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Journal articles on the topic 'Oxyma'

Author: Grafiati

Published: 4 June 2021

Last updated: 18 February 2022

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1

El-Faham, Ayman, Fernando Albericio, Srinivasa Rao Manne, and Beatriz G. de la Torre. "OxymaPure Coupling Reagents: Beyond Solid-Phase Peptide Synthesis." Synthesis 52, no. 21 (2020): 3189–210. http://dx.doi.org/10.1055/s-0040-1706296.

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AbstractOxymaPure [ethyl 2-cyano-2-(hydroxyimino)acetate] is an exceptional reagent with which to suppress racemization and enhance coupling efficiency during amide bond formation. The tremendous popularity of OxymaPure has led to the development of several Oxyma-based reagents. OxymaPure and its derived reagents are widely used in solid- and solution-phase peptide chemistry. This review summarizes the recent developments and applications of OxymaPure and Oxyma-based reagents in peptide chemistry, in particular in solution-phase chemistry. Moreover, the side reaction associated with OxymaPure

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2

Jad, Yahya E., Sherine N. Khattab, Beatriz G. de la Torre, et al. "Oxyma-B, an excellent racemization suppressor for peptide synthesis." Org. Biomol. Chem. 12, no. 42 (2014): 8379–85. http://dx.doi.org/10.1039/c4ob01612b.

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3

Burugupalli, Satvika, Sayali Shah, Phillip L. van der Peet, Seep Arora, Jonathan M. White, and Spencer J. Williams. "Investigation of benzoyloximes as benzoylating reagents: benzoyl-Oxyma as a selective benzoylating reagent." Organic & Biomolecular Chemistry 14, no. 1 (2016): 97–104. http://dx.doi.org/10.1039/c5ob02092a.

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4

Jad, Yahya E., Sherine N. Khattab, Beatriz G. de la Torre, et al. "EDC·HCl and Potassium Salts of Oxyma and Oxyma-B as Superior Coupling Cocktails for Peptide Synthesis." European Journal of Organic Chemistry 2015, no. 14 (2015): 3116–20. http://dx.doi.org/10.1002/ejoc.201500142.

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5

Jad, Yahya E., Sherine N. Khattab, Beatriz G. de la Torre, et al. "ChemInform Abstract: EDC·HCl and Potassium Salts of Oxyma and Oxyma-B as Superior Coupling Cocktails for Peptide Synthesis." ChemInform 46, no. 33 (2015): no. http://dx.doi.org/10.1002/chin.201533238.

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6

Jad, Yahya E., Beatriz G. de la Torre, Thavendran Govender, Hendrik G. Kruger, Ayman El-Faham, and Fernando Albericio. "Oxyma-T, expanding the arsenal of coupling reagents." Tetrahedron Letters 57, no. 31 (2016): 3523–25. http://dx.doi.org/10.1016/j.tetlet.2016.06.109.

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7

Kumar, Ashish, Yahya E. Jad, Ayman El-Faham, Beatriz G. de la Torre, and Fernando Albericio. "Diethylphosphoryl-OxymaB (DEPO-B) as a Solid Coupling Reagent for Amide Bond Formation." Letters in Organic Chemistry 16, no. 1 (2018): 30–33. http://dx.doi.org/10.2174/1570178615666180612074420.

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A new phosphonium based coupling reagent DEPO-B has been synthesized from 5- (hydroxyimino)-1,3-dimethylpyrimidine-2,4,6 (1H,3H,5H)-trione (Oxyma B) and diethyl chlorophosphate in presence of base. It is a solid material and the hydrolytic stability and solubility was evaluated for confirming its capability for usage in automated peptide synthesizer.

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8

Mitachi, Katsuhiko, Yuki E. Kurosu, Brandon T. Hazlett, and Michio Kurosu. "Oxyma-based phosphates for racemization-free peptide segment couplings." Journal of Peptide Science 22, no. 3 (2016): 186–91. http://dx.doi.org/10.1002/psc.2859.

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9

Wang, Fengliang, Ling Xu, Guochao Chu, Jing Shi, and Qingxiang Guo. "Efficient Synthesis of Liraglutide by Using Oxyma as Coupling Reagent." Chinese Journal of Organic Chemistry 36, no. 1 (2016): 218. http://dx.doi.org/10.6023/cjoc201505014.

