Catalytic Enantioselective Formation of C−C Bonds by Addition to Imines and Hydrazones: A Ten-Year Update
Author:
Affiliation:
1. Department of Chemistry, School of Science, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-0033, Japan
2. School of Chemistry, University of Birmingham, Edgbaston, Birmingham B15 2TT, U.K.
Publisher
American Chemical Society (ACS)
Subject
General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/cr100204f
Reference664 articles.
1. Recent Developments in the Catalytic Asymmetric Synthesis of α- and β-Amino Acids
2. Recent advances in the stereoselective synthesis of β-amino acids
3. Recent developments in the stereoselective synthesis of α-aminoacids
4. Recent Advances in Natural Product Synthesis by Using Intramolecular Diels−Alder Reactions
5. Tandem Diels−Alder Cycloadditions in Organic Synthesis
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