Institut für Chemie, Universität Rostock, Albert Einstein Str. 3a, 18059, Rostock, Germany.
Org Biomol Chem. 2011 Jul 21;9(14):5172-84. doi: 10.1039/c1ob05455d. Epub 2011 Jun 3.
Bis-cyclopropanated 1,3,5-tricarbonyl compounds were prepared by a sequence of Claisen condensations and cyclopropanations. The optimization of the conditions proved to be very important to suppress retro-Claisen reactions. The conformation of these molecules was studied by experimental and computational methods. The syn/syn;syn/syn conformation is present for all derivatives. It is exclusively present in the case of the derivative containing a phenyl group located at the terminal carbon atom. In most cases, equilibria with other conformers are found.
双环丙基 1,3,5-三羰基化合物是通过一系列克莱森缩合和环丙烷化反应制备的。条件的优化被证明对抑制逆克莱森反应非常重要。通过实验和计算方法研究了这些分子的构象。所有衍生物均呈现 syn/syn;syn/syn 构象。仅当末端碳原子上含有苯基的衍生物存在这种构象。在大多数情况下,都会发现与其他构象的平衡。