Straightforward and Diastereoselective Synthesis of Tetrafunctionalized Thiol Synthons for the Design of Metallopeptidase Inhibitors-Reference-Cited by-同舟云学术

Straightforward and Diastereoselective Synthesis of Tetrafunctionalized Thiol Synthons for the Design of Metallopeptidase Inhibitors

Published:2000-01 Issue:2 Volume:56 Page:209-215
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

David Christelle,Bischoff Laurent,Roques Bernard P,Fournié-Zaluski Marie-Claude

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference21 articles.

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2. Differential Inhibition of Aminopeptidase A and Aminopeptidase N by New .beta.-Amino Thiols

3. Design of novel inhibitors of aminopeptidases. Synthesis of peptide-derived diamino thiols and sulfur replacement analogs of bestatin

4. 2,4-Dinitrophenyl 4-Methoxybenzyl Disulfide: A New Efficient Reagent for the Electrophilic Sulfenylation of β-Amino Ester Enolates

5. .alpha.-Alkylation of alkyl alkanesulfonates

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