Academic literature on the topic 'Oxazines and substituted aldehydes'

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Journal articles on the topic "Oxazines and substituted aldehydes"

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D.T., Biradar, and M. B. Swami Dr. "Synthesis of Schiff's Bases from 2-Amino-4H-1, 3-Oxazine / Thiazine and Substituted Aldehydes and their Transition Metal Complexes." International Journal of Current Science Research and Review 04, no. 07 (2021): 677–83. https://doi.org/10.47191/ijcsrr/V4-i7-09.

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Abstract : Objective: Many methods can be found in literature for the synthesis a Oxazines and Thiazines. Few are reported for one-pot multi component cyclo-condensation of an alkayane urea / Thiourea and Aldehyde to 2- amino-4H-1, 3-Oxazines or Thiazines. Different catalysts are reported like Trifluoro-acetic acid, glacial acetic acid under reflux condition Mandal and Co-workers have utilized perchloric acid (HClO4) supported on silica gel as catalyst under solvent free condition ytterbium trifluorate [Yb(OTF)3] plays role of Lewis acid. It is also used in several Diel’s-Alder cyclo-add
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Sheng, Jinyu, Xiang Su, Chengyao Cao, and Chao Chen. "Synthesis of benzo[1,3]oxazines via copper(i)-catalyzed cascade annulation of nitriles, aldehydes and diaryliodonium salts." Organic Chemistry Frontiers 3, no. 4 (2016): 501–4. http://dx.doi.org/10.1039/c6qo00012f.

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A copper(i)-catalyzed one-pot [2 + 2 + 2] cascade annulation reaction of diaryliodoniums, nitriles, and aldehydes has been developed for the efficient synthesis of 2,4-substituted benzoxazine derivatives.
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Háznagy, Márton Benedek, Antal Csámpai, Imre Ugrai, Barnabás Molnár, Matti Haukka, and Zsolt Szakonyi. "Stereoselective Synthesis and Catalytical Application of Perillaldehyde-Based 3-Amino-1,2-diol Regioisomers." International Journal of Molecular Sciences 25, no. 8 (2024): 4325. http://dx.doi.org/10.3390/ijms25084325.

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A library of regioisomeric monoterpene-based aminodiols was synthesised and applied as chiral catalysts in the addition of diethylzinc to benzaldehyde. The synthesis of the first type of aminodiols was achieved starting from (−)-8,9-dihydroperillaldehyde via reductive amination, followed by Boc protection and dihydroxylation with the OsO4/NMO system. Separation of formed stereoisomers resulted in a library of aminodiol diastereoisomers. The library of regioisomeric analogues was obtained starting from (−)-8,9-dihydroperillic alcohol, which was transformed into a mixture of allylic trichloroace
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Karade, Nandkishor, Girdharilal Tiwari, and Sumit Gampawar. "Efficient Oxidative Conversion of Aldehydes to 2-Substituted Oxazolines and Oxazines Using (Diacetoxyiodo)benzene." Synlett 2007, no. 12 (2007): 1921–24. http://dx.doi.org/10.1055/s-2007-982571.

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Devi, Kalpana, and Monica Kachroo. "Synthesis and Docking Studies of Oxazine Derivatives as Anti-inflammatory and Antioxidant Agents." DER PHARMA CHEMICA 13, no. 3 (2021): 9. https://doi.org/10.5281/zenodo.11070994.

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A new series of N-(4-{4-(substituted phenyl)-2-[(4-fluro-benzylidene)-amino]-6H-[1,3] oxazine-6-yl}-phenyl)-isonicotiamide were synthesized by reaction of p-amino acetophenone with isonicotinyl chloride to obtain the secondary amides. ClaisenSchmidth condensation reaction with substituted aldehydes led to the formation of corresponding chalcones. These chalcones were cyclized with urea to form oxazine which further reacted with p-fluorobenzaldehyde to form the corresponding Schiff’s bases. All the synthesized compounds were characterized by IR and 1HNMR spectral data, mass spectra and el
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Devi, Kalpana, and Monica Kachroo. "Synthesis and Docking Studies of Oxazine Derivatives as Anti-inflammatory and Antioxidant Agents." Der Pharma Chemica 13, no. 3 (2021): 9. https://doi.org/10.5281/zenodo.14722735.

