Total synthesis of (R)-(+)-salsolidine by hydride addition to (R)-N-tert-butanesulfinyl ketimine

[1]  J. Ellman,et al.  One-pot asymmetric synthesis of either diastereomer of tert-butanesulfinyl-protected amines from ketones. , 2007, The Journal of organic chemistry.

[2]  Simona Chessa,et al.  An easy route to optically active 1-substituted-1-pyridyl-methylamines by diastereoselective reduction of enantiopure N-tert-butanesulfinyl ketimines , 2006 .

[3]  D. Morton,et al.  Chiral non-racemic sulfinimines: versatile reagents for asymmetric synthesis , 2006 .

[4]  F. A. Davis.  Adventures in sulfur-nitrogen chemistry. , 2006, The Journal of organic chemistry.

[5]  M. Faul,et al.  Reversal of diastereofacial selectivity in hydride reductions of N-tert-butanesulfinyl imines. , 2006, The Journal of organic chemistry.

[6]  Yong Qin,et al.  Selective diethylzinc reduction of imines in the presence of ketones catalyzed by Ni(acac)2. , 2006, Organic letters.

[7]  M. Rozwadowska,et al.  Diastereoselective Pomeranz–Fritsch–Bobbitt synthesis of (S)-(−)-salsolidine using (R)-N-tert-butanesulfinylimine as a substrate , 2006 .

[8]  M. Chrzanowska,et al.  Synthesis of (S)-(−)- and (R)-(+)-O-methylbharatamine using a diastereoselective Pomeranz–Fritsch–Bobbitt methodology , 2005 .

[9]  Salvatore Baldino,et al.  Asymmetric synthesis of 1-substituted-1-(pyridin-2-yl)methylamines by diastereoselective reduction of enantiopure N-p-toluenesulfinyl ketimines , 2005 .

[10]  J. Ellman,et al.  N-sulfinyl metalloenamine conjugate additions: asymmetric synthesis of piperidines. , 2005, The Journal of organic chemistry.

[11]  J. Ellman,et al.  Asymmetric α-Alkylation of N‘-tert-Butanesulfinyl Amidines. Application to the Total Synthesis of (6R,7S)-7-Amino-7,8-dihydro-α-bisabolene , 2004 .

[12]  A. Głuszyńska,et al.  Enantioselective addition of methyllithium to a prochiral imine—the substrate in the Pomeranz–Fritsch–Bobbitt synthesis of tetrahydroisoquinoline derivatives mediated by chiral monooxazolines , 2004 .

[13]  F. A. Davis,et al.  Recent Advances in Asymmetric Reactions Using Sulfinimines (N-Sulfinyl Imines) , 2004 .

[14]  J. Ellman,et al.  Development and application of a new general method for the asymmetric synthesis of syn- and anti-1,3-amino alcohols. , 2003, Journal of the American Chemical Society.

[15]  J. Ellman,et al.  Applications of tert-butanesulfinamide in the asymmetric synthesis of amines , 2003 .

[16]  J. Ellman,et al.  N-tert-butanesulfinyl imines: versatile intermediates for the asymmetric synthesis of amines. , 2002, Accounts of chemical research.

[17]  J. Ellman,et al.  Asymmetric synthesis of syn- and anti-1,3-amino alcohols. , 2002, Journal of the American Chemical Society.

[18]  R. Pedrosa,et al.  A novel straightforward synthesis of enantiopure tetrahydroisoquinoline alkaloids. , 2001, The Journal of organic chemistry.

[19]  A. Głuszyńska,et al.  Enantioselective modification of the Pomeranz–Fritsch–Bobbitt synthesis of tetrahydroisoquinoline alkaloids synthesis of (−)-salsolidine and (−)-carnegine , 2000 .

[20]  J. Ellman,et al.  One-pot asymmetric synthesis of tert-butanesulfinyl-protected amines from ketones by the in situ reduction of tert-butanesulfinyl ketimines , 1999 .

[21]  J. Ellman,et al.  Synthesis of Enantiomerically Pure N-tert-Butanesulfinyl Imines (tert-Butanesulfinimines) by the Direct Condensation of tert-Butanesulfinamide with Aldehydes and Ketones , 1999 .

[22]  David R. J. Hose,et al.  Asymmetric synthesis of amines using a chiral, non-racemic, benzylidene sulfinamide derived from a recoverable precursor , 1996 .