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10

Erny, Marion, Marika Lundqvist, Jon H. Rasmussen, Olivier Ludemann-Hombourger, Frédéric Bihel, and Jan Pawlas. "Minimizing HCN in DIC/Oxyma-Mediated Amide Bond-Forming Reactions." Organic Process Research & Development 24, no. 7 (2020): 1341–49. http://dx.doi.org/10.1021/acs.oprd.0c00227.

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11

Subirós-Funosas, Ramon, Ayman El-Faham, and Fernando Albericio. "PyOxP and PyOxB: the Oxyma-based novel family of phosphonium salts." Organic & Biomolecular Chemistry 8, no. 16 (2010): 3665. http://dx.doi.org/10.1039/c003719b.

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12

Subiros-Funosas, Ramon, Sherine N. Khattab, Lidia Nieto-Rodriguez, Ayman El-Faham, and Fernando Albericio. "ChemInform Abstract: Advances in Acylation Methodologies Enabled by Oxyma-Based Reagents." ChemInform 45, no. 44 (2014): no. http://dx.doi.org/10.1002/chin.201444273.

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13

Wang, Qinghui, Yong Wang, and Michio Kurosu. "A New Oxyma Derivative for Nonracemizable Amide-Forming Reactions in Water." Organic Letters 14, no. 13 (2012): 3372–75. http://dx.doi.org/10.1021/ol3013556.

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14

Cherkupally, Prabhakar, Gerardo A. Acosta, Lidia Nieto-Rodriguez, et al. "K-Oxyma: a Strong Acylation-Promoting, 2-CTC Resin-Friendly Coupling Additive." European Journal of Organic Chemistry 2013, no. 28 (2013): 6372–78. http://dx.doi.org/10.1002/ejoc.201300777.

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15

Caporale, Andrea, Nunzianna Doti, Annamaria Sandomenico, and Menotti Ruvo. "Evaluation of combined use of Oxyma and HATU in aggregating peptide sequences." Journal of Peptide Science 23, no. 4 (2017): 272–81. http://dx.doi.org/10.1002/psc.2977.

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16

Soliman, Saied M., Hazem A. Ghabbour, Sherine N. Khattab, Mohammed R. H. Siddiqui, and Ayman El-Faham. "Synthesis, crystallographic characterization, DFT and TD-DFT studies of Oxyma-sulfonate esters." Journal of Chemical Sciences 129, no. 9 (2017): 1469–81. http://dx.doi.org/10.1007/s12039-017-1354-7.

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17

Jad, Yahya, Sherine Khattab, Beatriz de la Torre, et al. "TOMBU and COMBU as Novel Uronium-Type Peptide Coupling Reagents Derived from Oxyma-B." Molecules 19, no. 11 (2014): 18953–65. http://dx.doi.org/10.3390/molecules191118953.

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18

Kumar, Thoota Sandeep, Alice R. Robert, Himavathi Ganja, Pamerla Muralidhar, Kerru Nagaraju, and Suresh Maddila. "Purification free, chemoselective N-acylation of non-nucleophilic nitrogen heterocycles using oxyma and benzotriazole activations." Chemical Data Collections 32 (April 2021): 100654. http://dx.doi.org/10.1016/j.cdc.2021.100654.

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19

McFarland, Adam D., Jonas Y. Buser, Matthew C. Embry, Charles B. Held, and Stanley P. Kolis. "Generation of Hydrogen Cyanide from the Reaction of Oxyma (Ethyl Cyano(hydroxyimino)acetate) and DIC (Diisopropylcarbodiimide)." Organic Process Research & Development 23, no. 9 (2019): 2099–105. http://dx.doi.org/10.1021/acs.oprd.9b00344.

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20

Chandra, Jyoti, Rohit Chaudhuri, Srinivasa Rao Manne, Sandip Mondal, and Bhubaneswar Mandal. "Direct Synthesis of Sulphonates of Alcohol, Oxyma-O -sulphonates and Oxime-O -sulphonates under Microwave Irradiation." ChemistrySelect 2, no. 27 (2017): 8471–77. http://dx.doi.org/10.1002/slct.201701554.

