Photoinduced Functionalization of <i>p‐/o</i> ‐Quinone Methides

Abstract Quinone methides (QMs) are highly reactive intermediates and important building blocks for diverse molecular scaffolds. In recent years, there has been remarkable growth in the area of quinone methide photochemistry. Under photoirradiation conditions, p ‐quinone methides ( p ‐QMs) exhibit versatile chemical reactivity as electrophilic acceptors for radical addition and annulation reactions. However, o ‐quinone methides ( o ‐QMs) are mostly involved in photocyclization reactions. This review sheds light on recent advancements (2020–mid 2025) in photoinduced functionalization of p‐/o ‐quinone methides to form diverse molecular scaffolds, especially emphasizing their mechanistic insights.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2025-07-14
DOI
https://doi.org/10.1002/ajoc.202500516
Citations
2
Primary Topic
Synthesis of Indole Derivatives
Type
article
Field-Weighted Citation Impact
1.87
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article

Photoinduced Functionalization of p‐/o ‐Quinone Methides

Suven Das
2 citations
Asian Journal of Organic Chemistry
Synthesis of Indole Derivatives
1.87
article

Photoinduced Functionalization of p‐/o ‐Quinone Methides

Suven Das
article en
2 citations

Abstract

Abstract Quinone methides (QMs) are highly reactive intermediates and important building blocks for diverse molecular scaffolds. In recent years, there has been remarkable growth in the area of quinone methide photochemistry. Under photoirradiation conditions, p ‐quinone methides ( p ‐QMs) exhibit versatile chemical reactivity as electrophilic acceptors for radical addition and annulation reactions. However, o ‐quinone methides ( o ‐QMs) are mostly involved in photocyclization reactions. This review sheds light on recent advancements (2020–mid 2025) in photoinduced functionalization of p‐/o ‐quinone methides to form diverse molecular scaffolds, especially emphasizing their mechanistic insights.

Asian Journal of Organic ChemistryVol. 14(9)
Reserve Bank of India (IN)
Openalex Percentile: Top 15%
Synthesis of Indole Derivatives
1.87
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