Asymmetric Synthesis of α-Allyl-α-Aryl α-Amino Acids by Tandem Alkylation/π-Allylation of α-Iminoesters-Reference-Cited by-同舟云学术

Asymmetric Synthesis of α-Allyl-α-Aryl α-Amino Acids by Tandem Alkylation/π-Allylation of α-Iminoesters

Published:2014-03-25 Issue:7 Volume:16 Page:1948-1951
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Curto John M.¹,Dickstein Joshua S.¹,Berritt Simon¹,Kozlowski Marisa C.¹

Affiliation:

1. Department of Chemistry, Penn Merck High Throughput Experimentation Laboratory, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6323, United States

Funder

NIH Office of the Director

NSF Office of the Director

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol500506t

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1. Total Synthesis of Cyclic Tetrapeptide FR235222, a Potent Immunosuppressant that Inhibits Mammalian Histone Deacetylases

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4. Asymmetric Strecker-Type Reaction of α-Aryl Ketones. Synthesis of (S)-αM4CPG, (S)-MPPG, (S)-AIDA, and (S)-APICA, the Antagonists of Metabotropic Glutamate Receptors

5. Discovery of an Orally Active Non-Peptide Fibrinogen Receptor Antagonist

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