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21

Palakurthy, Nani Babu, Dharm Dev, Shubhasmin Rana, Krishna Chaitanya Nadimpally, and Bhubaneswar Mandal. "Sulfonamide Synthesis via Oxyma-O-sulfonates - Compatibility to Acid Sensitive Groups and Solid-Phase Peptide Synthesis." European Journal of Organic Chemistry 2013, no. 13 (2013): 2627–33. http://dx.doi.org/10.1002/ejoc.201201571.

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22

Robert, Alice R., Ganta Ravi Kumar, Thoota Sandeep Kumar, Suresh Maddila, and Sreekantha B. Jonnalagadda. "A novel use of Boc-Oxyma as reagent for tert‑butoxycarbonylation of amines and amino acid esters." Chemical Data Collections 30 (December 2020): 100592. http://dx.doi.org/10.1016/j.cdc.2020.100592.

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23

Palakurthy, Nani Babu, Dharm Dev, Shubhasmin Rana, Krishna Chaitanya Nadimpally, and Bhubaneswar Mandal. "ChemInform Abstract: Sulfonamide Synthesis via Oxyma-O-sulfonates - Compatibility to Acid Sensitive Groups and Solid-Phase Peptide Synthesis." ChemInform 44, no. 40 (2013): no. http://dx.doi.org/10.1002/chin.201340075.

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24

Maharani, Rani, Eka Fitri Yanti, M. Devia Irma Melati, and Daniel Sihotang. "Synthesis of Trypsin-modulating Oostatic Factor (TMOF) and its Analogues by Solid-phase Peptide Synthesis Using DIC/Oxyma as Coupling Reagent." Procedia Chemistry 17 (2015): 125–31. http://dx.doi.org/10.1016/j.proche.2015.12.124.

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25

SubirÃ³s-Funosas, Ramon, Rafel Prohens, Rafael Barbas, Ayman El-Faham, and Fernando Albericio. "Oxyma: An Efficient Additive for Peptide Synthesis to Replace the Benzotriazole-Based HOBt and HOAt with a Lower Risk of Explosion[1]." Chemistry - A European Journal 15, no. 37 (2009): 9394–403. http://dx.doi.org/10.1002/chem.200900614.

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26

Thalluri, Kishore, Krishna Chaitanya Nadimpally, Maharishi Parasar Chakravarty, Ashim Paul, and Bhubaneswar Mandal. "ChemInform Abstract: Ethyl 2-(tert-Butoxycarbonyloxyimino)-2-cyanoacetate (Boc-Oxyma) as Coupling Reagent for Racemization-Free Esterification, Thioesterification, Amidation and Peptide Synthesis." ChemInform 44, no. 30 (2013): no. http://dx.doi.org/10.1002/chin.201330049.

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27

Manne, Srinivasa Rao, Kishore Thalluri, Rajat Subhra Giri, Jyoti Chandra, and Bhubaneswar Mandal. "Ethyl 2-(tert-Butoxycarbonyloxyimino)-2-cyanoacetate (Boc-Oxyma): An Efficient Reagent for the Racemization Free Synthesis of Ureas, Carbamates and Thiocarbamates via Lossen Rearrangement." Advanced Synthesis & Catalysis 359, no. 1 (2016): 168–76. http://dx.doi.org/10.1002/adsc.201600661.

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28

Subirós-Funosas, Ramon, Ayman El-Faham, and Fernando Albericio. "Use of Oxyma as pH modulatory agent to be used in the prevention of base-driven side reactions and its effect on 2-chlorotrityl chloride resin." Biopolymers 98, no. 2 (2011): 89–97. http://dx.doi.org/10.1002/bip.21713.

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29

Caporale, A., N. Doti, A. Monti, A. Sandomenico, and M. Ruvo. "Automatic procedures for the synthesis of difficult peptides using oxyma as activating reagent: A comparative study on the use of bases and on different deprotection and agitation conditions." Peptides 102 (April 2018): 38–46. http://dx.doi.org/10.1016/j.peptides.2018.02.006.

