scholarly journals Intramolecular Transfer of Pd Catalyst on Carbon–Carbon Triple Bond and Nitrogen–Nitrogen Double Bond in Suzuki–Miyaura Coupling Reaction

Catalysts ◽  
2017 ◽  
Vol 7 (7) ◽  
pp. 195 ◽  
Author(s):  
Takeru Kamigawara ◽  
Hajime Sugita ◽  
Koichiro Mikami ◽  
Yoshihiro Ohta ◽  
Tsutomu Yokozawa
1962 ◽  
Vol 3 (26) ◽  
pp. 1269-1274 ◽  
Author(s):  
D.Y. Curtin ◽  
C.G. McCarty

ChemInform ◽  
2008 ◽  
Vol 39 (24) ◽  
Author(s):  
Huili Qiu ◽  
Shaheen M. Sarkar ◽  
Dong-Hwan Lee ◽  
Myung-Jong Jin

1990 ◽  
Vol 112 (19) ◽  
pp. 6803-6809 ◽  
Author(s):  
James C. Duchamp ◽  
Marek Pakulski ◽  
Alan H. Cowley ◽  
Kurt W. Zilm

1987 ◽  
Vol 40 (10) ◽  
pp. 1777 ◽  
Author(s):  
AF Hegarty ◽  
P Rigopoulos ◽  
JE Rowe

Rate data for the reaction of a series of benzohydrazonoyl halides with pyrrolidine and butan- 1-amine at 303 K are presented. Linear Hammett plots were obtained with each amine. The mechanism of the reactions and the stereochemical outcome of these displacements at the carbon-nitrogen double bond are discussed.


2012 ◽  
Vol 68 (6) ◽  
pp. o1812-o1812 ◽  
Author(s):  
Ioannis Tiritiris ◽  
Willi Kantlehner

The reaction of 3,3,3-tris(dimethylamino)-1-phenylprop-1-yne with bromine in pentane yields the title compound, C13H17N2 +·Br−. The acetylenic bond distance [1.197 (2) Å] is consistent with a C[triple-bond]C triple bond. The amidinium C=N bonds [1.325 (2) and 1.330 (2) Å] have double-bond character and the positive charge is delocalized between the two dimethylamino groups.


1963 ◽  
Vol 41 (11) ◽  
pp. 2836-2838 ◽  
Author(s):  
M. H. Benn

A new synthesis of mustard oil glucosides is described, illustrated by the synthesis of glucotropaeolin. This synthesis, based on the reaction of thiols with nitrile oxides, leads to a conclusion concerning the stereochemistry about the carbon–nitrogen double bond in the mustard oil glucosides.


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