Palladium-Catalyzed [2+3] Cycloaddition/Cross-Coupling Reaction: Z/E and Diastereoselective Synthesis of Dendralene-Functionalized Dihydrofurans
Xiangyu Tan, Qianqian Gu, Xingjiang Yang, Yingying Yang, Bingwei Hu, Shuai Mao, Jun Lin*, and Yi Jin*
Organic Letters 2022, 24, 24, 4383–4388
Publication Date: June 13, 2022
DOI：https://doi.org/10.1021/acs.orglett.2c01605
Abstract
Herein, we describe a Pd-catalyzed [2+3] cycloaddition/cross-coupling reaction of allenyl acetates for the Z/E selective and diastereoselective synthesis of dendralene-functionalized dihydrofurans. Remarkably, mechanistic studies show the formation of an epoxide from a carbonyl bond via cycloaddition, which is practically and mechanistically significant for the construction of other bioactive heterocyclic epoxides. This research also revealed the utility and potential of allenic esters as C2 synthons and 1,2-biselectrophiles in cycloaddition reactions.
