Synfacts 2006(4): 0347-0347  
DOI: 10.1055/s-2006-934336
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag Stuttgart · New York

Sequential Pd-Catalyzed Asymmetric Allene Diboration/α-Aminoallylation

Contributor(s): Hisashi Yamamoto, Matthew B. Boxer
J. D. Sieber, J. P. Morken*
University of North Carolina at Chapel Hill, USA
Further Information

Publication History

Publication Date:
24 March 2006 (online)

Significance

This protocol utilizes the chiral diboron intermediate previously reported by this group as a ‘reagent’ for allylation of ammonia derived imines. Two methods can be used, often with similar yields and high chirality transfer. While the direct use of the aldehyde with NH4OAc is attractive and successful in many instances, the yields are significantly diminished when R1 = Cy and R2 = Ar. The authors were able to isolate the anticipated Z-intermediate from the reaction medium and performed an X-ray crystal structure analysis to identify the stereochemistry. The same intermediate was also used to show that the vinylborane could be applied in Suzuki-Miyaura cross-coupling reactions or simply protonated to form the disubstituted alkene.