Synthesis of 3,6-diaryl-1H-pyrazolo[3,4-b]pyridines via one-pot sequential Suzuki–Miyaura coupling-Reference-Cited by-同舟云学术

Synthesis of 3,6-diaryl-1H-pyrazolo[3,4-b]pyridines via one-pot sequential Suzuki–Miyaura coupling

Published:2018 Issue:61 Volume:8 Page:34883-34894
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Urvashi Urvashi¹²³⁴,Tandon Vibha⁵⁶⁷⁴^ORCID,Das Parthasarathi⁸⁹¹⁰⁴^ORCID,Kukreti S.¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry

2. University of Delhi

3. Delhi-110007

4. India

5. Special Centre for Molecular Medicine

6. Jawaharlal Nehru University

7. New Delhi-110067

8. Department of Applied Chemistry

9. Indian Institute of Technology (Indian School of Mines)

10. Dhanbad-826004

Abstract

An efficient method to produce diarylpyrazolo[3,4-b]pyridines derivatives via combination of chemoselective Suzuki–Miyaura cross-coupling reactions has been developed.

Funder

University Grants Commission

Department of Biotechnology, Ministry of Science and Technology

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/RA/C8RA07104G

Reference54 articles.

1. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds

2. Recent applications of the Suzuki–Miyaura cross-coupling reaction in organic synthesis

3. Transition-metal-catalyzed Suzuki–Miyaura cross-coupling reactions: a remarkable advance from palladium to nickel catalysts

4. Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions Employing Dialkylbiaryl Phosphine Ligands

5. Recent Developments in the Suzuki-Miyaura Reaction: 2010–2014

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