118355-85-4Relevant articles and documents
Tandem 1,3-Dipolar Cycloadditions of Pyridinium or Isoquinolinium Methylides with Olefinic Dipolarophiles Leading to Cyclazines. "Enamine Route" as a New Generation Method of Azomethine Ylides
Kanemasa, Shuji,Takenaka, Shigeori,Watanabe, Haruyuki,Tsuge, Otohiko
, p. 420 - 424 (2007/10/02)
Pyridinium or isoquinolinium methylides undergo tandem 1,3-dipolar cycloadditions with two molecules of olefins to produce cyclazine derivatives in a highly regioselective, stereoselective, and face-selective manner.A new generation of azomethine y