Selective COSY-J -resolved-HMBC, a new method for improving sensitivity of cross peaks of methine proton signals attached to a methyl group

2012 ◽  
Vol 50 (6) ◽  
pp. 409-414 ◽  
Author(s):  
Kazuo Furihata ◽  
Mitsuru Tashiro
1969 ◽  
Vol 10 (7) ◽  
pp. 561-564 ◽  
Author(s):  
James J. Sims ◽  
L.H. Selman

2010 ◽  
Vol 51 (30) ◽  
pp. 3960-3961 ◽  
Author(s):  
Isao Kadota ◽  
Takayuki Kishi ◽  
Yuka Fujisawa ◽  
Yuji Yamagami ◽  
Hiroyoshi Takamura

Tetrahedron ◽  
1970 ◽  
Vol 26 (22) ◽  
pp. 5191-5194 ◽  
Author(s):  
J.F.W. Keana ◽  
R.R. Schumaker

ChemInform ◽  
2010 ◽  
Vol 41 (46) ◽  
pp. no-no
Author(s):  
Isao Kadota ◽  
Takayuki Kishi ◽  
Yuka Fujisawa ◽  
Yuji Yamagami ◽  
Hiroyoshi Takamura

1994 ◽  
Vol 72 (5) ◽  
pp. 1225-1229
Author(s):  
Fernande D. Rochon ◽  
Guylaine Laperrière

Complexes of the type [Pt(L)X] where L is a tridentate N ligand and X = Cl or I, were synthesized and characterized. Three of the ligands are N-derivatives of diethylenetriamine, (2-aminoethyl)(N-dimethyl-2-aminoethyl)amine, (2-aminoethyl)(N-diethyl-2-aminoethyl)amine, and (2-aminoethyl)(N-methyl-2-aminoethyl)N-methylamine. The other two ligands are di(3-amino-propyl)amine and (2-aminoethyl)(3-aminopropyl)amine. A new method for the synthesis of the chloro complexes from the direct reaction of the amine with K2[PtCl4] was developed. The reactions of these five compounds with several purine and pyrimidine bases were studied by NMR techniques. The Pt(II) complexes containing two five-membered chelates were shown to be more reactive than the one containing two six-membered rings, while the complex containing one five- and one six-membered chelates showed intermediate reactivity. For the diethylenetriamine derivatives, the complexes containing ligands with two alkyl groups on the same terminal N atom were more reactive than the one containing one methyl group on a terminal N atom and one methyl group on a non-terminal N atom.


Author(s):  
C. C. Clawson ◽  
L. W. Anderson ◽  
R. A. Good

Investigations which require electron microscope examination of a few specific areas of non-homogeneous tissues make random sampling of small blocks an inefficient and unrewarding procedure. Therefore, several investigators have devised methods which allow obtaining sample blocks for electron microscopy from region of tissue previously identified by light microscopy of present here techniques which make possible: 1) sampling tissue for electron microscopy from selected areas previously identified by light microscopy of relatively large pieces of tissue; 2) dehydration and embedding large numbers of individually identified blocks while keeping each one separate; 3) a new method of maintaining specific orientation of blocks during embedding; 4) special light microscopic staining or fluorescent procedures and electron microscopy on immediately adjacent small areas of tissue.


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