Gharpure Santosh J, Prasath V, Shelke Yogesh G
Department of Chemistry , Indian Institute of Technology Bombay , Powai, Mumbai 400076 , India.
Org Lett. 2019 Jan 4;21(1):223-227. doi: 10.1021/acs.orglett.8b03668. Epub 2018 Dec 24.
A single alkynyl vinylogous carbonate was elaborated to tetrasubstituted furan or dihydrofuran via a cascade inter-intramolecular radical reaction by changing the radical being added. The strategy could be used in the synthesis of polycyclic heterocycles as well as bis-furan exhibiting atropisomerism. Installation of a new furan motif on the existing one was feasible by iteration. Stannyl dihydrofuran derivative was used in Stille coupling, whereas intramolecular Friedel-Crafts acylation on the furan gave furanonaphthol.
通过改变所添加的自由基,单一的炔基烯醇碳酸酯可通过级联分子间-分子内自由基反应转化为四取代呋喃或二氢呋喃。该策略可用于多环杂环以及具有阻转异构现象的双呋喃的合成。通过迭代在现有的呋喃基序上引入新的呋喃基序是可行的。甲锡烷基二氢呋喃衍生物用于施蒂勒偶联反应,而呋喃上的分子内傅克酰基化反应则生成呋喃并萘酚。