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A new series of N-(4-{4-(substituted phenyl)-2-[(4-fluro-benzylidene)-amino]-6H-[1,3] oxazine-6-yl}-phenyl)-isonicotiamide were synthesized by reaction of p-amino acetophenone with isonicotinyl chloride to obtain the secondary amides. ClaisenSchmidth condensation reaction with substituted aldehydes led to the formation of corresponding chalcones. These chalcones were cyclized with urea to form oxazine which further reacted with p-fluorobenzaldehyde to form the corresponding Schiff’s bases. All the synthesized compounds were characterized by IR and 1HNMR spectral data, mass spectra and el
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Yasui, Yusuke, Kento Ogata, Itaru Sato та Yujiro Hayashi. "Asymmetric Aldol Reaction of α-Acetoxyimino Aldehydes and its Application in the Synthesis of Substituted 1,2-Oxazine Derivatives". Advanced Synthesis & Catalysis 356, № 14-15 (2014): 3106–18. http://dx.doi.org/10.1002/adsc.201400294.

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Yasui, Yusuke, Kento Ogata, Itaru Sato та Yujiro Hayashi. "ChemInform Abstract: Asymmetric Aldol Reaction of α-Acetoxyimino Aldehydes and Its Application in the Synthesis of Substituted 1,2-Oxazine Derivatives." ChemInform 46, № 13 (2015): no. http://dx.doi.org/10.1002/chin.201513253.

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Peter, Clovis, Philippe Geoffroy, and Michel Miesch. "Highly diastereoselective access to polyfunctionalized 1,3-oxazines promoted by Brønsted/Lewis acids." Organic Chemistry Frontiers 5, no. 4 (2018): 566–70. http://dx.doi.org/10.1039/c7qo00891k.

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The Brønsted/Lewis acid catalyzed reaction of α-alkyloxyamides tethered to α,β-unsaturated ketones (aldehydes) afforded exclusively polyfunctionalized 1,3-oxazines with high diastereoselectivities and in high yields.
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Belz, Tyson, Saleh Ihmaid, Jasim Al-Rawi, and Steve Petrovski. "Synthesis Characterization and Antibacterial, Antifungal Activity of N-(Benzyl Carbamoyl or Carbamothioyl)-2-hydroxy Substituted Benzamide and 2-Benzyl Amino-Substituted Benzoxazines." International Journal of Medicinal Chemistry 2013 (October 31, 2013): 1–20. http://dx.doi.org/10.1155/2013/436397.

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New N-(benzyl carbamothioyl)-2-hydroxy substituted benzamides 13, 20, and 21 were synthesized using sodium bicarbonate and benzyl amine with 2-thioxo-substituted-1,3-benzoxazines 6, 10a, b, 11c, and 12a–n. The 2-thioxo-substituted-1,3-oxazines 6, 10a-b, 11d 12a–n, and 26 were converted to the corresponding 2-methylthio-substituted-1,3-oxazines 14a–l and 24 which were then converted to 2-benzyl amino-substituted-benzoxazines 15a–i by refluxing with benzylamine. Products 15a, b, e, f, and g were also synthesized by boiling the corresponding N-(benzyl carbamothioyl)-2-hydroxy substituted benzamid
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Dissertations / Theses on the topic "Oxazines and substituted aldehydes"

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Pinar, Ayse Nur. "Reaction Of Propargyl Aldehydes With Hydrazinium Salts: Synthesis Of Ferrocenyl And Phenyl Substituted Pyrazoles." Master's thesis, METU, 2008. http://etd.lib.metu.edu.tr/upload/3/12609769/index.pdf.

