Synthesis of quaternary carbon-centered indolo[1,2-a]quinazolinones and indazolo[1,2-a]indazolones via C–H functionalization-Reference-Cited by-同舟云学术

Synthesis of quaternary carbon-centered indolo[1,2-a]quinazolinones and indazolo[1,2-a]indazolones via C–H functionalization

Published:2021 Issue:11 Volume:57 Page:1388-1391
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Gogoi Kongkona¹²³⁴⁵,Bora Bidisha R.¹²³⁴⁵,Borah Geetika⁶⁷⁸⁹^ORCID,Sarma Bipul¹⁰¹¹¹²⁹^ORCID,Gogoi Sanjib¹²³⁴⁵^ORCID

Affiliation:

1. Applied Organic Chemistry

2. Chemical Sciences & Technology Division

3. CSIR-North East Institute of Science and Technology

4. Jorhat-785006

5. AcSIR

6. Department of Chemistry

7. Dibrugarh University

8. Dibrugarh-786004

9. India

10. Department of Chemical Sciences

11. Tezpur University

12. Tezpur-784028

Abstract

A cascade, Ru(ii)-catalyzed annulative transformation of phenylindazolones and alkynes into indolo[1,2-a]quinazolinones and indazolo[1,2-a]indazolones is reported.

Funder

Science and Engineering Research Board

Department of Science and Technology, Ministry of Science and Technology

Council of Scientific and Industrial Research, India

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2021/CC/D0CC07419E

Reference33 articles.

1. Antimicrobial study of newly synthesized 6-substituted indolo[1,2-c]quinazolines

2. Analysis of stereoelectronic properties, mechanism of action and pharmacophore of synthetic indolo[2,1-b]quinazoline-6,12-dione derivatives in relation to antileishmanial activity using quantum chemical, cyclic voltammetry and 3-D-QSAR CATALYST procedures

3. Isolation, Structure Elucidation, and Synthesis of Cytotoxic Tryptanthrin Analogues from Phaius mishmensis

4. Evolution of Poly(ADP-ribose) Polymerase-1 (PARP-1) Inhibitors. From Concept to Clinic

5. Discovery of a Potent and Selective Protein Kinase CK2 Inhibitor by High-Throughput Docking

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