Premium
Complete regioselective formation of 2‐(arylsulfinyl)diphenyl sulfides from 5‐arylthianthreniumyl perchlorates
Author(s) -
Kim Jongyup,
Kim Kab Sig,
Kim Kyongtae
Publication year - 1999
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570360307
Subject(s) - chemistry , regioselectivity , potassium , medicinal chemistry , sulfoxide , dimethyl sulfoxide , organic chemistry , catalysis
Treatment of 5‐arylthianthreniurnyl perchlorates with potassium tert ‐butoxide in dimethyl sulfoxide at room temperature gave 2‐(arylsulfinyl)diphenyl sulfides (29–79% yields), which are the first examples for complete regioselective formation of S ‐monoxides from unsymmetrical arylthiodiphenyl sulfides.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom