Статті в журналах з теми "Phosphite esters"
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Koguchi, Shinichi, Aya Mihoya, Yuga Shibuya, Akane Ito, Anna Toyoda, and Makoto Oba. "Aerobic Oxidation of Phosphite Esters to Phosphate Esters by Using an Ionic-Liquid-Supported Organotelluride Reusable Catalyst." Synlett 31, no. 20 (October 16, 2020): 2043–45. http://dx.doi.org/10.1055/s-0040-1706068.
Повний текст джерелаSaady, Mourad, Luc Lebeau, and Charles Mioskowski. "Selective Monodeprotection of Phosphate, Phosphite, Phosphonate, and Phosphoramide Benzyl Esters." Journal of Organic Chemistry 60, no. 9 (May 1995): 2946–47. http://dx.doi.org/10.1021/jo00114a059.
Повний текст джерелаWang, Hui, and Donald J. Graves. "Calcineurin-catalyzed reaction with phosphite and phosphate esters of tyrosine." Biochemistry 30, no. 12 (March 26, 1991): 3019–24. http://dx.doi.org/10.1021/bi00226a006.
Повний текст джерелаAnary-Abbasinejad, Mohammad, Alireza Hassanabadi, and Hossein Anaraki-Ardakani. "One-pot Synthesis of Stable Phosphite Ylides by three component reaction between Acetylenic Esters, Aldehyde Semicarbazones and Tributyl or Triethyl Phosphite." Journal of Chemical Research 2007, no. 8 (August 2007): 455–57. http://dx.doi.org/10.3184/030823407x236372.
Повний текст джерелаSchwetlick, K., T. König, C. Rüger, J. Pionteck, and W. D. Habicher. "Chain-breaking antioxidant activity of phosphite esters." Polymer Degradation and Stability 15, no. 2 (January 1986): 97–108. http://dx.doi.org/10.1016/0141-3910(86)90065-0.
Повний текст джерелаZayed, M. F., Y. O. El-khoshnieh, N. Khir El-din, and L. S. Boulos. "THE REACTION OF PHOSPHITE ESTERS AND TRIS(DIMETHYLAMIN0)PHOSPHINE WITH 1,4- NAPHTHOQUINONEMONOBENZENESULFONIMINE." Phosphorus, Sulfur, and Silicon and the Related Elements 54, no. 1-4 (September 1990): 81–86. http://dx.doi.org/10.1080/10426509008042123.
Повний текст джерелаSAADY, M., L. LEBEAU, and C. MIOSKOWSKI. "ChemInform Abstract: Selective Monodeprotection of Phosphate, Phosphite, Phosphonate, and Phosphoramide Benzyl Esters." ChemInform 26, no. 37 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199537089.
Повний текст джерелаOba, Makoto, Yasunori Okada, Kozaburo Nishiyama, and Wataru Ando. "Aerobic Photooxidation of Phosphite Esters Using Diorganotelluride Catalysts." Organic Letters 11, no. 9 (May 7, 2009): 1879–81. http://dx.doi.org/10.1021/ol900240s.
Повний текст джерелаDrewe, William C., Martin P. Payne, and Richard V. Williams. "Phosphite esters: a novel class of contact allergen." Contact Dermatitis 76, no. 5 (April 7, 2017): 312–14. http://dx.doi.org/10.1111/cod.12704.
Повний текст джерелаLiu, Chunrong, Chung-Min Park, Difei Wang, and Ming Xian. "Phosphite Esters: Reagents for Exploring S-Nitrosothiol Chemistry." Organic Letters 20, no. 24 (December 6, 2018): 7860–63. http://dx.doi.org/10.1021/acs.orglett.8b03393.
