Laboratoire de Chimie Organique, Service de Chimie et PhysicoChimie Organiques, Université Libre de Bruxelles (ULB) , Avenue F. D. Roosevelt 50, CP160/06, 1050 Brussels, Belgium.
J Am Chem Soc. 2014 Sep 10;136(36):12528-31. doi: 10.1021/ja504818p. Epub 2014 Jun 30.
A novel and efficient keteniminium-initiated cationic polycyclization is reported. This reaction, which only requires triflic acid or bistriflimide as promoters, affords a straightforward entry to polycyclic nitrogen heterocycles possessing up to three contiguous stereocenters and seven fused cycles. These complex, polycyclic molecules can be obtained in a single operation from readily available ynamides which were shown to be remarkable building blocks for multiple, consecutive cationic transformations.
报告了一种新颖高效的偕二酮亚胺引发的阳离子多环化反应。该反应仅需三氟磺酸或双三氟甲磺酰亚胺作为促进剂,可直接得到具有多达三个连续立体中心和七个稠合环的多环氮杂环化合物。这些复杂的多环分子可以通过易得的炔酰胺一步合成得到,炔酰胺被证明是多种连续阳离子转化的优异构建块。