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Mikl s Nyerges Monika Rudas G bor T th Bulcsú Her nyi Istv n K das Istv n Bitter L szl T ke 《Tetrahedron》1995,51(48):13321-13330
The 1,3-dipolar cycloadditions of ester stabilised azomethin ylides to aryl-nitro olefines catalysed by Li(I) gave products of different stereoselectivity than those arising from processes catalysed by Ag (I). The cycloadditions involve the stereospecific generation of dipoles. The formation of products with reverse stereochemistry when using different metal salt catalysts is caused by the differences in endo and exo approaches of nitro-ethylene compounds. 相似文献
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Inside Back Cover: RuII,OsII, and IrIII Complexes with Chelating Pyridyl–Mesoionic Carbene Ligands: Structural Characterization and Applications in Transfer Hydrogenation Catalysis (Chem. Eur. J. 18/2015) 
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Gustav F. Hüttig und Margarethe Kantor 《Fresenius' Journal of Analytical Chemistry》1931,86(1-4):95-98
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