@article{oai:kutarr.kochi-tech.ac.jp:00000301,
 author = {Asahara, Haruyasu and Muto, Kyo and Nishiwaki, Nagatoshi},
 issue = {37},
 journal = {Tetrahedron},
 month = {Sep},
 note = {A practical, convenient, and safe cyano(nitro)methylation method was developed, in which cyano-aci-nitroacetate served as a synthetic equivalent of anionic nitroacetonitrile. A control of the single/double Michael additions was achieved, which enabled the synthesis of unsymmetrical double Michael adducts. Moreover, the Michael adducts can be used as precursors of pyridine and naphthyridine frameworks.},
 pages = {6522--6528},
 title = {Safe cyano(nitro)methylating reagent—Michael addition of cyano-aci-nitroacetate leading to δ-functionalized α-nitronitriles},
 volume = {70},
 year = {2014}
}