Mapping the Pathway toward Thiophosphinic Pseudopeptides. Synthesis of Suitably Protected PG-Phe-Ψ[P(S)(OX)CH2]-Gly-OY Analogues as Thiophosphinyl Dipeptide Isosters (TDI), a Comparative Study for Selective Deprotection and Further Elongation-Reference-Cited by-同舟云学术

Mapping the Pathway toward Thiophosphinic Pseudopeptides. Synthesis of Suitably Protected PG-Phe-Ψ[P(S)(OX)CH2]-Gly-OY Analogues as Thiophosphinyl Dipeptide Isosters (TDI), a Comparative Study for Selective Deprotection and Further Elongation

Published:2013-10-02 Issue:20 Volume:78 Page:10069-10076
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Vassiliou Stamatia¹,Tzouma Eirini¹

Affiliation:

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

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo401084v

Reference25 articles.

1. Molecular Recognition of Protein−Ligand Complexes: Applications to Drug Design

2. Protease Inhibitors: Current Status and Future Prospects

3. New opportunities in drug design of metalloproteinase inhibitors: combination between structure–function experimental approaches and systems biology

4. Synthetic active site-directed inhibitors of metzincins: Achievement and perspectives

5. Phosphinic Pseudo-Tripeptides as Potent Inhibitors of Matrix Metalloproteinases: A Structure−Activity Study

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