Two-Step Synthesis of 1,3-Oxazin-6-One Derivatives Involving <i>N-</i> Selective Alkenylation of Isoxazol-5-Ones Using β-Phenylsulfonylenone Alkenyl Donors
A highly regioselective <i>N</i>-alkenylation of isoxazol-5-ones using β-phenylsulfonylenones as alkenyl donors quickly afforded <i>N</i>-alkenylisoxazol-5-one derivatives in excellent yield. Subsequent treatment of these derivatives with 1,8-diazabicyclo(5.4.0)undec-7-ene (DBU) generated 1,3-oxazin-6-one derivatives in high yield. To our knowledge, this report is the first report to successfully synthesize 1,3-oxazin-5-one derivatives via <i>N</i>-selective alkenylation of isoxazol-5-one derivatives and subsequent transformation of the resulting <i>N</i>-alkenylisoxazol-5-ones.
Authors
- Yuta Iino
- Kosuke Nakashima (ORCID: https://orcid.org/0000-0001-9323-3521)
- Tsuyoshi Miura (ORCID: https://orcid.org/0000-0003-1216-4507)
- Shin‐ichi Hirashima (ORCID: https://orcid.org/0000-0001-8125-5010)
- Yasuyuki Matsushima
Institutions
- Tokyo University of Pharmacy and Life Sciences (JP)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2025-11-05
- DOI
- https://doi.org/10.1021/acs.joc.5c02517
- Citations
- 2
- Primary Topic
- Cyclopropane Reaction Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 1.87