Organocatalytic Enantioselective Synthesis of Atropisomeric Aryl-p-Quinones: Platform Molecules for Diversity-Oriented Synthesis of Biaryldiols

被引:83
作者
Chen, Ye-Hui [1 ,2 ]
Li, Heng-Hui [1 ,2 ]
Zhang, Xiao [1 ,2 ]
Xiang, Shao-Hua [1 ,2 ,3 ]
Li, Shaoyu [1 ,2 ,3 ]
Tan, Bin [1 ,2 ]
机构
[1] Southern Univ Sci & Technol, Guangdong Prov Key Lab Catalysis, Shenzhen Grubbs Inst, Shenzhen 518055, Peoples R China
[2] Southern Univ Sci & Technol, Guangdong Prov Key Lab Catalysis, Dept Chem, Shenzhen 518055, Peoples R China
[3] Southern Univ Sci & Technol, Acad Adv Interdisciplinary Studies, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
atropisomerism; biaryls; chirality; organocatalysis; quinones; FRIEDEL-CRAFTS ALKYLATION; ATROPOSELECTIVE SYNTHESIS; 2-NAPHTHOL DERIVATIVES; AXIAL CHIRALITY; ASYMMETRIC-SYNTHESIS; OXIDATIVE COUPLINGS; PHOSPHORIC-ACID; ALPHA-ARYLATION; BRONSTED ACID; BINOL;
D O I
10.1002/anie.202004671
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Presented here is a class of novel axially chiral aryl-p-quinones as platform molecules for the preparation of non-C-2 symmetric biaryldiols. Two sets of aryl-p-quinone frameworks were synthesized with remarkable enantiocontrol by means of chiral phosphoric acid catalyzed enantioselective arylation of p-quinones by central-to-axial chirality conversion. These aryl-p-quinones were then used to access a wide spectrum of highly functionalized non-C-2 symmetric biaryldiols with excellent retention of the enantiopurity.
引用
收藏
页码:11374 / 11378
页数:5
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