Повний текст джерелаMeyer, Thomas G., Axel Fischer, Peter G. Jones, and Reinhard Schmutzler. "Darstellung und Einkristall-Röntgenstrukturanalyse einiger Fluorphosphite und Phosphitester / Preparation and Single Crystal X-Ray Diffraction Study of Some Fluorophosphites and Phosphite Esters." Zeitschrift für Naturforschung B 48, no. 5 (May 1, 1993): 659–71. http://dx.doi.org/10.1515/znb-1993-0516.
Повний текст джерелаJackson, W. Roy, Patrick Perlmutter, and E. Elizabeth Tasdelen. "Chelation control by phosphite esters in rhodium catalysed hydroformylation." Journal of the Chemical Society, Chemical Communications, no. 10 (1990): 763. http://dx.doi.org/10.1039/c39900000763.
Повний текст джерелаOshel, Reed E., Mecheril V. Nandakumar, Sameer Urgaonkar, David G. Hendricker, and John G. Verkade. "Water solubilization of DDGS via derivatization with phosphite esters." Bioresource Technology 99, no. 12 (August 2008): 5193–205. http://dx.doi.org/10.1016/j.biortech.2007.09.036.
Повний текст джерелаSCHROEDER, G., and B. GIERCZYK. "ChemInform Abstract: Synthesis of New Phosphate and Phosphite Esters of C-Lariat Crown Ethers." ChemInform 28, no. 37 (August 3, 2010): no. http://dx.doi.org/10.1002/chin.199737195.
Повний текст джерелаSokolov, Viatcheslav I., Ludmila A. Bulygina, Oleg Ya Borbulevych, and Oleg V. Shishkin. "Cyclopalladation of phenols in the form of mixed phosphite esters." Journal of Organometallic Chemistry 582, no. 2 (June 1999): 246–51. http://dx.doi.org/10.1016/s0022-328x(99)00058-3.
Повний текст джерелаSchwetlick, K., and T. König. "Antioxidant action of phosphite, sulfite and borate esters—A comparison." Polymer Degradation and Stability 24, no. 4 (January 1989): 279–87. http://dx.doi.org/10.1016/0141-3910(89)90038-4.
Повний текст джерелаSobhani, Sara, and Zahra Vahidi. "P-arylation of aryl halides by an environmentally compatible method." Canadian Journal of Chemistry 95, no. 12 (December 2017): 1280–84. http://dx.doi.org/10.1139/cjc-2017-0364.
Повний текст джерелаYuan, Tao, Fei Chen, and Guo-ping Lu. "Direct synthesis of alkynylphosphonates from alkynes and phosphite esters catalyzed by Cu/Cu2O nanoparticles supported on Nb2O5." New Journal of Chemistry 42, no. 16 (2018): 13957–62. http://dx.doi.org/10.1039/c8nj03206h.
Повний текст джерелаBusfield, WK, ID Grice, and ID Jenkins. "The Reaction of Organophosphorus Radicals With Vinyl Acetate and Acrylonitrile in the Presence of an Aminoxyl Radical Scavenger." Australian Journal of Chemistry 48, no. 3 (1995): 625. http://dx.doi.org/10.1071/ch9950625.
Повний текст джерелаBergstrom, Don, Peter та Robert Lind. "Synthesis of (Dicarbonyl)(η5-cyclopentadienyl)Manganese Complex Stabilized Nucleoside Phosphite Esters". Nucleosides, Nucleotides and Nucleic Acids 8, № 5 (1989): 1061–63. http://dx.doi.org/10.1080/07328318908054281.
Повний текст джерелаFu, Xisheng, Lingguo Sun, Xuguang Zhou, Jianchang Li, Bingji Fan, and Tianhui Ren. "Tribochemical behaviors of phosphite esters and their combinations with alkyl amines." Applied Surface Science 357 (December 2015): 1163–70. http://dx.doi.org/10.1016/j.apsusc.2015.09.156.
