Transmission of Molecular Structure on NMR Characteristics of Phosphorus-Nitrogen Double Bond Systems

1999 ◽  
Vol 147 (1) ◽  
pp. 103-103
Author(s):  
Dietrich Gudat ◽  
Edgar Niecke ◽  
Gisbert Grossmann ◽  
Kerstin Krüger
1962 ◽  
Vol 3 (26) ◽  
pp. 1269-1274 ◽  
Author(s):  
D.Y. Curtin ◽  
C.G. McCarty

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.


1945 ◽  
Vol 18 (2) ◽  
pp. 280-283
Author(s):  
G. A. Jeffrey

Abstract The x-ray diffraction data at present available from β-gutta-percha are shown to be insufficient to distinguish fine details of molecular structure. Since a qualitative estimate of the intensities on the fibre diagram can be adequately satisfied by a model having normal interatomic distances and valency angles, no evidence exists for the improbable distortion of the methyl group out of the plane of the double bond previously ascribed to the molecule.


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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