Quasi-biomimetic ring contraction promoted by a cysteine-based nucleophile: Total synthesis of Sch-642305, some analogs and their putative anti-HIV activities-Reference-Cited by-同舟云学术

Quasi-biomimetic ring contraction promoted by a cysteine-based nucleophile: Total synthesis of Sch-642305, some analogs and their putative anti-HIV activities

Published:2011 Issue:8 Volume:2 Page:1568
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Dermenci Alpay,Selig Philipp S.,Domaoal Robert A.,Spasov Krasimir A.,Anderson Karen S.,Miller Scott J.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2011/SC/C1SC00221J

Reference38 articles.

1. Isolation and Structure Elucidation of Sch 642305, a Novel Bacterial DNA Primase Inhibitor Produced by Penicillium verrucosum

2. Enantioselective total synthesis of bioactive natural product (+)-Sch 642305: a structurally novel inhibitor of bacterial DNA primase and HIV-1 Tat transactivation

3. Synthesis of (+)-Sch 642305 by a Biomimetic Transannular Michael Reaction

4. Stereoselective synthesis of Sch 642305, an inhibitor of bacterial DNA primase

5. Concise Synthesis of the Bacterial DNA Primase Inhibitor (+)-Sch 642305

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