Transition metal-catalyzed alkynylation reactions via alkynyl carbon-carbon bond cleavage

被引:4
|
作者
Yuan, Hairui [1 ]
Zhou, Qi [1 ]
Wang, Jianbo [1 ,2 ]
机构
[1] Peking Univ, Coll Chem, Beijing Natl Lab Mol Sci BNLMS, Key Lab Bioorgan Chem & Mol Engn,Minist Educ, Beijing 100871, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
关键词
ASYMMETRIC CONJUGATE ALKYNYLATION; ONE-POT SYNTHESIS; H-PHOSPHINE OXIDES; N-TOSYLHYDRAZONES; C-C; SONOGASHIRA REACTION; SELECTIVE SYNTHESIS; PROPARGYL ALCOHOLS; COUPLING REACTIONS; FACILE SYNTHESIS;
D O I
10.1039/d3qo00225j
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
It is of great significance to realize the alkynylation of the reaction since alkynes are widely present in natural products and biologically active molecules. And at the same time alkynes have very rich transformations in synthetic organic chemistry. It is also attractive to functionalize molecules by cleaving inert carbon-carbon bonds albeit with great challenge due to their inherent stability. Recently, significant progress has been made in the cleavage of alkynyl carbon-carbon single bonds for enabling the alkynylation of organic molecules. This review focuses on the recent advances in transition-metal-catalyzed cleavage and transformation of alkynyl carbon-carbon bonds with alkynoic acids, propargylic alcohols, alkynyl esters, and alkynyl ketones.
引用
收藏
页码:2081 / 2094
页数:14
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