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30

Khattab, Sherine Nabil. "Sulfonate Esters of 1-Hydroxypyridin-2(1H)-one and Ethyl 2-Cyano-2-(hydroxyimino)acetate (Oxyma) as Effective Peptide Coupling Reagents to Replace 1-Hydroxybenzotriazole and 1-Hydroxy-7-azabenzotriazole." CHEMICAL & PHARMACEUTICAL BULLETIN 58, no. 4 (2010): 501–6. http://dx.doi.org/10.1248/cpb.58.501.

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31

Khattab, Sherine N. "ChemInform Abstract: Ethyl 2-Cyano-2-(hydroxyimino)acetate (Oxyma): An Efficient and Convenient Additive Used with Tetramethylfluoroformamidinium Hexafluorophosphate (TFFH) to Replace 1-Hydroxybenzotriazole (HOBt) and 1-Hydroxy-7-azabenzotriazole (HOAt) D." ChemInform 42, no. 6 (2011): no. http://dx.doi.org/10.1002/chin.201106203.

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32

Khattab, Sherine N. "Ethyl 2-Cyano-2-(hydroxyimino)acetate (Oxyma): An Efficient and Convenient Additive Used with Tetramethylfluoroformamidinium Hexafluorophosphate (TFFH) to Replace 1-Hydroxybenzotriazole (HOBt) and 1-Hydroxy-7-azabenzotriazole (HOAt) during Peptide Synthesis." Bulletin of the Chemical Society of Japan 83, no. 11 (2010): 1374–79. http://dx.doi.org/10.1246/bcsj.20100075.

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33

Khattab, Sherine Nabil. "ChemInform Abstract: Sulfonate Esters of 1-Hydroxypyridin-2(1H)-one and Ethyl 2-Cyano-2-(hydroxyimino)acetate (Oxyma) as Effective Peptide Coupling Reagents to Replace 1-Hydroxybenzotriazole and 1-Hydroxy-7-azabenzotriazole." ChemInform 41, no. 39 (2010): no. http://dx.doi.org/10.1002/chin.201039194.

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34

Lou, Jiangfei, Jinfang Zhang, Dan Wang, and Xuerong Fan. "Improving the Dyeability and Anti-Wrinkle Properties of Cotton Fabric via Oxidized Raffinose." Applied Sciences 11, no. 10 (2021): 4641. http://dx.doi.org/10.3390/app11104641.

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In the anti-wrinkle finishing of cotton fabrics, the decreased dyeability of the finished fabrics has always been a difficult problem. A new anti-wrinkle finishing mode was developed to solve this problem by changing the finishing sequence of fabric dyeing and anti-wrinkle. In this research, the partial oxidization of raffinose with sodium periodate generated multiple aldehydes, which acted as multifunctional cross-linkers and endowed cotton fabrics with anti-wrinkle and hydrophilic properties. The structural characteristics of oxyRa were analyzed by FTIR and 13C-NMR. Through response surface

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35

YIN, XIANG-CHU, HONG YIN, and JING-YU ZHENG. "A new species and key to known species of genus Oxya Serville (Orthoptera: Acrididae: Catantopinae) from China." Zootaxa 1683, no. 1 (2008): 63. http://dx.doi.org/10.11646/zootaxa.1683.1.5.

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During routine identification of the grasshoppers of the Dasa river, Guizhou Province of China in 2004, a new species [Oxya guizhouensis sp, nov.] of the genus Oxya Serville (Orthoptera, Acrididae, Catantopinae) was discovered. It is described here. A key to all known species of the genus from China is given. The type specimens are deposited in the Museum of Hebei University (MHU), Baoding, Hebei, China.

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36

Yama, Danie Indra, Jojon Soesatrijo, and Rusnadi Santiko. "UJI PENDAHULUAN EFEKTIVITAS BIOINSEKTISIDA AKAR TUBA TERHADAP HAMA Oxya chinensis PADA SKALA LABORATORIUM." Bioscientist : Jurnal Ilmiah Biologi 7, no. 1 (2019): 1. http://dx.doi.org/10.33394/bjib.v7i1.2355.

