Статті в журналах з теми "Diazo-transfer"
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Russo, Laura, Stefano Zanini, Claudia Riccardi, Francesco Nicotra, and Laura Cipolla. "Diazo transfer for azido-functional surfaces." Materials Today 14, no. 4 (April 2011): 164–69. http://dx.doi.org/10.1016/s1369-7021(11)70088-8.
Повний текст джерелаGhosh, Somnath, and Indira Datta. "Diazo Transfer Reaction in Solid State." Synthetic Communications 21, no. 2 (January 1991): 191–200. http://dx.doi.org/10.1080/00397919108020811.
Повний текст джерелаVillalgordo, Jos� M., Adelheid Enderli, Anthony Linden, and Heinz Heimgartner. "Diazo-Transfer Reaction with Diphenyl Phosphorazidate." Helvetica Chimica Acta 78, no. 8 (December 13, 1995): 1983–98. http://dx.doi.org/10.1002/hlca.19950780807.
Повний текст джерелаJászay, Zsuzsa M., Truong Son Pham, Katalin Gönczi, Imre Petneházy, and László Tőke. "Efficient Solid/Liquid Phase-Transfer Catalytic Diazo Transfer Synthesis." Synthetic Communications 40, no. 11 (May 6, 2010): 1574–79. http://dx.doi.org/10.1080/00397910903100742.
Повний текст джерелаKrasavin, Mikhail, Dmitry Dar’in, Grigory Kantin та Olga Bakulina. "Facile One-Pot Access to α-Diazo-β-ketosulfones from Sulfonyl Chlorides and α-Haloketones". Synthesis 52, № 15 (28 квітня 2020): 2259–66. http://dx.doi.org/10.1055/s-0040-1707525.
Повний текст джерелаTarrant, Elaine, Claire V. O'Brien, and Stuart G. Collins. "Studies towards a greener diazo transfer methodology." RSC Advances 6, no. 37 (2016): 31202–9. http://dx.doi.org/10.1039/c6ra03678c.
Повний текст джерелаLandman, Iris R., Farzaneh Fadaei-Tirani, and Kay Severin. "Nitrous oxide as a diazo transfer reagent: the synthesis of triazolopyridines." Chemical Communications 57, no. 87 (2021): 11537–40. http://dx.doi.org/10.1039/d1cc04907k.
Повний текст джерелаChiang, Yvonne, A. Jerry Kresge, Oleg Sadovski, Xiaofeng Zeng, and Yu Zhu. "Kinetics and mechanism of acid-catalyzed hydrolysis of the diazo functional groups of 1-diazo-2-indanone and 2-diazo-1-indanone in aqueous solution." Canadian Journal of Chemistry 83, no. 9 (September 1, 2005): 1202–6. http://dx.doi.org/10.1139/v05-115.
Повний текст джерелаGreen, Sebastian P., Katherine M. Wheelhouse, Andrew D. Payne, Jason P. Hallett, Philip W. Miller, and James A. Bull. "Thermal Stability and Explosive Hazard Assessment of Diazo Compounds and Diazo Transfer Reagents." Organic Process Research & Development 24, no. 1 (November 28, 2019): 67–84. http://dx.doi.org/10.1021/acs.oprd.9b00422.
Повний текст джерелаPandiakumar, Arun Kumar, Siddhartha P. Sarma, and Ashoka G. Samuelson. "Mechanistic studies on the diazo transfer reaction." Tetrahedron Letters 55, no. 18 (April 2014): 2917–20. http://dx.doi.org/10.1016/j.tetlet.2014.03.057.
Повний текст джерелаKoskinen, Ari M. P., and Luis Muñoz. "Diazo transfer reactions under mildly basic conditions." J. Chem. Soc., Chem. Commun., no. 8 (1990): 652–53. http://dx.doi.org/10.1039/c39900000652.
Повний текст джерелаDeadman, Benjamin J., Rosella M. O'Mahony, Denis Lynch, Daniel C. Crowley, Stuart G. Collins, and Anita R. Maguire. "Taming tosyl azide: the development of a scalable continuous diazo transfer process." Organic & Biomolecular Chemistry 14, no. 13 (2016): 3423–31. http://dx.doi.org/10.1039/c6ob00246c.
Повний текст джерелаWang, Ban, Isaac G. Howard, Jackson W. Pope, Eric D. Conte, and Yongming Deng. "Bis(imino)pyridine iron complexes for catalytic carbene transfer reactions." Chemical Science 10, no. 34 (2019): 7958–63. http://dx.doi.org/10.1039/c9sc02189b.
