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Acid synthesis
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This experiment aimed to synthesize isoamyl acetate and understand preparing ester’s mechanism. The test compounds underwent reflux, distillation, extraction and vacuum filtration. Through an acid, acetic acid could serve as a substrate. This could easily be attacked by isoamyl alcohol, thus producing isoamyl acetate.
4p
thanhtrinhqc
23-08-2014
57
7
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Fatty acids are an important energy source, for they yield over twice as much energy as an equal mass of carbohydrate or protein. In humans, the primary dietary source of fatty acids is triacylglycerols. This lecture will describe the metabolism of fatty acids. The two main components of fatty acid metabolism are β oxidation and fatty acid synthesis. Upon completion of this lecture, you will understand that the fatty-acid breakdown reactions of β oxidation result in the formation of reduced cofactors and acetyl-CoA molecules, which can be further catabolized to release free energy.
64p
zingzing09
21-10-2012
109
11
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Two enzymes control the rearrangement of carbon skeletons which result in the production of Glyceraldehyde-3-phosphate and Fructose-6-phosphate. Transketolase transfers C2 units: TPP requiring enzyme like pyruvate dehydrogenase Transaldolase transfers C3 units: uses a shiffs base with an active lysine group
44p
zingzing09
21-10-2012
54
11
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Tham khảo bài thuyết trình 'chapter 5. lipid metabolism', khoa học tự nhiên, công nghệ sinh học phục vụ nhu cầu học tập, nghiên cứu và làm việc hiệu quả
64p
zingzing09
21-10-2012
63
8
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Aim of the thesis: Synthesis of several derivatives and tubulysin analogues with the replacement of the amino acid methylpipecolic (Mep) at the N-terminal, replacing N,O-acetyl group by methyl group, and researching the role of tubuphenylalanine (Tup) group at the C-terminal.
26p
extraenglish
24-05-2021
18
4
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Synthesis of several derivatives and tubulysin analogues with the replacement of the amino acid methylpipecolic (Mep) at the N-terminal, replacing N,O-acetyl group by methyl group, and researching the role of tubuphenylalanine (Tup) group at the C-terminal .
26p
capheviahe27
23-02-2021
19
5
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The goals of the dissertation: Synthesizing deep eutectic solvents based on choline chloride with the compounds of 2-alkylbenzimidazole/ethylene glycol and determining their structures; using synthetic deep eutectic solvents to enrich and separate Omega-3,6,9 from waste fat in accordance with the facrories’ procedure of processing Vietnamese basa fish for export.
31p
capheviahe27
23-02-2021
29
3
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Synthesis and structural analysis of hydrotalcite bearing benzothiazolylthiosuccinic acid modified by silane; study on corrosion inhibiting ability for steel of hydrotalcite bearing benzothiazolylthiosuccinic acid modified by silane.
31p
capheviahe27
23-02-2021
34
7
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The aims of the dissertation are: Isolation and purification of the main chemical constituents of the plant Centella asiatica (L.) Urban collected from various regions in Vietnam; synthesis of new derivatives of asiatic acid and madecassic acid obtained from C. asiatica.
27p
capheviahe27
23-02-2021
35
3
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This method is associated with some attractive characteristics such as good selectivity, very short reaction time, high yield of products, cleaner reaction profile,no harmful by-product, cheap and environmental benign catalyst, simple experimental andwork-up procedure. This procedure does not require solvent separation and purification stepssuch as column chromatography.
10p
tocectocec
25-05-2020
15
4
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In this investigation, neodymium orthoferrite (NdFeO3) nanoparticles has been synthesized through ultrasonic method in the presence of octanoic acid as surfactant. This method comparing to the other methods is very fast and it does not need high temperatures during the reaction.
8p
tocectocec
25-05-2020
4
1
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Pirochromite (MgCr2O4) nanoparticles were successfully prepared in this study. During synthesis of the pirochromite nanoparticles, a sol-gel was prepared by using magnesium acetate and potassium dichromate as magnesium and chromium sources and by using stearic acid as the network.
8p
tocectocec
25-05-2020
10
3
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The study revealed that the tested compounds are moderate UVB absorbers, but could be used to augment the effect of other photoprotective agents. Their SPF values were in the range from 3.63 to 4.26 for salicylates 3a-d and from 3.03 to 3.51 for vanillates.
10p
tocectocec
25-05-2020
12
3
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Synthesis of pyrano-chromenes and pyrano-pyrans was developed by three-component reactions of kojic acid and aromatic aldehydes with dimethone and malononitrile, catalyzed with nano-Bi2O3-ZnO and nano-ZnO, respectively.
12p
tocectocec
25-05-2020
14
2
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A fast and facile one-pot procedure for the preparation of symmetric 5-Aryloyl-1,9-dimethyl-5,9-dihydro-2H-pyrano[2,3-d:6,5-d']dipyrimidine-2,4,6,8(1H,3H,7H)-tetraone derivatives by two-component reaction of N-methylbarbituric acid and arylglyoxalmonohydrates catalyzed by DABCO in ethanol at 50 ºC is described.
14p
tocectocec
25-05-2020
13
1
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Pentyl 2-(1H-indole-2-carboxamido)benzoate (5) is obtained in good yield as stable crystals by reaction of pentyl 2-amino benzoate (6) with indole-2-carbonyl chloride acid (7) in the presence of pyridine. The crystal structure of 5 confirms the presence of intramolecular hydrogen bonding (N-H…O) which produces a six-membered ring, and the molecules are linked together by intermolecular hydrogen forces (N-H…O).
6p
tocectocec
25-05-2020
9
1
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An environmentally benign aqueous protocol for the synthesis of novel 2-((5-(4-methoxybenzylidene)-4-oxo-4,5-dihydrothiazol-2-yl)amino)substituted acid by using potassium carbonate as a base has been achieved.
14p
tocectocec
25-05-2020
10
0
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A total synthesis of cyclodepsipeptide [Leu]6-aureobasidin K using combination of solid- and solution-phase
6p
tocectocec
25-05-2020
19
0
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The process described herein proceeds to obtaining diclofenac choline from choline bicarbonate and diclofenac acid in mild conditions, using non-toxic solvent, with the same impurity profile deriving from diclofenac particle as for diclofenac sodium EP.
8p
tocectocec
25-05-2020
9
2
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The total synthesis of mycophenolic acid (MPA), a potent immunosuppressant, was modified. The obtained mycophenolic acid was suitable for further preparation of new prospective immunosuppressants with improved therapeutic properties.
8p
tocectocec
25-05-2020
30
1
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CHỦ ĐỀ BẠN MUỐN TÌM
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