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Pyrazoles have been focus of a large number of investigations in the design and synthesis of novel biologically active agents that show remarkable medicinal activities. Although pyrazoles have been studied for over a century as an important class of heterocyclic compounds, they still continue to attract considerable attention due to the wide range of medicinal activities they possess. Recent studies have shown that combination of a ferrocenyl unit with structural features of pyrazoles can lead to products with enhanced or/and unexpected biological activity since several ferrocene derivatives h
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Walts, Alan Edmund. "I. Total Synthesis of (-)-ptilocaulin. II. Stereoselective reactions of allylboronic esters with substituted aldehydes." Thesis, Massachusetts Institute of Technology, 1985. http://hdl.handle.net/1721.1/15290.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 1985.<br>MICROFICHE COPY AVAILABLE IN ARCHIVES AND SCIENCE.<br>Vita.<br>Includes bibliographical references.<br>by Alan Edmund Walts.<br>Ph.D.
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Ramos, Ferronatto Gabriel. "Dynamic resolution of alpha-substituted dihydrocinnamic aldehydes. A new asymmetric synthesis of pharmaceutically important amine building blocks." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2013. http://amslaurea.unibo.it/6081/.

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Crystallization-induced diastereoisomer transformation (CIDT) was successfully employed in the enantioselective synthesis of 2-alkyl-3-aryl-propan-1-amines. These products are seen as potentially useful building blocks in the field of asymmetric organic chemistry, notably for pharmaceutically relevant compounds. The procedure was based on a recently reported protocol for deracemization of dihydrocinnamic aldehydes in which enantiomerically enriched 1-(amino(phenyl)methyl)naphthalen-2-ol (Betti base) is employed as a resolving agent. Additionally, fenpropimorph, a biologically active substance
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Stanfield, Charles Freeman. "Synthesis of alpha-amino aldehydes as kallikrein inhibitors; synthetic methods for preparation of beta-substituted cysteine analogues." Diss., The University of Arizona, 1989. http://hdl.handle.net/10150/184738.

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The first half of this dissertation describes the synthesis and biological activities of a series of amino aldehydes; which were derivatives of the basic amino acids, arginine, lysine and ornithine. The synthesis of the amino aldehydes was complicated by the difficulty of producing an intermediate oxidation state (the aldehyde) in the presence of two other functional groups (the α-amino, and the side chain functionality). The amino aldehydes were of biological interest due to the fact that they were inhibitors of the proteolytic enzymes called kallikreins. The kallikreins are known to be invol
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Pernik, Indrek. "Exploring small bite-angle PNP and PCP ligands for the rhodium-catalysed intermolecular hydroacylation of b-s-substituted aldehydes with alkenes and alkynes." Thesis, University of Oxford, 2014. http://ora.ox.ac.uk/objects/uuid:aaf41dc2-1147-44f4-b609-5bf7ada1b060.

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This thesis discusses the intermolecular hydroacylation reaction using cationic rhodium bis- phosphine complexes as catalysts. A series of small bite-angle rhodium bis-phosphine complexes have been prepared and characterised. The reactivity of these complexes has been investigated in order to gather information about the effect of subtle changes in the ligand design and they are compared to the previously reported catalysts. Chapter 2 presents the challenges involved in the synthesis of small bite-angle isopropyl and cyclohexyl PNP and PCP bis-phosphine ligand containing rhodium complexes. The
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CHEN, JUNG-HSUAN, and 陳蓉萱. "1. An Efficient and Convenient Synthesis of Fully-Substituted 1,2,3-Triazole 2.Organocatalytic Domino Michael /Hemiacetalization of beta-Tetralone and alpha,beta-Unsaturated Aldehydes 3. Total Synthesis of (±)-Viroallosecurinine." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/89468652340197012528.