Повний текст джерелаRamachary, Dhevalapally B., Vidadala V. Narayana, and Kinthada Ramakumar. "Direct ionic liquid promoted organocatalyzed diazo-transfer reactions: diversity-oriented synthesis of diazo-compounds." Tetrahedron Letters 49, no. 17 (April 2008): 2704–9. http://dx.doi.org/10.1016/j.tetlet.2008.02.159.
Повний текст джерелаXie, Shibo, Ziqiang Yan, Yuanheng Li, Qun Song, and Mingming Ma. "Intrinsically Safe and Shelf-Stable Diazo-Transfer Reagent for Fast Synthesis of Diazo Compounds." Journal of Organic Chemistry 83, no. 18 (August 18, 2018): 10916–21. http://dx.doi.org/10.1021/acs.joc.8b01587.
Повний текст джерелаJaszay, Zsuzsa M., Truong Son Pham, Katalin Goenczi, Imre Petnehazy, and Laszlo Toeke. "ChemInform Abstract: Efficient Solid/Liquid Phase-Transfer Catalytic Diazo Transfer Synthesis." ChemInform 41, no. 43 (September 30, 2010): no. http://dx.doi.org/10.1002/chin.201043048.
Повний текст джерелаDasgupta, Ayan, Emma Richards, and Rebecca L. Melen. "Triarylborane Catalyzed Carbene Transfer Reactions Using Diazo Precursors." ACS Catalysis 12, no. 1 (December 17, 2021): 442–52. http://dx.doi.org/10.1021/acscatal.1c04746.
Повний текст джерелаRianelli, Renata de S., Maria Cecília B. V. de Souza, and Vitor F. Ferreira. "Mild Diazo Transfer Reaction Catalyzed by Modified Clays." Synthetic Communications 34, no. 5 (December 31, 2004): 951–59. http://dx.doi.org/10.1081/scc-120028368.
Повний текст джерелаEmpel, Claire, Katharina J. Hock, and Rene M. Koenigs. "Iron-catalysed carbene-transfer reactions of diazo acetonitrile." Organic & Biomolecular Chemistry 16, no. 39 (2018): 7129–33. http://dx.doi.org/10.1039/c8ob01991f.
Повний текст джерелаTaber, Douglass F., Robert E. Ruckle, and Michael J. Hennessy. "Mesyl azide: a superior reagent for diazo transfer." Journal of Organic Chemistry 51, no. 21 (October 1986): 4077–78. http://dx.doi.org/10.1021/jo00371a034.
Повний текст джерелаGHOSH, S., and I. DATTA. "ChemInform Abstract: Diazo Transfer Reaction in Solid State." ChemInform 22, no. 48 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199148101.
Повний текст джерелаVILLALGORDO, J. M., A. ENDERLI, A. LINDEN, and H. HEIMGARTNER. "ChemInform Abstract: Diazo-Transfer Reaction with Diphenyl Phosphorazidate." ChemInform 27, no. 12 (August 12, 2010): no. http://dx.doi.org/10.1002/chin.199612048.
Повний текст джерелаShevalev, Robert M., Petr A. Zhmurov, Dmitry V. Dar’in та Mikhail Krasavin. "Taking diazo transfer to water: α-diazo carbonyl compounds from in situ generated mesyl azide". Mendeleev Communications 30, № 3 (травень 2020): 372–73. http://dx.doi.org/10.1016/j.mencom.2020.05.037.
Повний текст джерелаKuruba, Bharath Kumar, Nusrathulla Shariff, Samuel Vasanthkumar та Lourdusamy Emmanuvel. "NaOH/Et3N-Promoted Stereoselective One-Pot Synthesis ofα-Diazo Oxime Ethers via Diazo Transfer Reaction". Synthetic Communications 45, № 21 (вересень 2015): 2454–61. http://dx.doi.org/10.1080/00397911.2015.1085575.
Повний текст джерелаChiara, Jose Luis, та José Ramón Suárez. "Synthesis of α-Diazo Carbonyl Compounds with the Shelf-Stable Diazo Transfer Reagent Nonafluorobutanesulfonyl Azide". Advanced Synthesis & Catalysis 353, № 4 (2 березня 2011): 575–79. http://dx.doi.org/10.1002/adsc.201000846.
Повний текст джерелаDar’in, Dmitry, Grigory Kantin, and Mikhail Krasavin. "A ‘sulfonyl-azide-free’ (SAFE) aqueous-phase diazo transfer reaction for parallel and diversity-oriented synthesis." Chemical Communications 55, no. 36 (2019): 5239–42. http://dx.doi.org/10.1039/c9cc02042j.
