Nitrene Transfer‐Triggered Novel <i>Oxa</i> −Pictet−Spengler Reaction: A Versatile Approach to Amino‐Functionalized Dihydropyran Scaffolds

= 2.2) reveal that C-H bond cleavage is involved in the rate-determining step. This work provides a versatile strategy for accessing amino-dihydropyran scaffolds, merging nitrene transfer with the oxa-Pictet-Spengler reaction for the first time.

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Publication Details

Journal
Chemistry - A European Journal
Published
2026-04-11
DOI
https://doi.org/10.1002/chem.70977
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Nitrene Transfer‐Triggered Novel Oxa −Pictet−Spengler Reaction: A Versatile Approach to Amino‐Functionalized Dihydropyran Scaffolds

Yi Yang, Lijia Wang, Xu Liu, Teng Sun
Chemistry - A European Journal
Catalytic C–H Functionalization Methods
article

Nitrene Transfer‐Triggered Novel Oxa −Pictet−Spengler Reaction: A Versatile Approach to Amino‐Functionalized Dihydropyran Scaffolds

Yi Yang, Lijia Wang, Xu Liu, Teng Sun
article en

Abstract

= 2.2) reveal that C-H bond cleavage is involved in the rate-determining step. This work provides a versatile strategy for accessing amino-dihydropyran scaffolds, merging nitrene transfer with the oxa-Pictet-Spengler reaction for the first time.

Chemistry - A European Journal
East China Normal University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 21%
Catalytic C–H Functionalization Methods
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