Synfacts 2008(7): 0755-0755  
DOI: 10.1055/s-2008-1077815
Organo- and Biocatalysis
© Georg Thieme Verlag Stuttgart · New York

A New Phosphinothiourea Catalyst

Contributor(s): Benjamin List, Frank Lay
Y.-Q. Fang, E. N. Jacobsen*
Harvard University, Boston, USA
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Publikationsverlauf

Publikationsdatum:
20. Juni 2008 (online)

Significance

A new chiral bifunctional thiourea catalyst is introduced. Organocatalyst 1, derived from trans-2-amino-1-(diphenylphosphino)-cyclohexane and alanine, catalyzes the [3+2] cyclo­addition of imine 2 and allene 3 to substituted
2-aryl-2,5-dihydropyrroles 4 in good to high yields (68-90% yield) and high enantiomeric ratios (er = 97:3 up to 99:1). Both enantiomers of the aminophosphine precursor of catalyst 1 are prepared on a multi-gram scale by classical resolution.