Scholay

学术搜索 · AI 审稿 · LaTeX 协作

Photochemical and Thermal Ring-Contraction of Cyclic Hydroxamic Acid Derivatives

作者:Simon Pichette, Samuel Aubert‐Nicol, Jean Lessard, Claude Spino · 发表于:The Journal of Organic Chemistry · 年份:2012 · DOI:10.1021/jo3023507 · 被引用次数:22 · 研究领域:Asymmetric Synthesis and Catalysis、Synthesis and Catalytic Reactions、Synthetic Organic Chemistry Methods

Cyclic hydroxamic acids can undergo a thermal ring contraction after an in situ triflation. High yields of ring-contraction products are obtained with DBU when the migrating carbon is a methylene, while best results are obtained with Et(3)N for the migration of quaternary carbons. In some cases, the regiochemical outcome of the reaction can be controlled by changing the base. This novel thermal rearrangement complements a similar but photochemical rearrangement of N-mesyloxylactams.