Повний текст джерелаBergstrom, Don, and Theresa Schmaltz. "Organoiron-mediated alkylation of phosphite esters: synthesis of (dicarbonyl)(.eta.5-cyclopentadienyl)iron-derived nucleoside phosphonate esters." Journal of Organic Chemistry 57, no. 3 (January 1992): 873–76. http://dx.doi.org/10.1021/jo00029a017.
Повний текст джерелаHolý, Antonín, Ivan Rosenberg, and Hana Dvořáková. "Synthesis of N-(2-(2-phosphonylethoxy)ethyl) derivatives of heterocyclic bases." Collection of Czechoslovak Chemical Communications 55, no. 3 (1990): 809–18. http://dx.doi.org/10.1135/cccc19900809.
Повний текст джерелаShearan, Stephen J. I., Enrico Andreoli, and Marco Taddei. "An alternative C–P cross-coupling route for the synthesis of novel V-shaped aryldiphosphonic acids." Beilstein Journal of Organic Chemistry 18 (November 7, 2022): 1518–23. http://dx.doi.org/10.3762/bjoc.18.160.
Повний текст джерелаArsanious, Mona H. N., Yevette A. Issac, and Leila S. Boulos. "Reactions of phosphite esters and trisdialkylaminophosphines with 5-substituted 1,3,4-thiadiazol derivatives." Heteroatom Chemistry 12, no. 7 (2001): 594–601. http://dx.doi.org/10.1002/hc.1090.
Повний текст джерелаPUDOVIK, M. A., L. K. KIBARDINA, and A. N. PUDOVIK. "ChemInform Abstract: Reaction of Pyrocatechol Phosphite Amides with Carboxylic Acid Silyl Esters." ChemInform 24, no. 6 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199306238.
Повний текст джерелаLebelt, Liwia, Iwona E. Głowacka, and Dorota G. Piotrowska. "Synthesis of Four Enantiomers of (1-Amino-3-Hydroxypropane-1,3-Diyl)Diphosphonic Acid as Diphosphonate Analogues of 4-Hydroxyglutamic Acid." Molecules 27, no. 9 (April 22, 2022): 2699. http://dx.doi.org/10.3390/molecules27092699.
Повний текст джерелаHuang, Yuanting, and Qian Chen. "Recent Advances in C(sp3)—H Phosphorylation Based on Secondary Phosphine Oxides and Phosphite Esters." Chinese Journal of Organic Chemistry 41, no. 11 (2021): 4138. http://dx.doi.org/10.6023/cjoc202107044.
Повний текст джерелаMaghsoodlou, Malek Taher, Sayyed Mostafa Habibi-Khorassani, Mahmoud Nassiri, Sayyed Reza Adhamdoust, and Jaber Salehzadeh. "Stable phosphorus ylides and heterocyclic phosphonate esters derivatives synthesised from stereoselective reactions between triphenyl phosphite and activated acetylenic esters." Journal of Chemical Research 2008, no. 2 (February 1, 2008): 79–82. http://dx.doi.org/10.3184/030823408784365342.
Повний текст джерелаLiu, Yunlang, Tingting Zhu, Zuoming Xie, Chen Deng, Xiujuan Qi, Rong Hu, Jinglin Wang, and Jianyi Chen. "Human Exposure to Chlorinated Organophosphate Ester Flame Retardants and Plasticizers in an Industrial Area of Shenzhen, China." International Journal of Environmental Research and Public Health 19, no. 5 (March 7, 2022): 3126. http://dx.doi.org/10.3390/ijerph19053126.
Повний текст джерелаGrün, Alajos, István Greiner та György Keglevich. "The Synthesis of α-Hydroxy- and α-Chlorophosphonic Acid Derivatives Starting from Benzaldehydes and Phosphorous Acid or Dimethyl Phosphite". Current Organic Chemistry 23, № 8 (31 липня 2019): 968–73. http://dx.doi.org/10.2174/1385272823666190611103102.
