Diastereoselective addition of chlorotitanium enolate of N-acyl thiazolidinethione to O-methyl oximes: A novel, stereoselective synthesis of α,β-disubstituted β-amino carbonyl compounds via chiral auxiliary mediated azetine formation

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Liotta, D.C. (dliotta@emory.edu) | 1600年 / American Chemical Society卷 / 125期

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[1] Diastereoselective addition of chlorotitanium enolate of N-acyl thiazolidinethione to O-methyl oximes:: A novel, stereoselective synthesis of α,β-disubstituted β-amino carbonyl compounds via chiral auxiliary mediated azetine formation
Ambhaikar, NB
Snyder, JP
Liotta, DC
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (13) : 3690 - 3691
[2] Diastereoselective addition of chlorotitanium enolate of N-propionyl thiazolidinethione to O-methyl oximes.
Ambhaikar, NB
Liotta, DC
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2002, 224 : U260 - U260