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Electrochemically Induced Hetero‐[4+2]‐Cycloaddition Reactions Between 2‐Vinylpyrroles and β ‐Acceptor‐Substituted Enamines
Author(s) -
Peglow Thomas,
Blechert Siegfried,
Steckhan Eberhard
Publication year - 1998
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/(sici)1521-3765(199801)4:1<107::aid-chem107>3.0.co;2-e
Subject(s) - cycloaddition , chemistry , acceptor , electron transfer , electron acceptor , photochemistry , combinatorial chemistry , organic chemistry , catalysis , physics , condensed matter physics
An efficient route to indolizines is provided by radical‐cation‐initiated cycloaddition reactions between 2‐vinylpyrroles acting as heterodienes and enamines (below; SET = single electron transfer).