Повний текст джерелаHudson, Harry R., Ray W. Matthews, Olyemisi O. Shode, Ramon O. Yusuf, Zsuzsa M. Jászay, György Keglevich, Imre Petneházy та Lászlá Töke. "The Interaction of Phosphite Esters with α-Iodoketones in the Presence of Silver Ion". Phosphorus, Sulfur, and Silicon and the Related Elements 75, № 1-4 (лютий 1993): 15–18. http://dx.doi.org/10.1080/10426509308037353.
Повний текст джерелаMuilwijk, Koen F., Paul C. J. Kamer, and Piet W. N. M. van Leeuwen. "A bulky phosphite-modified rhodium catalyst for the hydroformylation of unsaturated fatty acid esters." Journal of the American Oil Chemists' Society 74, no. 3 (March 1997): 223–28. http://dx.doi.org/10.1007/s11746-997-0127-8.
Повний текст джерелаArsanious, Mona H. N., Yevette A. Issac, and Leila S. Boulos. "ChemInform Abstract: Reactions of Phosphite Esters and Trisdialkylaminophosphines with 5-Substituted 1,3,4-Thiadiazole Derivatives." ChemInform 33, no. 13 (May 22, 2010): no. http://dx.doi.org/10.1002/chin.200213173.
Повний текст джерелаKrátký, Martin, Šárka Štěpánková, Neto-Honorius Houngbedji, Rudolf Vosátka, Katarína Vorčáková, and Jarmila Vinšová. "2-Hydroxy-N-phenylbenzamides and Their Esters Inhibit Acetylcholinesterase and Butyrylcholinesterase." Biomolecules 9, no. 11 (November 5, 2019): 698. http://dx.doi.org/10.3390/biom9110698.
Повний текст джерелаPike, Robert D., Bryn A. Reinecke, Megan E. Dellinger, Austin B. Wiles, Jonathan D. Harper, Jenine R. Cole, Kimberly A. Dendramis, Brian D. Borne, Jeffrey L. Harris, and William T. Pennington. "Bicyclic Phosphite Esters from Pentaerythritol and Dipentaerythritol: New Bridging Ligands in Organometallic and Inorganic Chemistry." Organometallics 23, no. 9 (April 2004): 1986–90. http://dx.doi.org/10.1021/om049957r.
Повний текст джерелаGhanbari, Mohammad M. "Three-component reaction between 5,5-diarylthiohydantoins and acetylenic esters in the presence of trialkyl phosphite." Monatshefte für Chemie - Chemical Monthly 142, no. 7 (May 19, 2011): 749–52. http://dx.doi.org/10.1007/s00706-011-0512-8.
Повний текст джерелаSokolov, V. I., and L. A. Bulygina. "New class of pincer ligands: phosphite esters of 1,3-di(hydroxy)arenes in cyclopalladation reaction." Russian Chemical Bulletin 53, no. 10 (October 2004): 2355–56. http://dx.doi.org/10.1007/s11172-005-0134-6.
Повний текст джерелаZamorano-Octaviano, Jenny, Arely Hernández-Martínez, Armando Ortega-Guevara, Irma Linzaga-Elizalde, and Herbert Höpfl. "Linear and cyclic aminomethanephosphonic acid esters derived from benzaldehyde derivatives, 3-aminopropanol, and diethyl phosphite." Heteroatom Chemistry 17, no. 2 (2006): 75–80. http://dx.doi.org/10.1002/hc.20178.
Повний текст джерелаLi, Yan, Jian Zhao, Qing Yu, and Zhong Wei Wang. "Synthesis Study of the Antioxidant of Tetrakis(2,4-di-tert-butyl phenyl)-4,4’-Biphenylenediphosphonite Esters." Advanced Materials Research 581-582 (October 2012): 206–9. http://dx.doi.org/10.4028/www.scientific.net/amr.581-582.206.
