Multifold C–C Coupling and Unorthodox Cyclization Catalysis for Selective Synthesis of Indolotriarylmethanes, Indolocarbazoles, and Their Analogues: A Control Experiment Study-Reference-Cited by-同舟云学术

Multifold C–C Coupling and Unorthodox Cyclization Catalysis for Selective Synthesis of Indolotriarylmethanes, Indolocarbazoles, and Their Analogues: A Control Experiment Study

Published:2016-12-23 Issue:1 Volume:82 Page:688-700
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Das Tuluma¹,Debnath Sudipto¹,Maiti Rituparna¹,Maiti Dilip K.¹^ORCID

Affiliation:

1. Department of Chemistry, University of Calcutta, 92 A. P. C. Road, Kolkata 700009, India

Funder

Council of Scientific and Industrial Research

University Grants Commission

Science and Engineering Research Board

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.6b02689

Reference72 articles.

1. First C−H Activation Route to Oxindoles using Copper Catalysis

2. Ruthenium(II)-Catalyzed C–H Bond Activation and Functionalization

3. Recent approaches for C–C bond formation via direct dehydrative coupling strategies

4. Iterative reactions of transient boronic acids enable sequential C–C bond formation

5. Water – the best solvent for DMAP-mediated dual cyclization towards metal-free first synthesis of fully substituted phthalimides

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