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

Institutions

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
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Two-Step Synthesis of 1,3-Oxazin-6-One Derivatives Involving N- Selective Alkenylation of Isoxazol-5-Ones Using β-Phenylsulfonylenone Alkenyl Donors

Yuta Iino, Kosuke Nakashima, Tsuyoshi Miura, Shin‐ichi Hirashima et al.
2 citations
The Journal of Organic Chemistry
Cyclopropane Reaction Mechanisms
1.87
article

Two-Step Synthesis of 1,3-Oxazin-6-One Derivatives Involving N- Selective Alkenylation of Isoxazol-5-Ones Using β-Phenylsulfonylenone Alkenyl Donors

Yuta Iino, Kosuke Nakashima, Tsuyoshi Miura, Shin‐ichi Hirashima, Yasuyuki Matsushima
article en
2 citations

Abstract

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.

The Journal of Organic ChemistryVol. 90(45)
Tokyo University of Pharmacy and Life Sciences (JP)
Openalex Percentile: Top 13%
Cyclopropane Reaction Mechanisms
1.87
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.