Lewis酸催化施-受体斯坦豪斯加合物的4π-电环化

IF 2.2 4区化学 Q2 CHEMISTRY, ORGANIC

Synthesis-Stuttgart Pub Date : 2023-09-27 DOI:10.1055/a-2182-9098

Seung Hyeon Yoon, Kye Sung Park, Jaehee Kim, Yonghoon Kwon

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引用次数: 0

摘要

摘要研究了Lewis酸催化施-受体斯坦豪斯加合物(DASAs)的4π电环化反应。利用Dy(OTf)3的催化量，实现了无环dasa向相应的环化异构体的高效转化。值得注意的是，这种转变表现出了非凡的产量，特别是在第一代dasa的情况下。此外，Lewis酸催化使“供体”和“受体”组分一锅合成环戊酮产物成为可能。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

Lewis Acid Catalyzed 4π-Electrocyclization of Donor-Acceptor Stenhouse Adducts

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Lewis Acid Catalyzed 4π-Electrocyclization of Donor-Acceptor Stenhouse Adducts

Abstract Lewis acid catalyzed 4π-electrocyclization of Donor–Acceptor Stenhouse Adducts (DASAs) has been developed. By employing catalytic quantities of Dy(OTf)3, a highly efficient transformation of acyclic DASAs into the corresponding cyclized isomers was achieved. Notably, this transformation exhibited exceptional yields, particularly in the case of first generation DASAs. In addition, Lewis acid catalysis enabled one-pot synthesis of the cyclopentenone product from the ‘donor’ and ‘acceptor’ components.

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来源期刊

Synthesis-Stuttgart 化学-有机化学

CiteScore

4.50

自引率

7.70%

发文量

435

审稿时长

1 months

期刊介绍： SYNTHESIS is an international full-paper journal devoted to the advancement of the science of chemical synthesis. It covers all fields of organic chemistry involving synthesis, including catalysis, organometallic, medicinal, biological, and photochemistry, but also related disciplines. SYNTHESIS provides dependable research results with detailed and reliable experimental procedures and full characterization of all important new products as well as scientific primary data.