Base-Mediated Direct Transformation of N-Propargylamines into 2,3,5-Trisubstituted 1H-Pyrroles-Reference-Cited by-同舟云学术

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Base-Mediated Direct Transformation of N-Propargylamines into 2,3,5-Trisubstituted 1H-Pyrroles

Published:2018-11-08 Issue:22 Volume:20 Page:7182-7185
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Mishra Pawan K.¹,Verma Shalini¹,Kumar Manoj¹,Verma Akhilesh K.¹^ORCID

Affiliation:

1. Department of Chemistry, University of Delhi, Delhi 110007, India

Funder

University of Delhi

Council of Scientific and Industrial Research

University Grants Commission

Science and Engineering Research Board

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.8b03112

Reference57 articles.

1. Biological formation of pyrroles: Nature's logic and enzymatic machinery

2. Identification of (1H)-pyrroles as histone deacetylase inhibitors with antitumoral activity

3. Lamellarins and Related Pyrrole-Derived Alkaloids from Marine Organisms

4. Living on pyrrolic foundations – Advances in natural and artificial bioactive pyrrole derivatives

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3. Facile synthesis of propargylamines by metal-free doubly decarboxylative coupling;RSC Sustainability;2024

4. Base‐Promoted Synthesis of N−H Free Pyrroles via net [3+2]‐Cycloaddition;Advanced Synthesis & Catalysis;2023-11-13

5. Base-Promoted [4 + 2] Annulation Reaction of In Situ-Generated Azadienes from N-Propargylamines with Active Methylene Compounds: Access to Highly Functionalized 2-Pyridones;The Journal of Organic Chemistry;2023-10-19

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