Synfacts 2010(11): 1259-1259  
DOI: 10.1055/s-0030-1258797
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag Stuttgart ˙ New York

Stereospecific Substitution of Allylic Alcohols

Contributor(s): Mark Lautens, Jane Panteleev
M. Roggen, E. M. Carreira*
ETH Zürich, Switzerland
Further Information

Publication History

Publication Date:
21 October 2010 (online)

Significance

The authors disclose a stereo­specific allylic amination of optically active allylic alcohols using an iridium phosphoramidite catalyst and sulfamic acid as ammonia equivalent. An active iridium phosphoramidite complex is also isolated and characterized. Few examples of addition of free ammonia to primary allylic alcohols exist, but high ammonia equivalents and dilution are necessary to prevent overalkylation (T. Nagano, S. Kobayashi J. Am. Chem. Soc. 2009, 131, 4200; M. J. Pouy, L. M. Stanley, J. F. Hartwig J. Am. Chem. Soc. 2009, 131, 11312).