Journal
CHEMICAL COMMUNICATIONS
Volume 52, Issue 11, Pages 2257-2260Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5cc08880a
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Funding
- Shanghai Pujiang Program [14PJ1403100]
- 973 programs [2015CB856600]
- National Natural Science Foundation of China [21572065, 21425205, 21372084]
- Shanghai Eastern Scholar Program
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Herein, a novel and efficient gold-catalyzed intermolecular C(sp(2))-H functionalization (Friedel-Crafts alkylation) and aldol annulation strategy is presented. This cascade process allows the synthesis of a series of indanol and tetrahydronaphthalenol derivatives with two adjacent quaternary stereocenters. The attractive reaction features are the use of readily available starting materials, good diastereo-selectivity, good functional-group tolerance and mild reaction conditions. Furthermore, preliminary results indicate that this transformation is amenable to enantioselectivitive synthesis with further chiral ligand screening and design.
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