Palladium-Catalyzed Hydroformylation of Alkenes and Alkynes

被引:17
作者
Zhang, Yang [1 ]
Sigrist, Michel [1 ]
Dydio, Pawel [1 ]
机构
[1] Univ Strasbourg, CNRS, UMR 7006, ISIS, 8 Allee Gaspard Monge, F-67000 Strasbourg, France
基金
欧洲研究理事会;
关键词
Aldehydes; Alkenes; Alkynes; Hydroformylation; Pd-catalysis; ZWITTERIONIC RHODIUM COMPLEX; REGIOSELECTIVE HYDROFORMYLATION; SUPRAMOLECULAR CONTROL; ALPHA; BETA-UNSATURATED ALDEHYDES; ASYMMETRIC HYDROFORMYLATION; SELECTIVE HYDROFORMYLATION; BRANCHED ALDEHYDES; OLEFINS; LIGAND; EFFICIENT;
D O I
10.1002/ejoc.202101020
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Hydroformylation of alkenes and alkynes with syngas represents a method of choice to furnish valuable aldehydes with the 100 % atom-economy from readily available building blocks. The field is dominated by Rh- and Co-catalysis; however, complexes of many other metals were also shown to be catalytically competent. Here we review the studies of hydroformylation under Pd-catalysis, starting from the seminal reports up to the most recent examples. Special emphasis is paid to the unique regio- and chemoselectivities of Pd-based methods, which are difficult to achieve with the conventional hydroformylation protocols. Different mechanistic proposals are presented along with a summary of their experimental and computational support. Finally, the user-friendly methods using surrogates of syngas are discussed as well. Overall, the Minireview aims to present unique opportunities and remaining challenges of Pd-catalyzed hydroformylation reactions for their prospective applications in fine-chemical synthesis.
引用
收藏
页码:5985 / 5997
页数:13
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