Copper-Catalyzed Regioselective [4 + 1 + 1] Annulation to 1,2-Oxazines Using Dioxazolones and H <sub>2</sub> O as the Heteroatom Sources

O) to build molecular complexity. This method features mild conditions, exclusive regioselectivity, and broad functional group compatibility, offering a modular alternative to traditional nitroso Diels-Alder (NDA) chemistry.

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Publication Details

Journal
Organic Letters
Published
2026-05-11
DOI
https://doi.org/10.1021/acs.orglett.6c01526
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Copper-Catalyzed Regioselective [4 + 1 + 1] Annulation to 1,2-Oxazines Using Dioxazolones and H 2 O as the Heteroatom Sources

Lu Xu, Liuxin Luo, Tiankui Huang, Yu Wei et al.
Organic Letters
Catalytic C–H Functionalization Methods
article

Copper-Catalyzed Regioselective [4 + 1 + 1] Annulation to 1,2-Oxazines Using Dioxazolones and H 2 O as the Heteroatom Sources

Lu Xu, Liuxin Luo, Tiankui Huang, Yu Wei, Shuai Liu, Liang Xu, Huanhuan Song
article en

Abstract

O) to build molecular complexity. This method features mild conditions, exclusive regioselectivity, and broad functional group compatibility, offering a modular alternative to traditional nitroso Diels-Alder (NDA) chemistry.

Organic Letters
Shihezi University (CN), Silicon Chemical (United States) (US)
Shihezi University
Openalex Percentile: Top 10%
Catalytic C–H Functionalization Methods
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Copper-Catalyzed Regioselective [4 + 1 + 1] Annulation to 1,2-Oxazines Using Dioxazolones and H <sub>2</sub> O as the Heteroatom Sources — Lu Xu, Liuxin Luo, et al. · Organic Letters (2026) | TGRS Research Map | TGRS