Recent Advances in Amino Acid-Based Phosphine Catalysts and Their Applications in Asymmetric Reactions
- Authors: Dan H.1,2, Rao G.1,2
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Affiliations:
- College of Pharmaceutical Science
- Institute of Drug Development and Chemical Biology
- Issue: Vol 54, No 6 (2018)
- Pages: 815-831
- Section: Review
- URL: https://bakhtiniada.ru/1070-4280/article/view/218028
- DOI: https://doi.org/10.1134/S1070428018060015
- ID: 218028
Cite item
Abstract
Amino acid-based catalysts have been intensively researched in recent years. Amino acid-derived phosphines possess high nucleophilicity and exhibit unique catalytic activities in asymmetric synthesis. L-Threonine and valine are most utilized natural amino acids in the preparation of chiral phosphines. The efficient and versatile chiral phosphine catalysts are applied in a wide range of reactions such as MBH reaction, Rauhut–Currier reaction, Michael addition, [4 + 2]-annulation, [3 + 2]-annulation, 1,4-dipolar cycloaddition. They are also widely used in the construction of core structures of natural products. Amino acid-based phosphine catalysts and their applications in asymmetric synthesis are summarized.
About the authors
Hu-Guang Dan
College of Pharmaceutical Science; Institute of Drug Development and Chemical Biology
Email: rgw@zjut.edu.cn
China, Hangzhou, 310014; Hangzhou, 310014
Guo-Wu Rao
College of Pharmaceutical Science; Institute of Drug Development and Chemical Biology
Author for correspondence.
Email: rgw@zjut.edu.cn
China, Hangzhou, 310014; Hangzhou, 310014
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