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The aim of this research is to knowtime of death, mortality and changes in behavior of Oxya chinensis in the treatment of botanical insecticides root of the tuba. The research was conducted at Laboratory Citra Widya Edukasi Palm Oil Polytechnic in Bekasi, the experimental design was the Completely Randomized Design, the treatment consisted of A0 = deltamethrin 0.3 cc/100 ml, A1 = tuba root extract 3g/100ml, A2 = tuba root extract 4g/100ml , A3 = tuba root extract 5g/100ml. Each treatment was repeated three times and each replication contained of 3 samples. Data were analyzed using variance wit

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37

ZHANG, Jian-zhen, Min ZHANG, Ya-ping GUO, and En-bo MA. "Analysis on Genetic Relationship of Oxya chinensis and Oxya japonica from Xuzhou and Pingshan, China." Agricultural Sciences in China 5, no. 2 (2006): 116–22. http://dx.doi.org/10.1016/s1671-2927(06)60028-x.

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38

HUANG, JIANHUA, ZHEMIN ZHENG, YUAN HUANG, and SHANYI ZHOU. "New synonymies in Chinese Oxyinae (Orthoptera: Acrididae)." Zootaxa 1976, no. 1 (2009): 39–55. http://dx.doi.org/10.11646/zootaxa.1976.1.3.

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The genera Oxyoides Zheng & Fu, 1994, Yinia Liu & Li, 1995 and Caryandoides Zheng & Xie, 2007 are revised. As a result of the revision, the genus Oxyoides is synonymized with Oxya Audinet-Serville, 1831, and the genus Caryandoides is synonymized with Yinia. As for the three known members of Oxyoides, the type species Oxyoides wulingshanensis Zheng & Fu, 1994 is proposed as a new junior synonym of Oxya agavisa Tsai, 1931, the two other members, i.e. Oxyoides bamianshanensis Fu & Zheng, 1999 and Oxyoides longianchorus Huang, Fu & Zhou, 2007, are referred to the genus Yini

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39

Pietralonga, Tiago Cetto, Simone Queiroga Brito Gonçalves, Tanos Celmar Costa França, and Arlan da Silva Gonçalves. "ESTUDO COMPUTACIONAL DE REATIVADORES DA ACETILCOLINESTERASE INIBIDA PELO PESTICIDA AGRÍCOLA FENAMIFÓS." Revista Ifes Ciência 1, no. 2 (2015): 51–64. http://dx.doi.org/10.36524/ric.v1i2.306.

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Neste trabalho, foram obtidas, através da técnica de ancoramento molecular, as melhores energias de interação receptor-ligante, além das interações entre cinco oximas conhecidas e a acetilcolinesterase (AChE) de camundongo, inibida pelo pesticida fenamifós. Resultados mostraram que a oxima mais eficiente, in silico, foi a melhor em comparação com dados experimentais da literatura, onde o pesticida usado foi o paraoxon, muito similar ao fenamifós.

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40

Li, L., X. Song, Z. Yin, R. Jia, and Y. Zou. "Insecticidal activities and mechanism of extracts from neem leaves against Oxya chinensis." Arquivo Brasileiro de Medicina Veterinária e Zootecnia 71, no. 1 (2019): 1–10. http://dx.doi.org/10.1590/1678-4162-8958.

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ABSTRACT In this study, neem leaves were successively extracted with petroleum ether, 95% ethanol and water and the insecticidal activities of these extracts against Oxya chinensis larvae were measured. The results showed that 95% ethanol extract gave the highest extraction yield and insecticidal activity, and it was further extracted with five different solvents. The petroleum ether extract from the 95% ethanol extract possessed the highest insecticidal activity with median lethal concentration values ranging from 14.93 to 55.66mg/mL. The gas chromatography-mass spectrometer analysis showed t

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41

Zhu, Dao Hong, and Yoshikazu Ando. "Parthenogenesis in Three Species of Genus Oxya." Japanese journal of applied entomology and zoology 42, no. 2 (1998): 65–69. http://dx.doi.org/10.1303/jjaez.42.65.

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42

Zhang, C., and Y. Huang. "Complete mitochondrial genome of Oxya chinensis (Orthoptera, Acridoidea)." Acta Biochimica et Biophysica Sinica 40, no. 1 (2008): 7–18. http://dx.doi.org/10.1111/j.1745-7270.2008.00375.x.

