Recent advances in the generation and functionalization of C(alkenyl)-Pd species for synthesis of polysubstituted alkenes

被引:13
|
作者
Liu, Mingyu [1 ]
Sun, Juntao [1 ]
Engle, Keary M. [1 ]
机构
[1] Scripps Res Inst, Dept Chem, 10550 N Torrey Pines Rd, La Jolla, CA 92037 USA
基金
美国国家科学基金会;
关键词
Palladium; Alkene; Cross-coupling; C-H activation; Regioselectivity; C-H BOND; PALLADIUM-CATALYZED HYDROARYLATION; ORGANOBORONIC ACIDS; STEREOSELECTIVE-SYNTHESIS; OLEFINATION REACTION; NEGISHI COUPLINGS; SUZUKI-MIYAURA; ALKYNES; CYCLIZATION; CARBOCYCLIZATION;
D O I
10.1016/j.tet.2021.132513
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The synthesis of polysubstituted alkenes represents a formidable challenge in organic synthesis. Over the years, many advances have been made for this purpose, yet challenges persist in terms of selectivity, scope, and efficiency. Palladium-catalyzed methods for alkene synthesis are attractive within this field given that cross-coupling is particularly impactful in the construction of organic molecules due to palladium's ability to facilitate modular carbon-carbon and carbon-heteroatom bond formation. To employ palladium catalysis for alkene synthesis, the generation and subsequent functionalization of C(alkenyl)-Pd intermediates are key steps. In this review, we highlight research advances since 2000 in the area of polysubstituted alkene syntheses involving C(alkenyl)-Pd species. (c) 2021 Elsevier Ltd. All rights reserved.
引用
收藏
页数:16
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