Повний текст джерелаJászay, Zsuzsa M., Imre Petneházy, and László Tőoke. "Preparation of Esters and Amides from Carboxylic Acids by Activation with Dialkyl Phosphite-Carbon Tetrachloride Mixture." Synthetic Communications 28, no. 15 (August 1998): 2761–68. http://dx.doi.org/10.1080/00397919808004849.
Повний текст джерелаNada, A. A., N. Khir El-din, S. T. Gaballah, and M. F. Zayed. "THE BEHAVIOR OF TERTIARY PHOSPHITE ESTERS TOWARDS 1,2-DIHYDRO-3,6-PYRIDAZINEDIONES AND 2,3-DIHYDRO-1,4-PHTHALAZINEDIONES." Phosphorus, Sulfur, and Silicon and the Related Elements 119, no. 1 (December 1996): 27–35. http://dx.doi.org/10.1080/10426509608043462.
Повний текст джерелаMEYER, T. G., A. FISCHER, P. G. JONES, and R. SCHMUTZLER. "ChemInform Abstract: Preparation and Single Crystal X-Ray Diffraction Study of Some Fluorophosphites and Phosphite Esters." ChemInform 24, no. 35 (August 31, 2010): no. http://dx.doi.org/10.1002/chin.199335263.
Повний текст джерелаLiu, Xiao-Ning, Wei-Lei Guo, Chuan-Jin Hou, and Xiang-Ping Hu. "New and Efficient Synthesis of 1,3-Dienylphosphonates by Palladium-Catalyzed Substitution of Propargylic Esters to Diethyl Phosphite." Synthetic Communications 43, no. 19 (June 26, 2013): 2622–26. http://dx.doi.org/10.1080/00397911.2012.725795.
Повний текст джерелаShen, Yanchang, та Zenghong Zhang. "Sequential Transformation of Diethyl Phosphite. A Convenient Synthesis of Substituted (E)-3-Alkoxycarbonyl-β,γ-unsaturated Esters". Journal of Chemical Research, № 10 (1998): 642–43. http://dx.doi.org/10.1039/a803769h.
Повний текст джерелаGhanbari, Mohammad M. "ChemInform Abstract: Three-Component Reaction Between 5,5-Diarylthiohydantoins and Acetylenic Esters in the Presence of Trialkyl Phosphite." ChemInform 42, no. 44 (October 6, 2011): no. http://dx.doi.org/10.1002/chin.201144117.
Повний текст джерелаHUDSON, H. R., R. W. MATTHEWS, O. O. SHODE та R. O. YUSUF. "ChemInform Abstract: The Interaction of Phosphite Esters with α-Iodoketones in the Presence of the Silver Ion". ChemInform 24, № 34 (1 вересня 2010): no. http://dx.doi.org/10.1002/chin.199334209.
Повний текст джерелаTole, Tegene T., Johannes H. L. Jordaan та Hermanus C. M. Vosloo. "α-Pyridinyl Alcohols, α,α’-Pyridine Diols, α-Bipyridinyl Alcohols, and α,α’-Bipyridine Diols as Structure Motifs Towards Important Organic Molecules and Transition Metal Complexes". Current Organic Synthesis 17, № 5 (27 липня 2020): 344–66. http://dx.doi.org/10.2174/1570179417666200212111049.
Повний текст джерелаVarhadi, Poonam, Mehejabeen Kotwal, and D. Srinivas. "Zirconium phenyl phosphonate phosphite as a highly active, reusable, solid acid catalyst for producing fatty acid polyol esters." Applied Catalysis A: General 462-463 (July 2013): 129–36. http://dx.doi.org/10.1016/j.apcata.2013.04.043.
Повний текст джерелаJASZAY, Z. M., I. PETNEHAZY, and L. TOKE. "ChemInform Abstract: Preparation of Esters and Amides from Carboxylic Acids by Activation with Dialkyl Phosphite-Carbon Tetrachloride Mixture." ChemInform 29, no. 43 (June 19, 2010): no. http://dx.doi.org/10.1002/chin.199843097.
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