Dearomative Transformation of Pyridin-3-ols into 2,3,6,7-Tetrahydro-1<i>H</i>-2,6-methanobenzo[<i>d</i>]azonin-12-ones via Oxidopyridinium/<i>o</i>-Quinodimethane (5 + 4) Cycloaddition

We report the dearomative transformation of pyridin-3-ols via oxidopyridinium (5 + 4) cycloaddition with <i>o</i>-quinodimethanes, leading to 2,3,6,7-tetrahydro-1<i>H</i>-2,6-methanobenzo[<i>d</i>]azonin-12-ones. The chemoselective derivatization of the obtained cycloadduct was also investigated to demonstrate the synthetic potential of the obtained cycloadduct.

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Publication Details

Journal
Organic Letters
Published
2024-12-23
DOI
https://doi.org/10.1021/acs.orglett.4c03878
Citations
1
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
0.25

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article

Dearomative Transformation of Pyridin-3-ols into 2,3,6,7-Tetrahydro-1H-2,6-methanobenzo[d]azonin-12-ones via Oxidopyridinium/o-Quinodimethane (5 + 4) Cycloaddition

Yukie Ide, Yoshihiko Yamamoto, Takeshi Yasui
1 citations
Organic Letters
Oxidative Organic Chemistry Reactions
0.25
article

Dearomative Transformation of Pyridin-3-ols into 2,3,6,7-Tetrahydro-1H-2,6-methanobenzo[d]azonin-12-ones via Oxidopyridinium/o-Quinodimethane (5 + 4) Cycloaddition

Yukie Ide, Yoshihiko Yamamoto, Takeshi Yasui
article en
1 citations

Abstract

We report the dearomative transformation of pyridin-3-ols via oxidopyridinium (5 + 4) cycloaddition with <i>o</i>-quinodimethanes, leading to 2,3,6,7-tetrahydro-1<i>H</i>-2,6-methanobenzo[<i>d</i>]azonin-12-ones. The chemoselective derivatization of the obtained cycloadduct was also investigated to demonstrate the synthetic potential of the obtained cycloadduct.

Organic LettersVol. 27(1)
Nagoya University (JP)
Japan Agency for Medical Research and Development
Clean water and sanitation
Openalex Percentile: Top 45%
Oxidative Organic Chemistry Reactions
0.25
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