Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Stephen D. Wobser"'
Publikováno v:
Organometallics. 32:1317-1327
Facile carbon–tin bond activation in the reaction of 2-(trimethylstannyl)pyridine (1) with the organolanthanide complexes Cp*2LaCH(TMS)2 (2a) and [Cp*2LaH]2 (2b) yields Cp*2La(2-pyridyl) (3), as well as Me3SnCH(TMS)2 and Me3SnH, respectively. At ro
Autor:
Stephen D. Wobser, Tobin J. Marks
Publikováno v:
Organometallics. 32:2517-2528
Organothorium complexes bearing amide or alkyl proligands are active toward the highly selective hydroalkoxylation/cyclization of alkynyl alcohols. Substrates include primary and secondary alcohols, as well as terminal and internal alkynes. Catalysts
Publikováno v:
Organometallics. 29:6308-6320
The Markovnikov-selective lanthanide- and actinide-mediated, intermolecular hydrothiolation of terminal alkynes by aliphatic, benzylic and aromatic thiols using Cp*2LnCH(TMS)2 (Cp* = C5Me5; Ln = La, Sm, Lu), Ln[N(TMS)2]3 (Ln = La, Nd, Y), Cp*2An(CH2T
Publikováno v:
Journal of Organometallic Chemistry. 692:5331-5338
The reaction of 2,6-(2-{Me2NCH2}C6H4)2C6H3I (2) with Pd2(dba)3 produced the NCN diamine pincer complex [2,6-(2-Me2{NCH2}C6H4)2C6H3PdI] (3) by an oxidative addition route. The structural analysis of ligand precursor 2 revealed a syn-conformation in th
Publikováno v:
ChemInform. 40
Atom-efficient organoactinide-catalyzed intermolecular hydrothiolation of terminal alkynes is achieved by Th(IV) and U(IV) complexes to yield vinyl sulfides. The conversion is highly Markovnikov selective and is capable of utilizing aromatic, benzyli
Publikováno v:
Journal of the American Chemical Society. 131:2062-2063
Atom-efficient organoactinide-catalyzed intermolecular hydrothiolation of terminal alkynes is achieved by Th(IV) and U(IV) complexes to yield vinyl sulfides. The conversion is highly Markovnikov selective and is capable of utilizing aromatic, benzyli
Publikováno v:
Organometallics; Dec2010, Vol. 29 Issue 23, p6308-6320, 13p