1446-76-0Relevant academic research and scientific papers
Access to Benzylic Quaternary Carbons from Aromatic Ketones
Li, You,Han, Jingpeng,Luo, Han,An, Qiaoyu,Cao, Xiao-Ping,Li, Baosheng
, p. 6050 - 6053 (2019)
The construction of benzylic all-carbon quaternary stereocenters, which are ubiquitous in biomolecules and drugs, is a task of high practical significance. Herein, we disclose a highly efficient one-pot method of constructing all-carbon quaternary structu
β-Bromoenol phosphate as a new precursor for the modular regioselective synthesis of substituted furans
Fernandes, Rushil,Mhaske, Krishna,Narayan, Rishikesh
supporting information, (2021/11/24)
Owing to its importance in various realms of chemistry, furan occupies a position of eminence among heterocycles. Despite the availability of many methodologies for the synthesis of variably substituted furans, a modular convenient synthesis of 2,4-disubstituted furans remains challenging. The present work attempts to bridge that gap through a novel annulation-based approach using feedstock chemicals such as methyl ketones and their easily available derivatives, β-bromoenol phosphates. We have demonstrated a hitherto unknown reactivity of β-bromoenol phosphates which is responsible for the observed regioselectivity. The reaction requires only sodium hydride as the base under mild conditions. The scope of the reaction was found to be broad with the possibility of obtaining even tri-substituted furans besides a variety of 2,4-disubstituted furans. The methodology was applied to obtain synthetically challenging 3-acylfuran derivatives as well. The newly developed methodology is characterized by the modularity, regioselectivity as well as its practicality owing to easily available starting materials and fast reaction times.
