Palladium‐Catalyzed Oxidative Alkynylation of Allenyl Ketones: Access to 3‐Alkynyl Poly‐substituted Furans

Author:

Dou Bowen1,Wang Kang1,Wang Jianbo12

Affiliation:

1. Beijing National Laboratory of Molecular Sciences (BNLMS) and Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry Peking University Beijing 100871 China

2. The State Key Laboratory of Organometallic Chemistry Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences 354 Fenglin Lu Shanghai 200032 China

Abstract

Comprehensive SummaryFurans bearing alkynyl substituents are highly useful in organic synthesis. However, the methodologies to access these important furan derivatives are rather limited. We herein report an efficient synthesis of alkynylated furan derivatives based on Pd‐catalyzed oxidative cross‐coupling reaction between allenyl ketones and terminal alkynes. This novel synthesis of alkynylated furans with wide substrate scope is operationally simple and tolerates various functional groups. Mechanistically, the formation of the palladium carbene through cycloisomerization and the subsequent alkynyl migratory insertion are proposed as the key steps in the transformation. The reaction reported in this paper further demonstrates the generality of the carbene‐based cross coupling.

Publisher

Wiley

Subject

General Chemistry

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