Повний текст джерелаMonteiro, H. J. "Preparation of α-Diazo-β-Ketosulfones by Diazo-Transfer Reaction with Anin situGenerated Azidinium Salt. A Safe and Efficient Procedure for the Diazo-Transfer Reaction in Neutral Medium". Synthetic Communications 17, № 8 (червень 1987): 983–92. http://dx.doi.org/10.1080/00397918708063957.
Повний текст джерелаGonzález-Granda, Sergio, Taíssa A. Costin, Marcus M. Sá та Vicente Gotor-Fernández. "Stereoselective Bioreduction of α-diazo-β-keto Esters". Molecules 25, № 4 (19 лютого 2020): 931. http://dx.doi.org/10.3390/molecules25040931.
Повний текст джерелаDar’in, Dmitry, Grigory Kantin та Mikhail Krasavin. "Practical Application of the Aqueous ‘Sulfonyl-Azide-Free’ (SAFE) Diazo Transfer Protocol to Less α-C–H Acidic Ketones and Esters". Synthesis 51, № 22 (28 серпня 2019): 4284–90. http://dx.doi.org/10.1055/s-0039-1690613.
Повний текст джерелаH. Faialaga, Nathan. "Discussion Addendum for: Detrifluoroacetylative Diazo Group Transfer: (E)-1-Diazo-4-phenyl-3-buten-2-one." Organic Syntheses 99 (2022): 234–50. http://dx.doi.org/10.15227/orgsyn.099.0234.
Повний текст джерелаYan, Ziqiang, Shibo Xie, Yuanheng Li, Qun Song, and Mingming Ma. "Correction to Intrinsically Safe and Shelf-Stable Diazo-Transfer Reagent for Fast Synthesis of Diazo Compounds." Journal of Organic Chemistry 84, no. 11 (May 23, 2019): 7541. http://dx.doi.org/10.1021/acs.joc.9b00914.
Повний текст джерелаTolman, Vladimír, and Petr Sedmera. "Some New Derivatives of 2-Pentenedioic Acid." Collection of Czechoslovak Chemical Communications 58, no. 6 (1993): 1430–36. http://dx.doi.org/10.1135/cccc19931430.
Повний текст джерелаMrówczyński, R., L. Magerusan, R. Turcu, and J. Liebscher. "Diazo transfer at polydopamine – a new way to functionalization." Polym. Chem. 5, no. 22 (July 30, 2014): 6593–99. http://dx.doi.org/10.1039/c4py00670d.
Повний текст джерелаKitamura, Mitsuru, Rie Sakata, Norifumi Tashiro, Azusa Ikegami, and Tatsuo Okauchi. "Synthesis of Diazonaphthoquinones from Naphthols by Diazo-Transfer Reaction." Bulletin of the Chemical Society of Japan 88, no. 6 (June 15, 2015): 824–33. http://dx.doi.org/10.1246/bcsj.20150021.
Повний текст джерелаChiara, Jose Luis, та Jose Ramon Suarez. "ChemInform Abstract: Synthesis of α-Diazo Carbonyl Compounds with the Shelf-Stable Diazo Transfer Reagent Nonafluorobutanesulfonyl Azide." ChemInform 42, № 24 (19 травня 2011): no. http://dx.doi.org/10.1002/chin.201124053.
Повний текст джерелаFructos, Manuel R., M. Mar Díaz-Requejo, and Pedro J. Pérez. "Gold and diazo reagents: a fruitful tool for developing molecular complexity." Chemical Communications 52, no. 46 (2016): 7326–35. http://dx.doi.org/10.1039/c6cc01958g.
Повний текст джерелаMcGuiness, Mark, and Harold Shechter. "Azidotris(diethylamino)phosphonium bromide: A self-catalyzing diazo transfer reagent." Tetrahedron Letters 31, no. 35 (January 1990): 4987–90. http://dx.doi.org/10.1016/s0040-4039(00)97785-2.
Повний текст джерелаCoquerel, Yoann, Jean Rodriguez, Marc Presset, and Damien Mailhol. "Diazo-Transfer Reactions to 1,3-Dicarbonyl Compounds with Tosyl Azide." Synthesis 2011, no. 16 (July 14, 2011): 2549–52. http://dx.doi.org/10.1055/s-0030-1260107.
Повний текст джерелаAdam, Waldemar, and Elena Gonzalez Nuñez. "Oxygen transfer by dissociative electron transfer. Reaction of tetranitromethane with diazo compounds and sulfides." Tetrahedron 47, no. 23 (1991): 3773–78. http://dx.doi.org/10.1016/s0040-4020(01)80902-9.