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43

Hübnerová, Petra, Petr Mlčák, Irena Šínová, Marta Karhanová, and Martin Šín. "Current Use of Automatic Retinal Oximetry – a Review." Czech and Slovak Ophthalmology 76, no. 1 (2020): 3–11. http://dx.doi.org/10.31348/2020/1.

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Purpose: To inform about possible use of the automatic retinal oximetry for the retinal oxygen saturation measurement in the eye and systemic diseases. Methods: We performed a literature review dealing with issues of retinal oxygen saturation monitoring by dual non-invasive retinal oximetry Oxymap T1 (Oxymap ehf. Reykjavík, Iceland). Results: We have found two main strains writing our paper on retinal oxygen saturation eye diseases. The first section concerns diseases created by having hypoxia as its main pathological factor - for example diabetes mellitus and retinal vein occlusion. The secon

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44

Eber, Sabine, Roland Brandl, and Stefan Vidal. "Genetic and morphological variation among populations of Oxyna parietina (Diptera: Tephritidae) across a European transect." Canadian Journal of Zoology 70, no. 6 (1992): 1120–28. http://dx.doi.org/10.1139/z92-157.

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Genetic and morphological variation in the phytophagous tephritid Oxyna parietina (L.) was investigated across a transect through Central Europe by starch-gel electrophoresis to detect allozyme variation and by wing morphometrics. Very low allozyme differentiation was found on both a local and a regional scale, and is best explained by high rates and distances of gene flow. Nevertheless, there exists a smooth cline of allele frequencies from northern to southern populations. We tentatively interpret this cline as being a consequence of selection by environmental factors. The morphological patt

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45

Ma, Enbo, Yaping Guo, and Zhemin Zheng. "CYTOTAXONOMIC STUDY OF OXYA SPECIES IN CHINA (ORTHOPTERA: ACRIDOIDEA)." Insect Science 1, no. 2 (1994): 101–9. http://dx.doi.org/10.1111/j.1744-7917.1994.tb00200.x.

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46

LI, Lijun, Fuping LU, Min ZHANG, Yaping GUO, and Enbo MA. "Different survival of chromium-exposed Oxya chinensis among allozyme genotypes." Journal of Environmental Sciences 21, no. 4 (2009): 509–13. http://dx.doi.org/10.1016/s1001-0742(08)62300-1.

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47

Zhang, Xiaomin, and Keshi Zhang. "Cellular response to bacterial infection in the grasshopper Oxya chinensis." Biology Open 8, no. 10 (2019): bio045864. http://dx.doi.org/10.1242/bio.045864.

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48

Usmani, M. Kamil, and S. Adam Shafee. "A revision of the Indian species of Oxya (Acrididae: Oxyinae)." Oriental Insects 19, no. 1 (1985): 311–22. http://dx.doi.org/10.1080/00305316.1985.10433711.

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49

Yoon, Young-Il, Mi Yeon Chung, Jae-Sam Hwang, et al. "Anti-inflammatory Effect of Oxya chinensis sinuosa Ethanol Extract in LPS-induced RAW 264.7 Cells." Journal of Life Science 24, no. 4 (2014): 370–76. http://dx.doi.org/10.5352/jls.2014.24.4.370.

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50

Rahayu, Sri, and Sulistiyawati Sulistiyawati. "Locusts (Acrididae) Diversity in Gunung Bunder Forest Park." Proceeding International Conference on Science and Engineering 1 (October 31, 2017): 49–53. http://dx.doi.org/10.14421/icse.v1.268.

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The aim of this study was to know the grasshopper diversity in Gunung Bunder Forest Park. Sampling plots were done by purposive sampling method. Grasshoppers were catched by a sweeping net and glue trapping. The result of the research were as follows: grasshopper diversity (H'=1.32), the number of individuals (n=1127), dominance index (D=0.4) and the species evenness index (E=0.55). Grasshopper species found are Phlaeoba fumosa, Stenocatantops splendens, Stenocatantops angustifrons, Eucoptacra sp., Chondracris rosea, Valanga nigricornis, Leptacris sp., Gastrimargus marmoratus, Trilophidia annu

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