Late-Stage Diversification of Phosphinic Dehydroalanine Pseudopeptides Based on a Giese-Type Radical C-Alkylation Strategy-Reference-Cited by-同舟云学术

Late-Stage Diversification of Phosphinic Dehydroalanine Pseudopeptides Based on a Giese-Type Radical C-Alkylation Strategy

Published:2019-04-01 Issue:12 Volume:21 Page:4397-4401
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Voreakos Kostas¹,Devel Laurent²^ORCID,Georgiadis Dimitris¹^ORCID

Affiliation:

1. Department of Chemistry, Laboratory of Organic Chemistry, National and Kapodistrian University of Athens, Panepistimiopolis, Zografou, 15771 Athens, Greece

2. CEA, Institut des Sciences du Vivant Frédéric Joliot, Service d’Ingénierie Moléculaire des Protéines (SIMOPRO), Université Paris-Saclay, Gif-sur-Yvette 91190, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b00857

Reference49 articles.

1. Phosphinic Peptides as Potent Inhibitors of Zinc-Metalloproteases

2. Remarkable Potential of the α-Aminophosphonate/Phosphinate Structural Motif in Medicinal Chemistry

3. Phosphinic peptides as zinc metalloproteinase inhibitors

4. Phosphinic acids: current status and potential for drug discovery

5. A new transcriptional role for matrix metalloproteinase-12 in antiviral immunity

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