1-Bromalkynes as π-nucleophiles in acyliminium ion cyclilizations. a formal synthesis of lupinine and epilupinine.
作者:J.P. Gesson、J.C. Jacquesy、D. Rambaud
DOI:10.1016/s0040-4039(00)92521-8
日期:1992.6
The use of a 1-bromoalkyne as pi-nucleophile in the alpha-N-acyliminium ion cyclization of a glutarimide derivative results in the formation of a single bromoenol triflate 11 in triflic acid-trifluoroacetic and of a mixture (E/Z: 4/1) of bromofluoro derivatives 12a,b in HF, 11 is quantitatively converted to esters 9a,b which are also obtained after trifluoroscetic acid treatment and methanolysis. 9a,b are known precursors of lupinine and epilupinine.