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Organocatalytic Enantioselective Synthesis of Atropisomeric Aryl-p-Quinones: Platform Molecules for Diversity-Oriented Synthesis of Biaryldiols.
Chen, Ye-Hui; Li, Heng-Hui; Zhang, Xiao; Xiang, Shao-Hua; Li, Shaoyu; Tan, Bin.
Affiliation
  • Chen YH; Shenzhen Grubbs Institute and Department of Chemistry, Guangdong Provincial Key Laboratory of Catalysis, Southern University of Science and Technology, Shenzhen, 518055, China.
  • Li HH; Shenzhen Grubbs Institute and Department of Chemistry, Guangdong Provincial Key Laboratory of Catalysis, Southern University of Science and Technology, Shenzhen, 518055, China.
  • Zhang X; Shenzhen Grubbs Institute and Department of Chemistry, Guangdong Provincial Key Laboratory of Catalysis, Southern University of Science and Technology, Shenzhen, 518055, China.
  • Xiang SH; Shenzhen Grubbs Institute and Department of Chemistry, Guangdong Provincial Key Laboratory of Catalysis, Southern University of Science and Technology, Shenzhen, 518055, China.
  • Li S; Academy for Advanced Interdisciplinary Studies, Southern University of Science and Technology, Shenzhen, 518055, China.
  • Tan B; Shenzhen Grubbs Institute and Department of Chemistry, Guangdong Provincial Key Laboratory of Catalysis, Southern University of Science and Technology, Shenzhen, 518055, China.
Angew Chem Int Ed Engl ; 59(28): 11374-11378, 2020 07 06.
Article in En | MEDLINE | ID: mdl-32277551
Presented here is a class of novel axially chiral aryl-p-quinones as platform molecules for the preparation of non-C2 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-C2 symmetric biaryldiols with excellent retention of the enantiopurity.
Key words

Full text: 1 Database: MEDLINE Language: En Journal: Angew Chem Int Ed Engl Year: 2020 Type: Article Affiliation country: China

Full text: 1 Database: MEDLINE Language: En Journal: Angew Chem Int Ed Engl Year: 2020 Type: Article Affiliation country: China