1452849-46-5Relevant academic research and scientific papers
Synthesis of the aziridinomitosene skeleton by application of guanidinium ylide-mediated aziridination
Kojima, Hiroyuki,Takahata, Chisato,Lemin, David,Takahashi, Masato,Kumamoto, Takuya,Nakanishi, Waka,Suzuki, Noriyuki,Ishikawa, Tsutomu
, p. 379 - 388 (2013)
An aziridinomitosene skeleton, a basic core of mitomycin antibiotics, was straightforwardly prepared from N-(p-toluenesulfonyl)indole-2-carboxaldehyde in 16% overall yield by successive reactions of guanidinium ylide-mediated aziridination, InCl3-catalyzed epimerization of trans-3-(indol-2-yl) aziridine-2-carboxylate, leading to the cis-derivative, and dehydrative cyclization. Copyright
