Reductive Alkylation of α-Keto Imines Catalyzed by PTSA/FeCl3: Synthesis of Indoles and 2,3′-Biindoles-Reference-Cited by-同舟云学术

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Reductive Alkylation of α-Keto Imines Catalyzed by PTSA/FeCl3: Synthesis of Indoles and 2,3′-Biindoles

Published:2015-06-05 Issue:12 Volume:80 Page:6381-6390
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Naidu P. Seetham¹,Kolita Sinki¹,Sharma Meenakshi¹,Bhuyan Pulak J.¹

Affiliation:

1. Medicinal Chemistry Division, CSIR-North East Institute of Science & Technology, Jorhat 785006, Assam, India

Funder

Department of Science and Technology, Ministry of Science and Technology

Council of Scientific and Industrial Research

University Grants Commission

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.5b00533

Reference76 articles.

1. Simple indole alkaloids and those with a nonrearranged monoterpenoid unit

2. Simple indole alkaloids and those with a non-rearranged monoterpenoid unit

3. The Combinatorial Synthesis of Bicyclic Privileged Structures or Privileged Substructures

4. Methods for drug discovery: development of potent, selective, orally effective cholecystokinin antagonists

5. Natural Product-like Combinatorial Libraries Based on Privileged Structures. 1. General Principles and Solid-Phase Synthesis of Benzopyrans

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