1. Atroposelective Construction of Tetrasubstituted Axially Chiral Alkene Frameworks.
- Author
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Zou, Jia-Yu, Xu, Wan-Yi, Wang, Jie, Liu, Qi, and He, Ying
- Subjects
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ALKENES , *RING formation (Chemistry) , *KINETIC resolution , *KINETIC control , *ARYL iodides , *CHIRALITY element , *COUPLING reactions (Chemistry) , *CHEMICAL properties , *INDOLE derivatives - Abstract
This document provides a summary of various methods for the synthesis of tetrasubstituted axially chiral alkenes. The methods discussed include urea group-directed organocatalytic dihalogenation, Rh(III)-catalyzed C-H activation and directing group migration, cationic rhodium(I)/H8-BINAP-catalyzed chelation-controlled cycloaddition, Cu/Pd dual catalysis for arylboration, nickel-catalyzed cross-electrophile trans-aryl-benzylation, palladium-catalyzed C-H functionalization, Pd(II)-catalyzed thioether-directed alkenyl C-H olefination, Suzuki-Miyaura cross-coupling, asymmetric N-alkylation, chiral phosphoric acid catalyzed kinetic resolution, and asymmetric allylic substitution-isomerization. The methods demonstrate broad substrate scope and high enantioselectivities, but further research is needed to explore stereodivergent synthesis and applications in pharmaceutical chemistry. [Extracted from the article]
- Published
- 2024
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