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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.