KANG, HY HONG, WS CHO, YS KOH, HY 2024-01-21T20:33:09Z 2024-01-21T20:33:09Z 2022-01-11 1995-10 0040-4039 https://pubs.kist.re.kr/handle/201004/144955 Decyanation of geminal dinitriles and alpha-alkoxycarbonyl substituted nitriles promoted by samarium(II) iodide has been efficiently achieved. This method has advantages over the previously known radical route using tin hydride with respect to applicable substrates and the reaction temperature employed. This decyanation could broaden the synthetic applicability of the nitrile derivatives. English Elsevier BV Reductive decyanation of α-cyano and α-alkoxycarbonyl substituted nitriles promoted by samarium(II) iodide Article 10.1016/0040-4039(95)01606-I 1 Tetrahedron Letters, v.36, no.42, pp.7661 - 7664 Tetrahedron Letters 36 42 7661 7664 N scie scopus A1995RZ29500023 2-s2.0-0028862802 Chemistry, Organic Chemistry Article ORGANIC-SYNTHESIS LANTHANIDES