Synthesis of functionalized furo[3,2-c]coumarins via a one-pot oxidative pseudo three-component reaction in poly(ethylene glycol)
摘要:
An efficient and straightforward synthesis of functionalized furo[3,2-c]coumarins via a one-pot oxidative pseudo three-component condensation of aldehydes and 4-hydroxycoumarin (2 equiv) in poly(ethylene glycol) (PEG) as solvent is described. A mixture of I-2 and K2S2O8 in the presence of Na2CO3 was used as an oxidative reagent. The structure of the furo[3,2-c]coumarins was established by X-ray single crystal structure analysis. (c) 2012 Elsevier Ltd. All rights reserved.
DMSO and iodine mediated reaction of 4-hydroxycoumarins and aldehydes/aryl methyl ketones: synthesis of furo[3,2-c]coumarins
作者:Sinki Kolita、Pallabi Borah、P. Seetham Naidu、Pulak J. Bhuyan
DOI:10.1016/j.tet.2015.12.016
日期:2016.1
and efficient method for the synthesis of highly functionalized furo[3,2-c]coumarins was developed. The reaction occurred via initial formation of biscoumarins from the reaction of 4-hydroxycoumarins and aldehydes/aryl methyl ketones in the presence of molecular iodine in DMSO followed by lactone ring opening, cyclization and oxidative aromatization process. The reaction conditions were moderate, work-up
开发了一种简单高效的合成高度官能化的呋喃[3,2- c ]香豆素的方法。该反应是在DMSO中存在分子碘的情况下,由4-羟基香豆素与醛/芳基甲基酮的反应最初生成双香豆素而发生的,然后是内酯开环,环化和氧化芳构化过程。反应条件温和,后处理步骤简单,并且以高收率获得产物。
Copper(<scp>ii</scp>) bromide-catalyzed intramolecular decarboxylative functionalization to form a C(sp<sup>3</sup>)–O bond for the synthesis of furo[3,2-c]coumarins
作者:W. L. Zhang、S. N. Yue、Y. M. Shen、H. Y. Hu、Q.-H. Meng、H. Wu、Y. Liu
DOI:10.1039/c4ob02490g
日期:——
Copper(ii) bromide-catalyzed intramolecular decarboxylative functionalization to form a C(sp3)–O bond has been developed.