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-Reference-Cited by-同舟云学术

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

Published:2003-03-08 Issue:13 Volume:125 Page:3690-3691
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Ambhaikar Narendra B.¹,Snyder James P.¹,Liotta Dennis C.¹

Affiliation:

1. Department of Chemistry, Emory University, Atlanta, Georgia 30322

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja029871u

Reference18 articles.

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2. Acyclic stereoselection. 48. Reversal of stereochemistry in the aldol reactions of a chiral boron enolate

3. Chiral Induction Using Heterocycles

4. For a review: Cherry, P. C.; Newall, C. E. InChemistry and Biology ofβ-Lactam Antibiotics; Morin, R. B., Gorman, M., Eds.; Academic: New York, 1982; Vol. 2, p 361. Maryanoff, B. E.; Greco, M. N.; Zhang, H. C.; Andrade-Gordon, P.; Kaufman, J. A.; Nicolaou, K. C.; Liu, A.; Grugs, P. H.J. Am. Chem. Soc.1995,117, 1225.

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