Synthesis of Ortho Acid Ester-Type 1,3-Dioxolanofullerenes: Radical Reaction of [60]Fullerene with Halocarboxylic Acids Promoted by Lead(IV) Acetate

2014 ◽  
Vol 79 (22) ◽  
pp. 11155-11160 ◽  
Author(s):  
Xun You ◽  
Fa-Bao Li ◽  
Guan-Wu Wang
Keyword(s):  
Acid Ester ◽  
Radical Reaction ◽  
Halocarboxylic Acids

scholarly journals Radical Reaction of Unsaturated Acid Ester with Bromoacetonitrile

1966 ◽  
Vol 15 (2) ◽  
pp. 54-58
Author(s):  
Shizuyoshi SAKAI ◽  
Akitada GOTO ◽  
Yoshio ISHII
Keyword(s):  
Unsaturated Acid ◽  
Acid Ester ◽  
Radical Reaction

The Structure of Radiation Cross-Linked Poly (ethylene oxide) Gels

1971 ◽  
Vol 29 ◽  
pp. 76-77
Author(s):  
C. E. Cluthe ◽  
G. G. Cocks
Keyword(s):  
Molecular Weight ◽  
Ethylene Oxide ◽  
Parallel Plate ◽  
Average Molecular Weight ◽  
Radical Reaction ◽  
Free Radical Reaction ◽  
Nitrogen Gas ◽  
Poly Ethylene Oxide ◽  
Poly Ethylene ◽  
Initial Viscosity

Aqueous solutions of a 1 weight-per cent poly (ethylene oxide) (PEO) were degassed under vacuum, transferred to a parallel plate viscometer under a nitrogen gas blanket, and exposed to Co60 gamma radiation. The Co60 source was rated at 4000 curies, and the dose ratewas 3.8x105 rads/hr. The poly (ethylene oxide) employed in the irradiations had an initial viscosity average molecular weight of 2.1 x 106.The solutions were gelled by a free radical reaction with dosages ranging from 5x104 rads to 4.8x106 rads.

XP-23829, a Novel Fumaric Acid Ester, is Efficacious in Reducing Psoriatic Lesions: Results from a Phase 2 Randomized Controlled Study

2017 ◽  
Vol 1 ◽  
pp. s33 ◽  
Author(s):  
Alice B Gottlieb ◽  
Caitriona Ryan ◽  
Richard Kim ◽  
Aftab Alam ◽  
Sagar Munjal ◽  
...  
Keyword(s):  
Fumaric Acid ◽  
Acid Ester ◽  
Randomized Controlled Study ◽  
Controlled Study ◽  
Phase 2 ◽  
Randomized Controlled ◽  
Fumaric Acid Ester ◽  
Psoriatic Lesions

Abstract Not Available

Eco-Friendly Synthesis of Peptides Using Fmoc-Amino Acid Chlorides as Coupling Agent Under Biphasic Condition

2020 ◽  
Vol 27 ◽  
Author(s):  
Santosh Y. Khatavi ◽  
K. Kantharaju
Keyword(s):  
Amino Acid ◽  
Acid Chloride ◽  
Acid Ester ◽  
Analytical Techniques ◽  
Peptide Bond ◽  
Amino Acid Ester ◽  
Acid Chlorides ◽  
Peptide Bond Formation ◽  
Green Protocol ◽  
Additional Base

Background: Agro-waste derived solvent media act as a greener process for the peptide bond formation using Nα - Fmoc-amino acid chloride and amino acid ester salt with in situ neutralization and coupling under biphasic condition. The Fmoc-amino acid chlorides are prepared by the reported procedure of freshly distilled SOCl2 with dry CH2Cl2. The protocol found many added advantages such as neutralization of amino acid ester salt and not required additional base for the neutralization, and directly coupling take place with Fmoc-amino acid chloride gave final product dipeptide ester in good to excellent yields. The protocol occurs with complete stereo chemical integrity of the configuration of substrates. Here, we revisited Schotten-Baumann condition, instead of using inorganic base. Objective: To develop green protocol for the synthesis of peptide bond using Fmoc-amino acid chloride with amino acid esters salt. Methods: The final product isolated is analyzed in several spectroscopic and analytical techniques such as FT-IR, 1H-, 13CNMR, Mass spectrometry and RP-HPLC to check stereo integrity and purity of the product. Conclusion: The present method developed greener using natural agro-waste (lemon fruit shell ash) derived solvent medium for the reaction and not required chemical entity.

Crystal Violet, an Electronic Model Substance for Rubber and Related Olefins

1951 ◽  
Vol 24 (1) ◽  
pp. 169-181 ◽  
Author(s):  
G. J. van Veersen
Keyword(s):  
Crystal Violet ◽  
Electronic Structures ◽  
Radical Reaction ◽  
Test Tube ◽  
Chemical Agent ◽  
Blue Color ◽  
Electronic Model ◽  
Model Substance ◽  
Model Substances ◽  
Polar Reaction

Abstract It is shown that triphenylmethyl dyes like crystal violet can be used as model substances for rubber and related olefins. Arguments are given in support of the assumption that agents which react with rubber and related olefins in a polar manner cause a reversible shift in color from blue to yellow with crystal violet, whereas a fading of the blue color of crystal violet (if alkaline or reducing agents are excluded) points to a radical reaction. Since the electronic structures of donor olefins and crystal violet are considered and not the molecular structure, as usually is done in the choice of a model substance, these dyes have been named electronic model substances. Though crystal violet, as an electronic model substance cannot be used for the study of the overall reactions, information can often be obtained concerning the first step in a reaction of rubber with a certain chemical agent by means of a simple test-tube reaction with crystal violet. It was pointed out that the π-electron availability at the non-methylated carbon atom of the double bond in rubber and at the nitrogen atoms in crystal violet is probably of the same order. As an application of crystal violet as an electronic model substance for rubber, a polar reaction between sulfur and rubber is suggested as the first step in vulcanization.

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