Regioselective Suzuki–Miyaura reactions of 4,7-dichloro-N-methylisatin. Synthesis, anti-HIV activity and modeling study-Reference-Cited by-同舟云学术

Regioselective Suzuki–Miyaura reactions of 4,7-dichloro-N-methylisatin. Synthesis, anti-HIV activity and modeling study

Author:

Hamdy Aws M.¹²³⁴⁵,Al-Masoudi Najim A.⁵⁶⁷⁸⁹,Pannecouque Christophe¹⁰¹¹¹²¹³¹⁴,Rahman Qamar¹²³⁴¹⁵,Villinger Alexander¹²³⁴,Langer Peter¹²³⁴¹⁶

Affiliation:

1. Institut für Chemie

2. Universität Rostock

3. 18059 Rostock

4. Germany

5. Department of Chemistry

6. College of Science

7. University of Basrah

8. Basrah

9. Iraq

10. KU Leuven

11. Department of Microbiology and Immunology

12. Laboratory of Virology and Chemotherapy

13. Rega Institute for Medical Research

14. B-3000 Leuven

15. Amity University

16. Leibniz-Institut für Katalyse e. V. an der Universität Rostock

Abstract

Suzuki–Miyaura reactions of 4,7-dichloro-N-methylisatin provide a convenient access to arylated methylisatins.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

Reference39 articles.

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