDonald
, Heather Grace Morrison
, Richard Francis Langler
, Satyendra Satyanarayana
, Michael J. Zaworotko

Mount Allison University
Saint Mary's University Halifax

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

Abstract

A new cleavage reaction establishes rational access to the title compound. Treatment of the title compound with molecular chlorine establishes that methylsulfonyl is better than chloro as a directing group in the chlorination of unsymmetrical sulfides.

Original language	English
Pages (from-to)	683-687
Number of pages	5
Journal	Australian Journal of Chemistry
Volume	50
Issue number	6
DOIs	https://doi.org/10.1071/C96143
Publication status	Published - 1997
Externally published	Yes

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@article{6df0d3782d5241cca7567ee26dbf3191,

title = "Synthesis and chlorination of chloromethyl methylsulfonylmethyl sulfide",

abstract = "A new cleavage reaction establishes rational access to the title compound. Treatment of the title compound with molecular chlorine establishes that methylsulfonyl is better than chloro as a directing group in the chlorination of unsymmetrical sulfides.",

author = "Ahern, \{Terence Patrick\} and Hennigar, \{Tracy L.\} and MacDonald, \{Justin Anthony\} and Morrison, \{Heather Grace\} and Langler, \{Richard Francis\} and Satyendra Satyanarayana and Zaworotko, \{Michael J.\}",

year = "1997",

doi = "10.1071/C96143",

language = "English",

volume = "50",

pages = "683--687",

journal = "Australian Journal of Chemistry",

issn = "0004-9425",

number = "6",

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TY - JOUR

T1 - Synthesis and chlorination of chloromethyl methylsulfonylmethyl sulfide

AU - Ahern, Terence Patrick

AU - Hennigar, Tracy L.

AU - MacDonald, Justin Anthony

AU - Morrison, Heather Grace

AU - Langler, Richard Francis

AU - Satyanarayana, Satyendra

AU - Zaworotko, Michael J.

PY - 1997

Y1 - 1997

N2 - A new cleavage reaction establishes rational access to the title compound. Treatment of the title compound with molecular chlorine establishes that methylsulfonyl is better than chloro as a directing group in the chlorination of unsymmetrical sulfides.

AB - A new cleavage reaction establishes rational access to the title compound. Treatment of the title compound with molecular chlorine establishes that methylsulfonyl is better than chloro as a directing group in the chlorination of unsymmetrical sulfides.

UR - https://www.scopus.com/pages/publications/0009532312

U2 - 10.1071/C96143

DO - 10.1071/C96143

M3 - Article

AN - SCOPUS:0009532312

SN - 0004-9425

VL - 50

SP - 683

EP - 687

JO - Australian Journal of Chemistry

JF - Australian Journal of Chemistry

IS - 6

ER -

Synthesis and chlorination of chloromethyl methylsulfonylmethyl sulfide

Abstract

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