Mandal Pratap Kumar, Katukojvala Sreenivas
Department of Chemistry, Indian Institute of Science Education & Research, Bhopal, Madhya Pradesh, 462066.
Chemistry. 2024 Apr 2;30(19):e202303862. doi: 10.1002/chem.202303862. Epub 2024 Jan 22.
Novel rhodium-catalyzed [3+3] annulations of diazoenals and α-amino ketones has been disclosed here. The reactivity of diazoenals has been switched from carbenoid to vinylogous NH-insertion by altering acyclic to cyclic α-amino ketones. In this direction, we report an efficient strategy to synthesize 1,2-dihydropyridines (DHPs) and fused 1,4-oxazines. Mechanistic investigation revealed that the formyl group is necessary for carbenoid [3+3] annulation and the cyclohexyl group is the dictating factor for vinylogous NH- insertion. The synthetic utility of 1,2-dihydropyridines was demonstrated by synthesizing piperidine, pyrido[1,2-a]indole, and 2-pyridone scaffolds. Further, structural diversification of fused 1,4-oxazines resulted in the short synthesis of hexahydroquinolin-2(1H)-ones, hexahydro quinolines and tetrahydroquinolinones via ring opening rearrangement and a new oxidative deformylation, respectively.
本文报道了一种新型铑催化的重氮烯醛与α-氨基酮的[3+3]环化反应。通过将无环α-氨基酮改为环状α-氨基酮,重氮烯醛的反应活性从类卡宾反应转变为烯丙基NH插入反应。在此方向上,我们报道了一种合成1,2-二氢吡啶(DHP)和稠合1,4-恶嗪的有效策略。机理研究表明,甲酰基对于类卡宾[3+3]环化反应是必需的,而环己基是烯丙基NH插入反应的决定性因素。通过合成哌啶、吡啶并[1,2-a]吲哚和2-吡啶酮骨架展示了1,2-二氢吡啶的合成效用。此外,稠合1,4-恶嗪的结构多样化分别通过开环重排和一种新的氧化脱甲酰基反应,实现了六氢喹啉-2(1H)-酮、六氢喹啉和四氢喹啉酮的简短合成。