Ligand-controlled regiodivergent -allyl palladium catalysis enables a switch between [3+2] and [3+3] cycloadditions

被引:34
|
作者
Xia, Yu [1 ]
Bao, Qiao-Fei [1 ]
Li, Yuke [2 ,3 ]
Wang, Li-Jing [4 ]
Zhang, Bo-Sheng [1 ]
Liu, Hong-Chao [1 ]
Liang, Yong-Min [1 ]
机构
[1] Lanzhou Univ, Sch Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Gansu, Peoples R China
[2] Chinese Univ Hong Kong, Dept Chem, Shatin, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Ctr Sci Modeling & Computat, Shatin, Hong Kong, Peoples R China
[4] HeBei Univ, Coll Chem & Environm Sci, Key Lab Med Chem & Mol Diag, Minist Educ, 180 Wusi Donglu, Baoding 071002, Peoples R China
基金
中国国家自然科学基金;
关键词
VINYLETHYLENE CARBONATES; DECARBOXYLATIVE CYCLOADDITION; ENANTIOSELECTIVE SYNTHESIS; NUCLEOPHILIC-ATTACK; REGIOSELECTIVE SYNTHESIS; PROPARGYLIC ALCOHOLS; CONSTRUCTION; BOND; REARRANGEMENT; HETEROCYCLES;
D O I
10.1039/c9cc00611g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Reported herein is the use of ligands to tune the regioselectivity and reactivity of palladium-catalyzed [3+2] and [3+3] cycloadditions. Diverse synthesis with vinylethylene carbonates (VECs) as well as free naphthols has been explored to construct four different valuable polycyclic frameworks in a broad substrate scope.
引用
收藏
页码:4675 / 4678
页数:4
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