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 -