| Literature DB >> 32003369 |
Xiong-Fei Deng1, Ying-Wei Wang, Shi-Qi Zhang, Ling Li, Guang-Xun Li, Gang Zhao, Zhuo Tang.
Abstract
Hydroxyl alkylation of indoles by Friedel-Crafts reaction with a carbonyl compound is a useful strategy. However, the reaction was restricted to ketones due to the easy formation of a bisindole byproduct. Therefore, hydroxyl alkylation of an aldehyde with indole is confronted with great challenges. Here, we report an efficient strategy for asymmetric hydroxyl alkylation of 2-substituted indoles with aldehydes under 0.1 mol% chiral phosphoric acid. A series of α-hydroxyl ketones were obtained in high yields (up to 99%) and good enantioselectivities (up to 97%).Entities:
Year: 2020 PMID: 32003369 DOI: 10.1039/c9cc09637j
Source DB: PubMed Journal: Chem Commun (Camb) ISSN: 1359-7345 Impact factor: 6.222