Chemoselective Divergent Transformations of <i>N</i>-(Propargyl)indole-2-carbonitriles with Nitrogen Nucleophiles: Alkyne Hydroamination or Domino Cyclizations-Reference-Cited by-同舟云学术

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Chemoselective Divergent Transformations of N-(Propargyl)indole-2-carbonitriles with Nitrogen Nucleophiles: Alkyne Hydroamination or Domino Cyclizations

Published:2022-10-03 Issue:21 Volume:87 Page:13663-13671
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Zalte Rajesh R.¹,Festa Alexey A.¹^ORCID,Raspertov Pavel V.¹,Storozhenko Olga A.¹,Golantsov Nikita E.¹^ORCID,Rybakov Victor B.²,Varlamov Alexey V.¹,Voskressensky Leonid G.¹^ORCID

Affiliation:

1. Organic Chemistry Department, Science Faculty, Peoples’ Friendship University of Russia (RUDN University), Miklukho-Maklaya st., 6, Moscow 117198, Russia

2. Department of Chemistry, Lomonosov Moscow State University, Leninskie Gory, 1-3, Moscow 119991, Russia

Funder

Russian Foundation for Basic Research

RUDN University

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c01327

Reference25 articles.

1. Indoles as therapeutics of interest in medicinal chemistry: Bird's eye view

2. Indoles — A promising scaffold for drug development

3. Synthesis of indoles: recent advances

4. Synthesis of pyrazino[1,2-a]indoles and indolo-[1,2-a]quinoxalines (microreview)

5. Synthesis and Biological Activities of Pyrazino[1,2-a]indole and Pyrazino[1,2-a]indol-1-one Derivatives

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1. The chemistry of heterocycles in the 21st century;Russian Chemical Reviews;2024-07

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