Highly Enantioselective Asymmetric Isomerization of Primary Allylic Alcohols with an Iridium–N, P Complex
JQ Li, B Peters, PG Andersson
Index: Li, Jia-Qi; Peters, Byron; Andersson, Pher G. Chemistry - A European Journal, 2011 , vol. 17, # 40 p. 11143 - 11145
Full Text: HTML
Citation Number: 1
Abstract
The asymmetric transformation of allylic amines to optically active enamines, catalyzed by rhodium-BINAP complexes, has been well studied and even applied in industry.[1] The related transition-metal-catalyzed isomerization of primary allylic alcohols is an atom- economical route to the corresponding aldehydes (Scheme1). Various catalysts have been developed for this reaction,[2] however, only a few asymmetric examples have been ...
Related Articles:
[Dawson, Glenn W.; Pickett, John A.; Smiley, Diane W. M. Bioorganic and Medicinal Chemistry, 1996 , vol. 4, # 3 p. 351 - 361]
[Tetrahedron Letters, , vol. 47, # 42 p. 7417 - 7421]
[Kanazawa, Yoshinori; Nishiyama, Hisao Synlett, 2006 , # 19 p. 3343 - 3345]
[Akagawa, Kengo; Akabane, Hajime; Sakamoto, Seiji; Kudo, Kazuaki Tetrahedron Asymmetry, 2009 , vol. 20, # 4 p. 461 - 466]
[Chapuis, Christian; Barthe, Michel; Laumer, Jean-Yves de Saint Helvetica Chimica Acta, 2001 , vol. 84, # 1 p. 230 - 242]