Institut für Organische und Biomolekulare Chemie, Georg-August-Universität Göttingen, Tammannstr. 2, 37077 Göttingen, Germany.
Bioorg Med Chem. 2010 Jun 1;18(11):3656-67. doi: 10.1016/j.bmc.2010.03.004. Epub 2010 Mar 10.
Herein we describe the synthesis of highly substituted chromans and isochromans using carbohydrates as starting materials. The key step of our synthetic approach is the annelation of the benzene moiety via a highly efficient Pd-catalyzed domino reaction. This powerful approach led to a small library of highly substituted chromans and isochromans by making use of a variety of different diynes and bromoglycals. We investigated several Pd-catalysts in order to improve the yields and to enlarge the scope of the domino reaction. Furthermore, we elucidated the mechanistic picture of the reaction with isotope-labelling experiments. Most probably the reaction proceeds via an oxidative addition followed by two carbopalladation steps and a final cyclization reaction.
在这里,我们描述了使用碳水化合物作为起始原料合成高度取代的色满和异色满。我们合成方法的关键步骤是通过高效的钯催化的多米诺反应将苯环部分环合。通过利用各种不同的二炔和溴代糖苷,这种强大的方法得到了一个包含多种高度取代的色满和异色满的小文库。我们研究了几种钯催化剂,以提高产率并扩大多米诺反应的范围。此外,我们还通过同位素标记实验阐明了反应的机理。该反应很可能通过氧化加成,接着是两个碳钯化步骤和最终的环化反应进行。