Artículos de revistas sobre el tema "3-acetals"
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Kassam, Karim, Paul C. Venneri y John Warkentin. "Reactions of alkoxyaryloxycarbenes with tethered triple bonds: a new synthesis of substituted benzofurans". Canadian Journal of Chemistry 75, n.º 9 (1 de septiembre de 1997): 1256–63. http://dx.doi.org/10.1139/v97-152.
Texto completoBuzatu, Alina Ramona, August E. Frissen, Lambertus A. M. van den Broek, Anamaria Todea, Marilena Motoc y Carmen Gabriela Boeriu. "Chemoenzymatic Synthesis of New Aromatic Esters of Mono- and Oligosaccharides". Processes 8, n.º 12 (11 de diciembre de 2020): 1638. http://dx.doi.org/10.3390/pr8121638.
Texto completode Carvalho, Leandro Lara, Robert Alan Burrow y Vera Lúcia Patrocinio Pereira. "Diastereoselective synthesis of nitroso acetals from (S,E)-γ-aminated nitroalkenes via multicomponent [4 + 2]/[3 + 2] cycloadditions promoted by LiCl or LiClO4". Beilstein Journal of Organic Chemistry 9 (30 de abril de 2013): 838–45. http://dx.doi.org/10.3762/bjoc.9.96.
Texto completoHlavatý, Jaromír y Miroslav Polášek. "Electrochemical Preparation of Alkynedial Tetramethyl Acetals". Collection of Czechoslovak Chemical Communications 73, n.º 1 (2008): 19–23. http://dx.doi.org/10.1135/cccc20080019.
Texto completoCollins, DJ, LM Downes y M. Kyriakou. "Enolic Ortho Esters. III. Preparation of a Keto Acetal by Hydride Reduction of an Enolic Ortho Ester". Australian Journal of Chemistry 42, n.º 9 (1989): 1617. http://dx.doi.org/10.1071/ch9891617.
Texto completoPashkovsky, F. S., D. I. Korneev y F. A. Lakhvich. "Transformations of 3,7-interphenylene 11-deoxyprostanoid formyl precursors in the acidic medium". Doklady of the National Academy of Sciences of Belarus 65, n.º 6 (26 de diciembre de 2021): 702–7. http://dx.doi.org/10.29235/1561-8323-2021-65-6-702-707.
Texto completoBlanáriková-Hlobilová, Iva, Lubor Fišera, Naďa Prónayová y Marian Koman. "1,3-Dipolar Cycloadditions of D-Erythrose- and D-Threose-Derived Alkenes with Nitrones". Collection of Czechoslovak Chemical Communications 68, n.º 5 (2003): 951–64. http://dx.doi.org/10.1135/cccc20030951.
Texto completoLopez, JC, AM Gomez y B. Fraserreid. "Cyclization Reactions of Tethered Radicals Derived From 4-O-Substituted α-D-erythro-Octa-2,6-dienopyranosides: Stereoselective Access to Carbocycles and Branched-Chain Sugars". Australian Journal of Chemistry 48, n.º 2 (1995): 333. http://dx.doi.org/10.1071/ch9950333.
Texto completoDenmark, Scott E., Vito Guagnano y Jean Vaugeois. "Studies on the reduction and hydrolysis of nitroso acetals". Canadian Journal of Chemistry 79, n.º 11 (1 de noviembre de 2001): 1606–16. http://dx.doi.org/10.1139/v01-132.
Texto completoYakovleva, Marina P. "Low-temperature reduction of acyclic carvomentholactone derivatives with diisobutylaluminum hydride in methylene chloride". Butlerov Communications 61, n.º 2 (29 de febrero de 2020): 24–28. http://dx.doi.org/10.37952/roi-jbc-01/20-61-2-24.
Texto completoPaquet, Jacques y Paul Brassard. "Reactions of polar dienes with o-quinones". Canadian Journal of Chemistry 67, n.º 8 (1 de agosto de 1989): 1354–58. http://dx.doi.org/10.1139/v89-207.
Texto completoDussault, Patrick H., Tony K. Trullinger y Su Cho-Shultz. "Chiral Silyl Ketene Acetals from Thioesters: Reaction with Acetals and Peroxyacetals to form 3-Alkoxy- and 3-Peroxyalkanoates". Tetrahedron 56, n.º 47 (noviembre de 2000): 9213–20. http://dx.doi.org/10.1016/s0040-4020(00)00894-2.
Texto completoKamitanaka, Tohru, Koji Morimoto, Toshifumi Dohi y Yasuyuki Kita. "Controlled-Coupling of Quinone Monoacetals by New Activation Methods: Regioselective Synthesis of Phenol-Derived Compounds". Synlett 30, n.º 10 (25 de marzo de 2019): 1125–43. http://dx.doi.org/10.1055/s-0037-1611735.
Texto completoVankar, Yashwant D., M. Venkatram Reddy y Narayan C. Chaudhuri. "Chiral acetals in organic synthesis: Regioselective synthesis of 2-and 3-hydroxy acetals from 2,3-olefinic acetals. Reinvestigation and further applications". Tetrahedron 50, n.º 37 (enero de 1994): 11057–78. http://dx.doi.org/10.1016/s0040-4020(01)85714-8.
