Structure and reactivity in intramolecular catalysis. Catalysis of sulfonamide hydrolysis by the neighboring carboxyl group

1979 ◽  
Vol 101 (23) ◽  
pp. 6981-6991 ◽  
Author(s):  
Teun Graafland ◽  
Anno Wagenaar ◽  
Anthony J. Kirby ◽  
Jan B. F. N. Engberts
Keyword(s):  
Carboxyl Group ◽  
Intramolecular Catalysis

Intramolecular catalysis of sulfonamide hydrolysis by a neighbouring carboxyl group

1974 ◽  
Vol 15 (43) ◽  
pp. 3735-3738 ◽  
Author(s):  
A. Wagenaar ◽  
A.J. Kirby ◽  
Jan B.F.N. Engberts
Keyword(s):  
Carboxyl Group ◽  
Intramolecular Catalysis

ChemInform Abstract: STRUCTURE AND REACTIVITY IN INTRAMOLECULAR CATALYSIS. CATALYSIS OF SULFONAMIDE HYDROLYSIS BY THE NEIGHBORING CARBOXYL GROUP

1980 ◽  
Vol 11 (7) ◽  
Author(s):  
T. GRAAFLAND ◽  
A. WAGENAAR ◽  
A. J. KIRBY ◽  
J. B. F. N. ENGBERTS
Keyword(s):  
Carboxyl Group ◽  
Intramolecular Catalysis ◽  
Abstract Structure

Additions and Corrections - Structure and Reactivity in Intramolecular Catalysis. Catalysis of Sulfonamide Hydrolysis by the Neighboring Carboxyl Group

1980 ◽  
Vol 102 (10) ◽  
pp. 3663-3663
Author(s):  
Teun Graafland ◽  
Anno Wagenaar ◽  
Anthony Kirby ◽  
Jan Engberts
Keyword(s):  
Carboxyl Group ◽  
Intramolecular Catalysis

ChemInform Abstract: INTRAMOLECULAR CATALYSIS OF SULFONAMIDE HYDROLYSIS BY A NEIGHBOURING CARBOXYL GROUP

1975 ◽  
Vol 6 (3) ◽  
pp. no-no
Author(s):  
A. WAGENAAR ◽  
A. J. KIRBY ◽  
J. B. F. N. ENGBERTS
Keyword(s):  
Carboxyl Group ◽  
Intramolecular Catalysis

Structural Study of a new Compound Based on Acid 1,4-Cyclohexanedicarboxylic (1,4-CDC)

2010 ◽  
Vol 6 (1) ◽  
pp. 891-896
Author(s):  
Manel Halouani ◽  
M. Dammak ◽  
N. Audebrand ◽  
L. Ktari
Keyword(s):  
Aqueous Solution ◽  
Water Molecules ◽  
Carboxyl Group ◽  
X Ray Diffraction ◽  
Compound I ◽  
Unit Cell Parameters ◽  
Monoclinic System ◽  
X Ray ◽  
Cell Parameters ◽  
Cyclohexanedicarboxylic Acid

One nickel 1,4-cyclohexanedicarboxylate coordination polymers, Ni2 [(O10C6H4)(COO)2].2H2O  (I), was hydrothermally synthesized from an aqueous solution of Ni (NO3)2.6H2O, (1,4-CDC) (1,4-CDC = 1,4-cyclohexanedicarboxylic acid) and tetramethylammonium nitrate. Compound (I) crystallizes in the monoclinic system with the C2/m space group. The unit cell parameters are a = 20.1160 (16) Å, b = 9.9387 (10) Å, c = 6.3672 (6) Å, β = 97.007 (3) (°), V= 1263.5 (2) (Å3) and Dx= 1.751g/cm3. The refinement converged into R= 0.036 and RW = 0.092. The structure, determined by single crystal X-ray diffraction, consists of two nickel atoms Ni (1) and Ni (2). Lots of ways of which is surrounded by six oxygen atoms, a carboxyl group and two water molecules.

Preparation and Performance of Crosslinked Proton Exchange Membranes Containing Carboxyl Group

2012 ◽  
Vol 29 (12) ◽  
pp. 1428
Author(s):  
Hong WEI ◽  
Hong JIANG ◽  
Lei NI
Keyword(s):  
Proton Exchange Membranes ◽  
Proton Exchange ◽  
Carboxyl Group ◽  
And Performance

17O, 13C, and 29Si NMR spectra of some acyloxy- and diacetoxysilanes and acetoxygermanes

1986 ◽  
Vol 51 (11) ◽  
pp. 2582-2589 ◽  
Author(s):  
Antonín Lyčka ◽  
Jaroslav Holeček ◽  
Karel Handlíř ◽  
Josef Pola ◽  
Václav Chvalovský
Keyword(s):  
Periodic System ◽  
Time Scale ◽  
Nmr Spectra ◽  
Group Element ◽  
29Si Nmr ◽  
Carboxyl Group ◽  
29Si Nmr Spectra ◽  
Oxygen Atoms

The 17O, 13C, and 29Si NMR spectra of (CH3)3SiOC(O)R, CH3(XCH2)Si(OC(O)CH3)2, and R3GeOC(O)CH3 compounds are reported. In the 17O NMR spectra at 350 K the only signal is observed with the two latter series, but two well-resolved signals are displayed with the (CH3)3SiOC(O)R compounds. The equivalence of both oxygen atoms in carboxyl group on the NMR time scale is discussed from the viewpoint of a possible coordination of the oxygen atoms to the IVB group element of the periodic system.

Some 2-substitution derivatives of 5-(4-oxo-6-hydroxy-3,4-dihydro-5-pyrimidinyl)pentanoic acid

1983 ◽  
Vol 48 (1) ◽  
pp. 304-311 ◽  
Author(s):  
Jiří Křepelka ◽  
Jan Beneš ◽  
Vladimír Pouzar ◽  
Jaroslav Vachek ◽  
Jiří Holubek
Keyword(s):  
Nitrile Group ◽  
Antineoplastic Activity ◽  
Carboxyl Group ◽  
Positional Isomers ◽  
Pentanoic Acid ◽  
Pharmacological Tests ◽  
Derivatives Of

Condensation of triethyl ester of 1,1,5-pentanetricarboxylic acid (XI) with substituted guanidines XXII - XXIX gave acids II - IX, which were converted into esters XI - XIX. The acid II and the ester XI were obtained as mixtures of positional isomers. Analogously, condensation of the triester XXI with dicyanodiamide gave rise to acid X, whose nitrile group, under conditions of esterification of a carboxyl group, produced iminoether XX. In pharmacological tests for antineoplastic activity the compounds prepared exhibited weaker efficacy than 5-(2-amino-6-hydroxy-4-oxo-3,4-dihydro-5-pyrimidinyl)pentanoic acid (I), employed as standard.

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