958246-89-4Relevant academic research and scientific papers
Internal azomethine ylide cycloaddition methodology for access to the substitution pattern of aziridinomitosene A
Bobeck, Drew R.,Warner, Don L.,Vedejs, Edwin
, p. 8506 - 8518 (2007)
(Chemical Equation Presented) Highly substituted, tethered alkyne dipolarophiles participate in the internal 2 + 3 cycloaddition with azomethine ylides generated by treatment of oxazolium salts with cyanide ion. Starting from oxazole 26, a sequence of N-m
