A unified strategy to access N-heterocycles enabled by hypervalent iodine( <scp>iii</scp> ) reagent-mediated imidate radical cyclization

A hypervalent iodine( iii ) reagent-assisted imidate radical cyclization strategy for the synthesis of diverse N -heterocycles has been developed.

Authors

Akshay S. Pathare
Sermadurai Selvakumar

Institutions

Indian Institute of Management Indore (IN)
Indian Institute of Technology Indore (IN)

Publication Details

Journal: Organic Chemistry Frontiers
Published: 2026-01-01
DOI: https://doi.org/10.1039/d5qo01301a
Primary Topic: Oxidative Organic Chemistry Reactions
Type: article
Field-Weighted Citation Impact: 0.00

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article

A unified strategy to access N-heterocycles enabled by hypervalent iodine( iii ) reagent-mediated imidate radical cyclization

Akshay S. Pathare, Sermadurai Selvakumar

Jan 1, 2026

Organic Chemistry Frontiers

Oxidative Organic Chemistry Reactions

article

A unified strategy to access N-heterocycles enabled by hypervalent iodine( iii ) reagent-mediated imidate radical cyclization

Akshay S. Pathare, Sermadurai Selvakumar

January 1, 2026article en

Abstract

A hypervalent iodine( iii ) reagent-assisted imidate radical cyclization strategy for the synthesis of diverse N -heterocycles has been developed.

Organic Chemistry FrontiersVol. 13(6)

Indian Institute of Management Indore (IN), Indian Institute of Technology Indore (IN)

Openalex Percentile: Top 96%

Oxidative Organic Chemistry Reactions

DOI Source OpenAlex

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A unified strategy to access N-heterocycles enabled by hypervalent iodine( <scp>iii</scp> ) reagent-mediated imidate radical cyclization — Akshay S. Pathare, Sermadurai Selvakumar · Organic Chemistry Frontiers (2026) | TGRS Research Map | TGRS