53872-19-8Relevant articles and documents
Nickel(II)-catalyzed diastereoselective [3+2] cycloaddition of N-tosyl-aziridines and aldehydes via selective carbon-carbon bond cleavage
Wu, Xingxing,Li, Lei,Zhang, Junliang
, p. 7824 - 7826 (2011)
An efficient and mild Ni(ClO4)2-catalyzed [3+2] cycloaddition of N-tosylaziridines and aldehydes via C-C bond cleavage was developed. The cycloaddition reaction proceeds with high diastereoselectivity and regioselectivity leading to
RhII-catalyzed cycloadditions of carbomethoxy iodonium ylides
Batsila, Christina,Kostakis, George,Hadjiarapoglou, Lazaros P
, p. 5997 - 6000 (2007/10/03)
Carbomethoxy iodonium ylides, generated from methyl acetoacetate and methyl malonate, respectively, are exploited in synthesis of cyclopropanes, cyclopropenes as well as various heterocycles.
Rhodium-catalyzed heterocycloaddition route to 1,3-oxazoles as building blocks in natural products synthesis
Connell,Tebbe,Gangloff,Helquist,Akermark
, p. 5445 - 5459 (2007/10/02)
Rhodium(II) acetate serves as a catalyst for the heterocycloaddition reaction of diazodicarbonyl compounds with nitriles to give functionalized 1,3-oxazole derivatives in a simple one-step procedure. In particular, dimethyl diazomalonate undergoes this re