A new synthesis of biologically active pyrroles: Formal synthesis of pentabromopseudilin, bimetopyrol, and several antitubercular agents-Reference-Cited by-同舟云学术

A new synthesis of biologically active pyrroles: Formal synthesis of pentabromopseudilin, bimetopyrol, and several antitubercular agents

Published:2019-11-22 Issue:1 Volume:57 Page:327-336
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:J Heterocyclic Chem

Author:

Karimi Sasan¹^ORCID,Ma Shuai²,Qu Michelle¹,Chen Biling¹,Ramig Keith³,Greer Edyta M.³,Szalda David J.³,Neary Michelle C.⁴,Berkowitz William F.²,Subramaniam Gopal²

Affiliation:

1. Department of ChemistryQueensborough Community College of the City University of New York Bayside New York

2. Department of Chemistry and BiochemistryQueens College of the City University of New York Flushing New York

3. Department of Natural SciencesBaruch College of the City University of New York New York New York

4. Department of ChemistryHunter College of the City University of New York New York New York

Funder

American Chemical Society Petroleum Research Fund

Publisher

Wiley

Subject

Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jhet.3780

Reference71 articles.

1. Two-step total synthesis of an anti-MRSA and myosin-inhibiting marine natural product pentabromopseudilin via Suzuki-Miyaura coupling of a MIDA boronate ester

2. Silver(I)-Catalyzed Route to Pyrroles: Synthesis of Halogenated Pseudilins as Allosteric Inhibitors for Myosin ATPase and X-ray Crystal Structures of the Protein-Inhibitor Complexes

3. Synthesis of pentabromopseudilin and other arylpyrrole derivatives via Heck arylations

4. Total synthesis of biologically active alkaloids using transition metals

5. Total Synthesis of Pentabromo- and Pentachloropseudilin, and Synthetic Analogues-Allosteric Inhibitors of Myosin ATPase

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