Synthesis of Imidazo[2,1-b]thiazoles via Copper-Catalyzed A3-Coupling in Batch and Continuous Flow-Reference-Cited by-同舟云学术

Synthesis of Imidazo[2,1-b]thiazoles via Copper-Catalyzed A3-Coupling in Batch and Continuous Flow

Published:2017-08-25 Issue:18 Volume:82 Page:9682-9692
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Rassokhina Irina V.,Tikhonova Tatyana A.,Kobylskoy Sergey G.¹,Babkin Igor Yu.¹,Shirinian Valerii Z.^ORCID,Gevorgyan Vladimir²^ORCID,Zavarzin Igor V.,Volkova Yulia A.^ORCID

Affiliation:

1. Laboratory of High Technologies, Ltd, 86 prosp. Vernadskogo, 119571 Moscow, Russia

2. Department of Chemistry, University of Illinois at Chicago, 845 West Taylor Street, Room 4500, Chicago, Illinois 60607, United States

Funder

Russian Foundation for Basic Research

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.7b01762

Reference60 articles.

1. Design, synthesis and biological evaluation of imidazo[2,1-b]thiazole and benzo[d]imidazo[2,1-b]thiazole derivatives as Mycobacterium tuberculosis pantothenate synthetase inhibitors

2. A Decade of the Human Genome Sequence-How Does the Medicinal Chemist Benefit?

3. Discovery of Imidazo[2,1-b]thiazole HCV NS4B Inhibitors Exhibiting Synergistic Effect with Other Direct-Acting Antiviral Agents

4. The mechanism of action of the anthelmintic levamisole

5. Identification of N-(5-tert-Butyl-isoxazol-3-yl)-N′-{4-[7-(2-morpholin-4-yl-ethoxy)imidazo[2,1-b][1,3]benzothiazol-2-yl]phenyl}urea Dihydrochloride (AC220), a Uniquely Potent, Selective, and Efficacious FMS-Like Tyrosine Kinase-3 (FLT3) Inhibitor

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