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Journal articles on the topic 'Chlorohydrin esters'

Author: Grafiati
Published: 4 June 2021
Last updated: 8 February 2022

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1

Eras, Jordi, Jonh Jairo Méndez, Mercè Balcells, and Ramon Canela. "Chlorotrimethylsilane: A Suitable Reagent for the Synthesis of Chlorohydrin Esters." Journal of Organic Chemistry 67, no. 24 (2002): 8631–34. http://dx.doi.org/10.1021/jo026020w.

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2

Makhin, M. N., and M. S. Klebanov. "Reaction Kinetics of Dehydrochlorination of the Chlorohydrin Esters of Bisphenol A." Kinetics and Catalysis 61, no. 2 (2020): 238–41. http://dx.doi.org/10.1134/s0023158420020081.

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3

Villorbina, Gemma, Albert Tomàs, Marc Escribà, et al. "Combining AlCl3·6H2O and an ionic liquid to prepare chlorohydrin esters from glycerol." Tetrahedron Letters 50, no. 23 (2009): 2828–30. http://dx.doi.org/10.1016/j.tetlet.2009.03.183.

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4

Eras, Jordi, Jonh Jairo Méndez, Mercè Balcells, and Ramon Canela. "Influence of Carboxylic Acids on the Synthesis of Chlorohydrin Esters from 1,3‐Butanediol." Synthetic Communications 36, no. 9 (2006): 1167–75. http://dx.doi.org/10.1080/00397910500514055.

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5

Glass, Beverley D., Andr� Goosen, and Cedric W. McCleland. "Reactions of 1,3-dioxolanes with iodine monochloride: formation of chlorohydrin esters and diol monoesters." Journal of the Chemical Society, Perkin Transactions 2, no. 11 (1993): 2175. http://dx.doi.org/10.1039/p29930002175.

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6

Escribà, Marc, Jordi Eras, Miquel Duran, et al. "From glycerol to chlorohydrin esters using a solvent-free system. Microwave irradiation versus conventional heating." Tetrahedron 65, no. 50 (2009): 10370–76. http://dx.doi.org/10.1016/j.tet.2009.10.048.

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7

GLASS, B. D., A. GOOSEN, and C. W. MCCLELAND. "ChemInform Abstract: Reactions of 1,3-Dioxolanes with Iodine Monochloride: Formation of Chlorohydrin Esters and Diol Monoesters." ChemInform 25, no. 6 (2010): no. http://dx.doi.org/10.1002/chin.199406080.

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8

BABAKHANOV, R. A., S. B. ZEINALOV, S. K. SHARIFOVA, M. S. MEKHTIEV та E. A. AGAEVA. "ChemInform Abstract: Synthesis of α-Hydroxy-β-amino-Substituted Esters of Aromatic Carboxylic Acids (V) Based on Their Chlorohydrin Derivatives". ChemInform 25, № 17 (2010): no. http://dx.doi.org/10.1002/chin.199417120.

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9

Jones, AR, and LM Porter. "Inhibition of glycolysis in boar spermatozoa by alpha-chlorohydrin phosphate appears to be mediated by phosphatase activity." Reproduction, Fertility and Development 7, no. 5 (1995): 1089. http://dx.doi.org/10.1071/rd9951089.

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Abstract:
(R,S)-alpha-chlorohydrin-1-phosphate, previously shown to have no anti-glycolytic activity on mature boar sperm in vitro, is a substrate for acid and/or neutral phosphatase(s) that are associated with washed sperm. The high phosphatase activity hydrolyses the ester to alpha-chlorohydrin which undergoes oxidation to (S)-3-chlorolactaldehyde, a specific inhibitor of sperm glyceraldehyde-3-phosphate dehydrogenase and triosephosphate isomerase, thereby exhibiting an anti-glycolytic action.
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10

McManus, S. P., R. M. Karaman, R. Sedaghat-Herati, et al. "Participation by ether oxygen (RO-3) in the hydrolysis of sulfonate esters of 2-methoxyethanol and 2-methoxy-2-methyl-1-propanol. Implications regarding the nonlinear ethanol-trifluoroethanol plot for mustard chlorohydrin." Journal of Organic Chemistry 52, no. 12 (1987): 2518–22. http://dx.doi.org/10.1021/jo00388a032.

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11

Sakhnenko, V. I., Yu V. Pavlov, V. L. Rogachev, et al. "Saftey problems related to the nitration of styrene chlorohydrin methyl ester in semicontinuous reactors." Pharmaceutical Chemistry Journal 22, no. 2 (1988): 160–64. http://dx.doi.org/10.1007/bf00758448.

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12

Yoshimura, Fumihiko, Atsushi Matsui, Atsushi Hirai, Keiji Tanino та Masaaki Miyashita. "Stereoselective SN2′ alkylation reaction sequence of the γ,δ-epoxy α,β-unsaturated ester system via γ,δ-chlorohydrin intermediates by the use of a R3Al–CuCN reagent". Tetrahedron Letters 50, № 36 (2009): 5126–29. http://dx.doi.org/10.1016/j.tetlet.2009.06.106.

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13

Eras, Jordi, Jonh Jairo Mendez, Merce Belcells, and Ramon Canela. "Chlorotrimethylsilane: A Suitable Reagent for the Synthesis of Chlorohydrin Esters." ChemInform 34, no. 18 (2003). http://dx.doi.org/10.1002/chin.200318059.

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14

SOROKIN, M. F., L. G. SHODE, A. I. KUZ'MIN, and L. V. DUDINA. "ChemInform Abstract: Investigation into the Dehydrochlorination of Carboxylic Acid Chlorohydrin Esters." Chemischer Informationsdienst 17, no. 6 (1986). http://dx.doi.org/10.1002/chin.198606086.

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15

Mendez, Jonh Jairo, Jordi Eras, Merce Balcells, and Ramon Canela. "Influence of Carboxylic Acids on the Synthesis of Chlorohydrin Esters from 1,3-Butanediol." ChemInform 37, no. 34 (2006). http://dx.doi.org/10.1002/chin.200634054.

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16

MCMANUS, S. P., R. M. KARAMAN, R. SEDAGHAT-HERATI, et al. "ChemInform Abstract: Participation by Ether Oxygen (RO-3) in the Hydrolysis of Sulfonate Esters of 2-Methoxyethanol and 2-Methoxy-2-methyl-1-propanol. Implications Regarding the Nonlinear Ethanol-Trifluoroethanol Plot for Mustard Chlorohydrin." ChemInform 18, no. 49 (1987). http://dx.doi.org/10.1002/chin.198749137.

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17

Yoshimura, Fumihiko, Atsushi Matsui, Atsushi Hirai, Keiji Tanino, and Masaaki Miyashita. "ChemInform Abstract: Stereoselective SN2′ Alkylation Reaction Sequence of the γ,δ-Epoxy α,β-Unsaturated Ester System via γ,δ-Chlorohydrin Intermediates by the Use of a R3Al—CuCN Reagent." ChemInform 40, no. 49 (2009). http://dx.doi.org/10.1002/chin.200949053.

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