Premium
A Convenient Synthesis of 2‐Aryl‐3‐per(poly) fluoroacylindoles
Author(s) -
Liu JinTao,
Liu HeJun
Publication year - 2002
Publication title -
chinese journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 41
eISSN - 1614-7065
pISSN - 1001-604X
DOI - 10.1002/cjoc.20020201129
Subject(s) - chemistry , aryl , cycloaddition , adduct , ionic bonding , fluorine , 1,3 dipolar cycloaddition , medicinal chemistry , combinatorial chemistry , polymer chemistry , organic chemistry , catalysis , ion , alkyl
2‐Aryl‐3‐per(poly) fluoroacylindoles were synthesized in good yields by the 1,3‐dipolar cycloaddition reaction of C‐aryl‐ N ‐phenylnitrones with fluorine‐containing olefins and the subsequent rearrangement of the adducts. An ionic mechanism was proposed for the formation of the titled compounds.
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