Origin of Stereochemistry in the α-Amino Acid Esters and Amides Generated from Optically Active Zirconaaziridine Complexes1
Author:
Affiliation:
1. Contribution from the Department of Chemistry, Colorado State University, Fort Collins, Colorado 80523
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja953893h
Reference19 articles.
1. Williams has said that “asymmetric carboxylation [at the α position of an amine] is a surprisingly rarely studied approach [and] . a future area of investigation”. Williams, R. M.Synthesis of Optically Active α-Amino Acids; Pergamon: Oxford, 1989; Vol. 7.
2. Dipole stabilized α-amino carbanions. II. Alkylation of tetrahydroisoquinolines in the 1-position.
3. The preparation of carbon-11 labelled proline for positron emission tomography. Preliminary distribution studies in rats with walker 256 carcinosarcoma
4. Enantioselective electrophilic bond construction to the α-carbon of α-aminoacids
5. Complex Induced Proximity Effects: Enantioselective Syntheses Based on Asymmetric Deprotonations of N-Boc-pyrrolidines
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