1042424-75-8Relevant academic research and scientific papers
Consecutive cyclization of allylaminoalkene by intramolecular aminolithiation-carbolithiation
Tsuchida, Susumu,Kaneshige, Atsunori,Ogata, Tokutaro,Baba, Hiromi,Yamamoto, Yasutomo,Tomioka, Kiyoshi
supporting information; experimental part, p. 3635 - 3638 (2009/05/07)
(Chemical Equation Presented) Consecutive cyclization of allylaminoalkenes by tandem aminolithiation-carbolithiation proceeded smoothly by using a lithium amide as a lithiating agent as well as protonating agent to give bicyclic amines, octahydroindolizine and hexahydro-1H-pyrrollzine, in reasonably high yield and diastereoselectivity.
