Unveiling catalyst-free electro-photochemical reactivity of aryl diazoesters and facile synthesis of oxazoles, imide-fused pyrroles and tetrahydro-epoxy-pyridines <i>via</i> carbene radical anions-Reference-Cited by-同舟云学术

Unveiling catalyst-free electro-photochemical reactivity of aryl diazoesters and facile synthesis of oxazoles, imide-fused pyrroles and tetrahydro-epoxy-pyridines via carbene radical anions

Published:2023 Issue:23 Volume:14 Page:6216-6225
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Maiti Debajit¹^ORCID,Saha Argha²,Guin Srimanta²,Maiti Debabrata²^ORCID,Sen Subhabrata¹^ORCID

Affiliation:

1. Department of Chemistry, School of Natural Sciences, Shiv Nadar Institution of Eminence Deemed to be University, Chithera, Dadri, Gautam Buddha Nagar, UP 201314, India

2. Department of Chemistry, IIT-Bombay, Powai, Mumbai 400076, MH, India

Abstract

First ever catalyst-free electro-photochemical generation of carbene radical anion from aryl diazoester with direct application into synthesis of interesting N-heterocycles with broad substrate scope and excellent diastereo-selectivity.

Funder

Shiv Nadar University

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/SC/D3SC00089C

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1. Powering the Future: How Can Electrochemistry Make a Difference in Organic Synthesis?

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3. Synthetic Organic Electrochemistry: An Enabling and Innately Sustainable Method