Heat capacities and thermal diffusivities of some n-alkanoic acid methyl esters

2019 ◽  
Vol 130 ◽  
pp. 33-37 ◽  
Author(s):  
Nataliya S. Bogatishcheva ◽  
Mars Z. Faizullin ◽  
Eugene D. Nikitin
Keyword(s):  
Methyl Esters ◽  
Heat Capacities ◽  
Alkanoic Acid ◽  
Acid Methyl ◽  
Thermal Diffusivities

Heat capacities of fatty acid methyl esters from 300 K to 380 K and up to 4.25 MPa

Fuel ◽  
2015 ◽  
Vol 157 ◽  
pp. 240-244 ◽  
Author(s):  
Xiangyang Liu ◽  
Maogang He ◽  
Chao Su ◽  
Xuetao Qi ◽  
Nan Lv
Keyword(s):  
Fatty Acid ◽  
Fatty Acid Methyl Esters ◽  
Methyl Esters ◽  
Heat Capacities ◽  
Acid Methyl

Structure-reactivity trends of C1–C4 alkanoic acid methyl esters

2011 ◽  
Vol 158 (6) ◽  
pp. 1037-1048 ◽  
Author(s):  
Benjamin Akih-Kumgeh ◽  
Jeffrey M. Bergthorson
Keyword(s):  
Methyl Esters ◽  
Alkanoic Acid ◽  
Acid Methyl

scholarly journals Asymmetric Meerwein-Ponndorf-Verley reduction of long chain keto alkanoic acid methyl esters

2007 ◽  
Vol 72 (5) ◽  
pp. 421-427 ◽  
Author(s):  
Çelik Onar ◽  
Belma Hasdemir ◽  
Ayse Yusufoğlu
Keyword(s):  
1H Nmr ◽  
Optical Rotation ◽  
Methyl Esters ◽  
Enantiomeric Excess ◽  
Enantiomeric Purity ◽  
Hydroxy Ester ◽  
Tetradecanoic Acid ◽  
Alkanoic Acid ◽  
Acid Methyl ◽  
Long Chain

3-, 7- and 13-Monoketo tetradecanoic acid methyl esters carrying a keto group at the ends and at the middle of the chain with 14 carbon atoms were reduced by a Meerwein-Ponndorf-Verley reaction in the presence of R-(+)-1,1'-binaphthalene- 2,2'-diol, 1,2:5,6-D-di-O-isopropylidene-D-mannitol and L-(-)-menthol. The highest enantiomeric purity of 65% ee was found for 13-hydroxy ester isomer. The enantiomeric excess was determined by 1H-NMR shift with Eu(tfc)3 and by optical rotation.

Cuticular waxes from the leaves and fruit capsules of eight Papaveraceae species

1996 ◽  
Vol 74 (3) ◽  
pp. 419-430 ◽  
Author(s):  
Reinhard Jetter ◽  
Markus Riederer
Keyword(s):  
Methyl Esters ◽  
Cuticular Wax ◽  
Biosynthetic Pathways ◽  
Cuticular Waxes ◽  
Alkanoic Acid ◽  
Eschscholtzia Californica ◽  
Acid Methyl ◽  
Isomer Composition ◽  
Alkanoic Acids

Cuticular waxes from leaves and fruit capsules of Papaver alpinum sensu Markgr., P. bracteatum Lindl., P. dubium L., P. nudicaule L., P. orientale L., P. rhoeas L., P. somniferum L., and Eschscholtzia californica Cham. were investigated. They consisted of n-alkanes (< 19%), alk-1-ylesters (< 18%), alk-2-ylesters (< 6%), alkanals (< 19%), secondary alkanols (21–71%, mainly nonacosan-10-ol), triglycerides (< 6%), primary alkanols (2–33%), alkanediols (2–23%, mainly isomeric nonacosanediols), alkanoic acids (< 8%), and alkaloids (< 12%). In addition, minor amounts of iso- and anteiso-alkanes, alkanoic acid methyl esters, esters of alkan-10-ols, benzyl- and phenyl-ethylalcohol, triterpenols and phytosterols, ketols, and ketones were detectable. The isomer composition of the secondary alkanols and their alkanediol, ketol, and ketone derivatives is used to deduce the probable sequence of steps in the respective biosynthetic pathways. Keywords: Papaver, Eschscholtzia, Papaveraceae, cuticular wax, secondary alkanols, biosynthesis.

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