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博士<br>國立臺灣師範大學<br>化學系<br>100<br>There are three parts of research topics in this thesis. The first topic is an alternative and direct access to fully-substituted 1,2,3-triazoles. Treatment of diazo compound with 4-methoxyaniline derived aryl imines in the presence of DBU provided ethyl 1-(4-methoxyphenyl)-5-phenyl-1H-1,2,3-triazole-4-carboxylate in good to high yields. A reasonable mechanism is proposed that involves the addition of an imine nitrogen atom to the terminal nitrogen atom of the diazo compound, followed by aromatization to give the 1,2,3-triazole. The presence of the 4-carboxy gro
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Strotman, Neil Adham. "I. Stereochemistry of cyclopropane formation involving group (IV) organometallic complexes : II. Slower stoichiometric and faster catalytic reduction of aldehydes by the PPh₃ substituted hydroxycyclopentadienyl ruthenium hydride [2,5-Ph₂-3,4-Tol₂([eta]⁵-C₄COH)]Ru(CO)(PPh₃)H: a highly complex chemoselective catalyst for hydrogenation of aldehydes over ketones /." 2005. http://catalog.hathitrust.org/api/volumes/oclc/70792586.html.

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Books on the topic "Oxazines and substituted aldehydes"

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Kulmala, Aija. Formation of fused-ring 1,3/3,1-oxazines and hydrolytic decomposition of 2-substituted oxazolidines and tetrahydro-1,3-oxazines: The simplest models for glycosylamines. A. Kulmala, 1991.

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Calvert, Jack, Abdelwahid Mellouki, John Orlando, Michael Pilling, and Timothy Wallington. Mechanisms of Atmospheric Oxidation of the Oxygenates. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199767076.001.0001.

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Prepared by an international team of eminent atmospheric scientists, Mechanisms of Atmospheric Oxidation of the Oxygenates is an authoritative source of information on the role of oxygenates in the chemistry of the atmosphere. The oxygenates, including the many different alcohols, ethers, aldehydes, ketones, acids, esters, and nitrogen-atom containing oxygenates, are of special interest today due to their increased use as alternative fuels and fuel additives. This book describes the physical properties of oxygenates, as well as the chemical and photochemical parameters that determine their rea
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Book chapters on the topic "Oxazines and substituted aldehydes"

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JEDLIŃSKI, Z. J., M. BERO, J. KASPERCZYK, and M. KOWALCZUK. "Polymerization of Substituted Oxiranes, Epoxy Aldehydes, and Derived Oxacyclic Monomers." In ACS Symposium Series. American Chemical Society, 1985. http://dx.doi.org/10.1021/bk-1985-0286.ch016.

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HATADA, K., T. KITAYAMA, Y. OKAMOTO, et al. "Polymers of α-Substituted Benzyl Methacrylates and Aliphatic Aldehydes as New Types of Electron-Beam Resists." In ACS Symposium Series. American Chemical Society, 1985. http://dx.doi.org/10.1021/bk-1984-0266.ch020.

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Göttlich, R. "Heteroatom-Substituted Allyl Anions." In Aldehydes. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-025-00262.

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Lindenschmidt, A. "3-Silicon-Substituted Aldehydes." In Aldehydes. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-025-00586.

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Lindenschmidt, A. "3-Tin-Substituted Aldehydes." In Aldehydes. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-025-00588.

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Lindenschmidt, A. "3-Boron-Substituted Aldehydes." In Aldehydes. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-025-00590.

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Lindenschmidt, A. "3-Halogen-Substituted Aldehydes." In Aldehydes. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-025-00592.

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Lindenschmidt, A. "3-Oxygen-Substituted Aldehydes." In Aldehydes. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-025-00594.

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Lindenschmidt, A. "3-Sulfur-Substituted Aldehydes." In Aldehydes. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-025-00606.

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Lindenschmidt, A. "3-Nitrogen-Substituted Aldehydes." In Aldehydes. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-025-00608.

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Conference papers on the topic "Oxazines and substituted aldehydes"

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Ito, Hiroshi, Klaas Schildknegt, and Eugene A. Mash. "Negative chemical amplification resist systems based on polyhydroxystyrenes and N-substituted imides or aldehydes." In Advances in Resist Technology and Processing VIII, edited by Hiroshi Ito. SPIE, 1991. http://dx.doi.org/10.1117/12.46389.

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