1196977-45-3Relevant academic research and scientific papers
Synthetic Studies on Cyclocitrinol: Construction of the ABC Ring System Based on Epoxy-Nitrile Cyclization
Sato, Kazuto,Tanino, Keiji
, p. 674 - 678 (2021/01/21)
The stereoselective synthesis of a model compound containing the ABC ring system of cyclocitrinol was accomplished. After connecting a C ring allyltitanium segment with an A ring bi? cyclo[4.1.0]heptanone segment, the seven-membered B ring moiety was cons
A raney-cobalt-mediated tandem reductive cyclization route to the 1,5-methanoazocino[4,3-b]indole framework of the uleine and strychnos alkaloids
Reekie, Tristan A.,Banwell, Martin G.,Willis, Anthony C.
, p. 10773 - 10781 (2013/02/22)
The readily accessible enones 8, 17, and 18 undergo 2-fold reductive cyclization reactions upon exposure to hydrogen in the presence of Raney-cobalt and thereby afford compounds 11 (72%), 19 (47%), and 20 (84%), respectively. These products embody the ABC
Expedient synthesis of 3-substituted cycloalkanones via a Pd-catalyzed decarboxylative protonation protocol
Kim, Se Hee,Kim, Eun Sun,Kim, Taek Hyeon,Kim, Jae Nyoung
experimental part, p. 6256 - 6260 (2010/01/11)
We developed an efficient method for the introduction of -CH2EWG moiety at the β-position of 2-cycloalken-1-ones via a Pd-catalyzed decarboxylative protonation protocol.
