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.
Authors
- Yukie Ide
- Yoshihiko Yamamoto (ORCID: https://orcid.org/0000-0001-8544-6324)
- Takeshi Yasui (ORCID: https://orcid.org/0000-0002-7630-8736)
Institutions
- Nagoya University (JP)
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
Funders
- Japan Agency for Medical Research and Development