| Literature DB >> 34061546 |
Xin Jin1, Hong-Chen Fu2, Mei-Yan Wang1,3,4, Shouying Huang1, Yue Wang1, Liang-Nian He4,2, Xinbin Ma1,3,4.
Abstract
The development of selective catalytic reactions that utilize easily available reagents for the efficient synthesis of alcohols is a long-standing goal of chemical research. Here an intriguing strategy for the chemodivergent copper-catalyzed hydroxymethylation of alkynes with formic acid and hydrosilane has been developed. By simply tuning the amount of formic acid and reaction temperature, distinct one-carbon-extended primary alcohols, that is, allylic alcohols and β-branched alkyl alcohols, were produced with high levels of Z/E-, regio-, and enantioselectivity.Entities:
Year: 2021 PMID: 34061546 DOI: 10.1021/acs.orglett.1c01473
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005