Dimerization in trans-4-butyl-cyclohexane carboxylic acid and in its mixture with 12% cis-isomer observed via 1H- and 2H-NMR

1998 ◽  
Author(s):  
Sofia I. Torgova ◽  
D. Abramic ◽  
Alfredo Strigazzi ◽  
Slobodan Zumer
Keyword(s):  
Carboxylic Acid ◽  
H Nmr ◽  
In Trans ◽  
Cyclohexane Carboxylic Acid ◽  
Cis Isomer

scholarly journals Enzymes Involved in a Novel Anaerobic Cyclohexane Carboxylic Acid Degradation Pathway

2014 ◽  
Vol 196 (20) ◽  
pp. 3667-3674 ◽  
Author(s):  
J. W. Kung ◽  
A.-K. Meier ◽  
M. Mergelsberg ◽  
M. Boll
Keyword(s):  
Carboxylic Acid ◽  
Degradation Pathway ◽  
Acid Degradation ◽  
Cyclohexane Carboxylic Acid

scholarly journals Functionalization and Chemical Modification of 2-Hydroxyethyl Methacrylate with Carboxylic Acid

2012 ◽  
Vol 9 (3) ◽  
pp. 1135-1144 ◽  
Author(s):  
Mohammad Hossein Nasirtabrizi ◽  
L. Zargin ◽  
S. Khodabandlou ◽  
S. Rostamzadeh Mansour
Keyword(s):  
Thermal Analysis ◽  
Free Radical ◽  
Carboxylic Acid ◽  
Addition Reaction ◽  
Molar Ratio ◽  
Esterification Reaction ◽  
Hydroxyethyl Methacrylate ◽  
H Nmr ◽  
Temperature Ranges ◽  
Ft Ir

Free radical polymerization of the resulting monomers methyl methacrylate (MMA), ethyl methacrylate (EMA), methylacrylate (MA) and ethylacrylate (EA) with 2-hydroxyethyl methacrylate (HEMA) (in 1:1 mole ratio) were carried out using azobis(isoboutyronitrile) (AIBN) as initiator at the temperature ranges 60-70°C. The modification of polymers were carried out by 9-anthracenecarboxylic acid (9-ACA) via the esterification reaction between —OH of poly(HEMA) and —COOH of 9-ACA, in presence of N,N′-dicyclohexyl-carbodiimide (DCC), 4-(dimethylamino) pyridine (DMAP) and N,N-dimethyl formamid (DMF). It was found that the molar ratio acid/alcohol/catalysts= 0.02: 0.02: 0.02 and 0.002, optimal for preparation of the ester. As demonstrated by FT-IR,1H-NMR and dynamic mechanical thermal analysis (DMTA). The Tg value of methacrylate and acrylate copolymers containing 9-ACA groups was found to increase with incorporation of 9-ACA groups in polymer structures. The presence of 9-ACA groups in the polymer side chains created new polymers with novel modified properties that find some applications in polymer industry. These anthracenic factors could take part in cyclo addition reaction with other factors such as anhydrides and kinons.

scholarly journals Controlling Growth of Common Carpetgrass Using Selected Plant Growth Regulators

HortScience ◽  
1998 ◽  
Vol 33 (4) ◽  
pp. 704-706 ◽  
Author(s):  
Edward W. Bush ◽  
Wayne C. Porter ◽  
Dennis P. Shepard ◽  
James N. McCrimmon
Keyword(s):  
Carboxylic Acid ◽  
Plant Growth ◽  
Plant Growth Regulators ◽  
Growth Regulators ◽  
Acid Ethyl Ester ◽  
Field Studies ◽  
Turf Quality ◽  
Application Rates ◽  
Cyclohexane Carboxylic Acid

Field studies were performed on established carpetgrass (Axonopus affinis Chase) in 1994 and 1995 to evaluate plant growth regulators (PGRs) and application rates. Trinexapac-ethyl (0.48 kg·ha-1) improved turf quality and reduced cumulative vegetative growth (CVG) of unmowed and mowed plots by 38% and 46%, respectively, in 1995, and suppressed seedhead height in unmowed turf by >31% 6 weeks after treatment (WAT) both years. Mefluidide (0.14 and 0.28 kg·ha-1) had little effect on carpetgrass. Sulfometuron resulted in unacceptable phytotoxicity (>20%) 2 WAT in 1994 and 18% phytotoxicity in 1995. In 1995, sulfometuron reduced mowed carpetgrass CVG 21%, seedhead number 47%, seedhead height 36%, clipping yield 24%, and reduced the number of mowings required. It also improved unmowed carpetgrass quality at 6 WAT. Sethoxydim (0.11 kg·ha-1) suppressed seedhead formation by 60% and seedhead height by 20%, and caused moderate phytotoxicity (13%) in 1995. Sethoxydim (0.22 kg·ha-1) was unacceptably phytotoxic (38%) in 1994, but only slightly phytotoxic (7%) in 1995, reduced clipping yields (>24%), and increased quality of mowed carpetgrass both years. Fluazasulfuron (0.027 and 0.054 kg·ha-1) phytotoxicity ratings were unacceptable at 2 WAT in 1994, but not in 1995. Fluazasulfuron (0.054 kg·ha-1) reduced seedhead height by 23% to 26% in both years. Early seedhead formation was suppressed >70% when applied 2 WAT in 1994, and 43% when applied 6 WAT in 1995. The effects of the chemicals varied with mowing treatment and evaluation year. Chemical names used: 4-(cyclopropyl-x-hydroxy-methylene)-3,5 dioxo-cyclohexane-carboxylic acid ethyl ester (trinexapac-ethyl); N-2,4-dimethyl-5-[[(trifluoro-methyl)sulfonyl]amino]phenyl]acetamide] (mefluidide); [methyl 2-[[[[(4,6-dimethyl-2-pyrimidinyl) amino]carbonyl] amino] sulfonyl]benzoate)] (sulfometuron); (2-[1-(ethoxyimino)butyl-5-[(2-ethylthio)propyl]-3-hydroxy-2-cyclohexen-1-one) (sethoxydim); 1-(4,6-dimethoxypyrimidin-2yl)-3-[(3-trifluoromethyl-pyridin 2-yl) sulphonyl] urea (fluazasulfuron).

Synthesis and properties of oxytocin analogues modified in the tripeptide side chain

1984 ◽  
Vol 49 (3) ◽  
pp. 642-652 ◽  
Author(s):  
Zdenko Procházka ◽  
Michal Lebl ◽  
Tomislav Barth ◽  
Jan Hlaváček ◽  
Antonín Trka ◽  
...  
Keyword(s):  
Nmr Spectroscopy ◽  
Carboxylic Acid ◽  
Biological Activities ◽  
The Other ◽  
Side Chain ◽  
H Nmr ◽  
Fragment Condensation

Two oxytocin analogues were synthesized by fragment condensation (6 + 3) in the presence of dicyclohexylcarbodiimide and 1-hydroxybenzotriazole. In one of the analogues, proline in the position 7 and leucine in the position 8 were substituted by 2-[1-(2-oxo-3-aminopyrrolidinyl)]-4-methylpentanoic acid, in the other proline was replaced by 1-aminocyclopropane-1-carboxylic acid. Biological activities of the first analogue were strongly reduced and dissociation of the uterotonic and galoctogogic activities was observed with both the analogues. The structure of 2-(3-tert-butyloxycarbonylaminopyrrolidin-2-on-1-yl)-4-methylpentanoylglycine and its amide was confirmed by mass and 1 H NMR spectroscopy.

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