Dynamic Kinetic Resolution Based Asymmetric Transfer Hydrogenation of α-Alkoxy-β-Ketophosphonates. Diastereo- and Enantioselective Synthesis of Monoprotected 1,2-Dihydroxyphosphonates-Reference-Cited by-同舟云学术

Dynamic Kinetic Resolution Based Asymmetric Transfer Hydrogenation of α-Alkoxy-β-Ketophosphonates. Diastereo- and Enantioselective Synthesis of Monoprotected 1,2-Dihydroxyphosphonates

Published:2014-03-06 Issue:6 Volume:79 Page:2666-2681
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Son Se-Mi¹²,Lee Hyeon-Kyu¹²

Affiliation:

1. Korea Chemical Bank, Korea Research Institute of Chemical Technology, PO Box 107, Yuseong, Daejeon 305-600, Korea

2. Department of Medicinal and Pharmaceutical Chemistry, University of Science and Technology, 113 Gwahango, Yuseong, Daejeon 305-333, Korea

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo500148j

Reference68 articles.

1. Diastereo- and Enantioselective Asymmetric Hydrogenation of α-Amido-β-keto Phosphonates via Dynamic Kinetic Resolution

2. Enantioselective Hydrogenation of β-Ketophosphonates with Chiral Ru(II) Catalysts

3. Synthesis and biological evaluation of phosphonate derivatives as autotaxin (ATX) inhibitors

4. New inhibitors of renin that contain novel phosphostatine Leu-Val replacements

5. The enantio- and diastereoselective synthesis of the first phospho-statine derivative

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