Gogoi Abhijit, Chouhan Raju, Das Sajal Kumar
Department of Chemical Sciences, Tezpur University, Napaam, Sonitpur-784028, Assam, India.
Org Lett. 2025 Mar 14;27(10):2461-2466. doi: 10.1021/acs.orglett.5c00420. Epub 2025 Mar 3.
Described herein is a mild catalytic dehydrative Friedel-Crafts alkylation of 1,1-diarylalkanols─a challenging reaction with exceedingly rare previous success, presumably because of the unfavorable steric hindrance around the reactive centers and the competitive E1 reaction. Executing in an intramolecular fashion and benefiting from the high nucleophilicity of indole, we have successfully utilized this reaction in synthesizing 3,4-fused indoles. Interestingly, the Friedel-Crafts alkylation strategy could also be applied to access 4,5-fused indoles via modification of the tether connecting the alcohol and indole moieties.
本文描述了一种温和的催化脱水傅克烷基化反应,用于1,1-二芳基烷醇的反应——这是一个具有挑战性的反应,此前成功的案例极为罕见,推测是由于反应中心周围不利的空间位阻和竞争性的E1反应。以分子内方式进行反应,并受益于吲哚的高亲核性,我们成功地利用该反应合成了3,4-稠合吲哚。有趣的是,通过修饰连接醇和吲哚部分的连接链,傅克烷基化策略也可用于合成4,5-稠合吲哚。