Повний текст джерелаBenati, Luisa, Gianluca Calestani, Pier Carlo Montevecchi, and Piero Spagnolo. "Diazo transfer reaction of 2-(trimethylsilyl)-1,3-dithiane with tosyl azide. Reactivity of transient 2-diazo-1,3-dithiane." Journal of the Chemical Society, Chemical Communications, no. 19 (1995): 1999. http://dx.doi.org/10.1039/c39950001999.
Повний текст джерелаKuruba, Bharath Kumar, Nusrathulla Shariff, Samuel Vasanthkumar та Lourdusamy Emmanuvel. "ChemInform Abstract: NaOH/Et3N-Promoted Stereoselective One-Pot Synthesis of α-Diazo Oxime Ethers via Diazo Transfer Reaction." ChemInform 47, № 10 (лютий 2016): no. http://dx.doi.org/10.1002/chin.201610059.
Повний текст джерелаNagarajan, R., and L. Emmanuvel. "Unusual Cleavage of N-N Bond of 1-Arylamino-1,2,3-triazole Derivatives: A Simple and Alternate Approach to 4,5-Disubstituted-1H-1,2,3-triazoles." Asian Journal of Chemistry 31, no. 5 (March 28, 2019): 1057–61. http://dx.doi.org/10.14233/ajchem.2019.21857.
Повний текст джерелаBenati, Luisa, Gianluca Calestani, Daniele Nanni, Piero Spagnolo, and Marco Volta. "Diazo transfer reaction of 2-(trimethylsilyl)-1,3-dithiane with tosyl azide. Carbenic reactivity of transient 2-diazo-1,3-dithiane." Tetrahedron 53, no. 27 (July 1997): 9269–78. http://dx.doi.org/10.1016/s0040-4020(97)00538-3.
Повний текст джерелаZhmurov, Petr A., Dmitry V. Dar’in, Olga Yu Bakulina, and Mikhail Krasavin. "One-pot preparation of methyl 2-diazo-3-oxopropionates comprising an aqueous ‘sulfonyl-azide-free’ (SAFE) diazo transfer step." Mendeleev Communications 30, no. 3 (May 2020): 311–12. http://dx.doi.org/10.1016/j.mencom.2020.05.016.
Повний текст джерелаDamiano, Caterina, Paolo Sonzini, and Emma Gallo. "Iron catalysts with N-ligands for carbene transfer of diazo reagents." Chemical Society Reviews 49, no. 14 (2020): 4867–905. http://dx.doi.org/10.1039/d0cs00221f.
Повний текст джерелаBeletskaya, Irina P., та Igor D. Titanyuk. "Synthesis of α-Aryldiazophosphonates via a Diazo Transfer Reaction". Journal of Organic Chemistry 87, № 5 (22 лютого 2022): 2748–57. http://dx.doi.org/10.1021/acs.joc.1c02673.
Повний текст джерелаvan Dongen, Stijn F. M., Rosalie L. M. Teeuwen, Madhavan Nallani, Sander S. van Berkel, Jeroen J. L. M. Cornelissen, Roeland J. M. Nolte, and Jan C. M. van Hest. "Single-Step Azide Introduction in Proteins via an Aqueous Diazo Transfer." Bioconjugate Chemistry 20, no. 1 (January 21, 2009): 20–23. http://dx.doi.org/10.1021/bc8004304.
Повний текст джерелаLartia, Rémy, Pierre Murat, Pascal Dumy, and Eric Defrancq. "Versatile Introduction of Azido Moiety into Oligonucleotides through Diazo Transfer Reaction." Organic Letters 13, no. 20 (October 21, 2011): 5672–75. http://dx.doi.org/10.1021/ol202397e.
Повний текст джерелаKitamura, Mitsuru, Rie Sakata, Norifumi Tashiro, Azusa Ikegami, and Tatsuo Okauchi. "ChemInform Abstract: Synthesis of Diazonaphthoquinones from Naphthols by Diazo-Transfer Reaction." ChemInform 46, no. 45 (October 22, 2015): no. http://dx.doi.org/10.1002/chin.201545108.
Повний текст джерелаAlper, Phil B., Shang-Cheng Hung, and Chi-Huey Wong. "Metal catalyzed diazo transfer for the synthesis of azides from amines." Tetrahedron Letters 37, no. 34 (August 1996): 6029–32. http://dx.doi.org/10.1016/0040-4039(96)01307-x.
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