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Key Laboratory for Advanced Materials and Institute of Fine Chemicals, School of Chemistry & Molecular Engineering, East China University of Science and Technology, 130 Mei Long Road, Shanghai 200237, China
E-mail: zhangj@ecust.edu.cn
; Tel: +86 021 64252995
b
State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Road, Shanghai 200032, China
E-mail: mshi@mail.sioc.ac.cn
; Tel: +86 021 64252995
Chem. Commun., 2012,48, 9192-9194
DOI:
10.1039/C2CC34952C
Received
11 Jul 2012,
Accepted
26 Jul 2012
First published online
26 Jul 2012
We have found a Tf2O-mediated intramolecular cyclization reaction and have revealed an intriguing stereoselectivity and a regioselectivity during the preparation of intermediate alcohols, which allow for the tailor-made synthesis of various backbone-substituted imidazolinium salts, and structurally specific syn-4,5-disubstituted imidazolinium salts.
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