TY - JOUR
T1 - Catalytic coupling of terminal alkynes with isonitriles promoted by organoactinide complexes
AU - Barnea, Eyal
AU - Andrea, Tamer
AU - Kapon, Moshe
AU - Berthet, Jean Claude
AU - Ephritikhine, Michel
AU - Eisen, Moris S.
PY - 2004/9/8
Y1 - 2004/9/8
N2 - The coupling reaction of terminal alkynes and tert-butylisonitrile to yield substituted α,β-acetylenic aldimines is catalyzed by the organoactinide neutral complexes Cp*2AnMe2 (Cp* = C5Me5, An = Th, U) and the cationic complex [(Et2N)3U][BPh4]. The reaction proceeds by a 1,1-insertion of the isonitrile into the metal-acetylide bond. Additional insertion products can be obtained by altering the catalyst and the reactant ratios. A plausible mechanism for the catalytic reaction is presented, in addition to the crystal structure of Cp*2UMe2.
AB - The coupling reaction of terminal alkynes and tert-butylisonitrile to yield substituted α,β-acetylenic aldimines is catalyzed by the organoactinide neutral complexes Cp*2AnMe2 (Cp* = C5Me5, An = Th, U) and the cationic complex [(Et2N)3U][BPh4]. The reaction proceeds by a 1,1-insertion of the isonitrile into the metal-acetylide bond. Additional insertion products can be obtained by altering the catalyst and the reactant ratios. A plausible mechanism for the catalytic reaction is presented, in addition to the crystal structure of Cp*2UMe2.
UR - http://www.scopus.com/inward/record.url?scp=4444271324&partnerID=8YFLogxK
U2 - 10.1021/ja046604a
DO - 10.1021/ja046604a
M3 - 文章
C2 - 15339168
AN - SCOPUS:4444271324
SN - 0002-7863
VL - 126
SP - 10860
EP - 10861
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 35
ER -