Artigas Albert, Vila Jordi, Lledó Agustí, Solà Miquel, Pla-Quintana Anna, Roglans Anna
Institut de Química Computacional i Catàlisi (IQCC) and Departament de Química, Universitat de Girona (UdG), Facultat de Ciències, C/Maria Aurèlia Capmany, 69, 17003-Girona, Catalunya, Spain.
Org Lett. 2019 Sep 6;21(17):6608-6613. doi: 10.1021/acs.orglett.9b02032. Epub 2019 Jul 11.
A novel methodology to transform bisallenes into a variety of polycyclic derivatives employing rhodium(I) catalysis has been developed. This transformation encompasses an intramolecular Rh-catalyzed cycloisomerization of bisallenes to deliver a reactive cycloheptadiene, which concomitantly undergoes a regioselective [4 + 2] cycloaddition with alkenes. A complete mechanistic study of this transformation has been undertaken including DFT calculations. Overall, the methodology presented here constitutes a new and straightforward entry to polycyclic dihydroazepine and dihydrooxepine derivatives employing catalytic methods.
已经开发出一种利用铑(I)催化将双烯丙基转化为多种多环衍生物的新方法。这种转化包括双烯丙基的分子内铑催化环异构化,以生成一种反应性环庚二烯,该环庚二烯随后与烯烃进行区域选择性的[4 + 2]环加成反应。已经对这种转化进行了完整的机理研究,包括密度泛函理论(DFT)计算。总体而言,本文介绍的方法构成了一种采用催化方法合成多环二氢氮杂卓和二氢氧杂卓衍生物的新颖且直接的途径。