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Titanium‐Mediated Domino Radical Cyclization/β Elimination of Phosphine Oxides
Author(s) -
Leca Dominique,
Fensterbank Louis,
Lacôte Emmanuel,
Malacria Max
Publication year - 2004
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.200460099
Subject(s) - domino , phosphine , domino effect , chemistry , radical cyclization , phosphine oxide , medicinal chemistry , combinatorial chemistry , organic chemistry , political science , catalysis , law
A phosphinoyl radical leaving group in the β position is a key feature of a new Ti III ‐mediated domino radical cyclization/β elimination reaction of vinylic phosphine oxides, which affords alkylidenepyrrolidines in good yields (see scheme).