Instituto Universitario de Bio-Orgánica Antonio González (CIBICAN), Departamento de Química Orgánica, Universidad de La Laguna , Avda. Astrofísico Francisco Sánchez No. 2, 38206, La Laguna, Tenerife, Spain.
Instituto de Biotecnología-Instituto de Ciencias Básicas, Universidad Nacional de San Juan , Av. Libertador General San Martín 1109 (O), CP 5400, San Juan, Argentina.
J Org Chem. 2016 Oct 21;81(20):9738-9756. doi: 10.1021/acs.joc.6b01818. Epub 2016 Oct 6.
A highly efficient and regioselective approach to new polycyclic embelin derivatives through a domino Knoevenagel condensation/intramolecular hetero Diels-Alder reaction using O-(arylpropynyloxy)-salicylaldehydes in the presence of ethylenediamine diacetate (EDDA) is reported. This organocatalyzed protocol is compatible toward a wide range of aryl-substituted alkynyl ethers with electron-donating and electron-withdrawing groups. When other active methylene compounds were subjected to this domino reaction the corresponding adducts were obtained in high yield.
本文报道了一种通过邻苯二酚缩甲醛与芳香炔基醚的 Knoevenagel 缩合/分子内杂 Diels-Alder 反应高效构建新型多环 embelin 衍生物的方法。该方法在乙二胺二乙酸酯(EDDA)存在下使用 O-(芳基丙炔氧基)水杨醛作为多组分反应的底物,具有广泛的官能团容忍性。当其他活性亚甲基化合物作为亲偶极体参与该多组分反应时,也能以高产率得到相应的加合物。