Dehydrocoupling Reactions of Secondary and Primary Amine–Borane Adducts Catalyzed by Half-sandwich Carbonyl Complexes, [CpMn(CO)3], [(η6-C6H6)Cr(CO)3], and [CpV(CO)4]

2011 ◽  
Vol 40 (2) ◽  
pp. 171-173 ◽  
Author(s):  
Taeko Kakizawa ◽  
Yasuro Kawano ◽  
Kohsuke Naganeyama ◽  
Mamoru Shimoi
Polyhedron ◽  
1988 ◽  
Vol 7 (19-20) ◽  
pp. 2027-2030 ◽  
Author(s):  
W.A. Herrmann ◽  
W.R. Thiel ◽  
E. Herdtweck

2002 ◽  
Vol 664 (1-2) ◽  
pp. 214-222 ◽  
Author(s):  
Anne-Cécile Hervé ◽  
Jean-Jacques Yaouanc ◽  
Jean-Claude Clément ◽  
Hervé des Abbayes ◽  
Loı̈c Toupet

2009 ◽  
Vol 131 (41) ◽  
pp. 14946-14957 ◽  
Author(s):  
Yasuro Kawano ◽  
Mikio Uruichi ◽  
Mamoru Shimoi ◽  
Seitaro Taki ◽  
Takayuki Kawaguchi ◽  
...  

ACS Catalysis ◽  
2017 ◽  
Vol 7 (10) ◽  
pp. 6827-6842 ◽  
Author(s):  
Kai Y. Wan ◽  
Molly M. H. Sung ◽  
Alan J. Lough ◽  
Robert H. Morris

1986 ◽  
Vol 47 (C8) ◽  
pp. C8-589-C8-592
Author(s):  
N. BINSTED ◽  
S. L. COOK ◽  
J. EVANS ◽  
R. J. PRICE ◽  
G. N. GREAVES

2020 ◽  
Author(s):  
Rémi Blieck ◽  
Sebastien Lemouzy ◽  
Marc Taillefer ◽  
Florian Monnier

A dual copper/enamine catalytic system is found to enable an intermolecular enantioselective α-addition of various carbonyl nucleophiles to allenamides. Secondary amine catalysts allowed the highly enantioselective addition of aldehydes, while using primary amine catalysts led to the enantioselective addition of ketoester nucleophiles. The process was found to be highly regio-, stereo- and enantio-selective and represented the first allene hydrofunctionalization using an synergistic catalysis involving copper


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