Texto completoIsobe, Hiroyuki, Sota Sato, Takatsugu Tanaka, Hidetoshi Tokuyama y Eiichi Nakamura. "Thermal and Palladium-Catalyzed [3 + 2] Synthesis of Cyclopentadienone Acetals from Cyclopropenone Acetals and Acetylenes". Organic Letters 6, n.º 20 (septiembre de 2004): 3569–71. http://dx.doi.org/10.1021/ol0483450.
Texto completoDaia, G. Elena, Christopher D. Gabbutt, John D. Hepworth, B. Mark Heron, David E. Hibbs y Michael B. Hursthouse. "The directed lithiation of some 3-acylchromone acetals". Tetrahedron Letters 39, n.º 10 (marzo de 1998): 1215–18. http://dx.doi.org/10.1016/s0040-4039(97)10733-x.
Texto completoDussault, Patrick H., Tony K. Trullinger y Su Cho-Shultz. "ChemInform Abstract: Chiral Silyl Ketene Acetals from Thioesters: Reaction with Acetals and Peroxyacetals to Form 3-Alkoxy- and 3-Peroxyalkanoates." ChemInform 32, n.º 13 (27 de marzo de 2001): no. http://dx.doi.org/10.1002/chin.200113099.
Texto completoEvjen, Sigvart y Anne Fiksdahl. "Gold(I)-catalysed [3+3] cycloaddition of propargyl acetals and nitrones". Tetrahedron 72, n.º 23 (junio de 2016): 3270–76. http://dx.doi.org/10.1016/j.tet.2016.04.058.
Texto completoAhmed, Owais, Vandana Cherkadu, Praveen Kumar Kalavagunta y Jing Shang. "Solvent-dependent regio- and stereo-selective reactions of 3-formylchromones with 2-aminobenzothiazoles and transacetalization efficiency of the product 3-((benzo[d]thiazol-2-ylimino)butyl)-4H-chromen-4-one". RSC Advances 9, n.º 36 (2019): 20573–81. http://dx.doi.org/10.1039/c9ra02763g.
Texto completoDevendar, Ponnam, Arigari Niranjana Kumar, M. S. Bethu, Amtul Zehra, R. Pamanji, J. Venkateswara Rao, Ashok Kumar Tiwari, Balasubramanian Sridhar, K. V. N. Satya Srinivas y J. Kotesh Kumar. "Highly selective one pot synthesis and biological evaluation of novel 3-(allyloxy)-propylidene acetals of some natural terpenoids". RSC Advances 5, n.º 113 (2015): 93122–30. http://dx.doi.org/10.1039/c5ra18517c.
Texto completoSakai, Norio, Kazuki Sasaki, Hiroki Suzuki y Yohei Ogiwara. "One-Pot Synthesis of α-Halo β-Amino Acid Derivatives via the Difunctional Coupling of Ethyl α-Diazoacetate with Silyl Halides and N,O-Acetals or Aromatic Tertiary Amines". Synthesis 52, n.º 12 (23 de marzo de 2020): 1823–32. http://dx.doi.org/10.1055/s-0039-1690864.
Texto completoCrosby, Ian T., Geoffrey A. Pietersz y Justin A. Ripper. "Synthesis of Succinimidoalkylbenzaldehyde Analogues: Potential Bifunctional Linkers for Bioconjugation". Australian Journal of Chemistry 61, n.º 2 (2008): 138. http://dx.doi.org/10.1071/ch07404.
Texto completoKendall, Jackie D. y Paul D. Woodgate. "Towards the Diastereoselective Functionalization of Non-Racemic Acetal Derivatives of η6-Arylcarbonyl Complexes of Tricarbonylchromium". Australian Journal of Chemistry 51, n.º 12 (1998): 1083. http://dx.doi.org/10.1071/c98054.
Texto completoMotornov, Vladimir A., Andrey A. Tabolin, Roman A. Novikov, Yulia V. Nelyubina, Valentine G. Nenajdenko y Sema L. Ioffe. "Fluoronitroalkenes in tandem [4 + 1]/[3 + 2]-cycloaddition: one-pot three-component assembly of fluorinated bicyclic nitroso acetals". Organic Chemistry Frontiers 5, n.º 17 (2018): 2588–94. http://dx.doi.org/10.1039/c8qo00623g.
Texto completoSaget, Raphaël, Piotr Jaunky y Elisabet Duñach. "Bi(OTf)3-catalysed intramolecular cyclisation of unsaturated acetals". RSC Advances 11, n.º 34 (2021): 21066–72. http://dx.doi.org/10.1039/d1ra03686f.
Texto completoVankar, Yashwant D. y Anita Bawa. "A Simple Synthesis of 3-Nitrocycloalkenones and their Acetals". Synthetic Communications 15, n.º 14 (diciembre de 1985): 1253–56. http://dx.doi.org/10.1080/00397918508077273.
Texto completoLYUBCHANSKAYA, V. M. y V. G. GRANIK. "ChemInform Abstract: Lactam Acetals and Acid Amide Acetals. Part 58. Novel Synthesis of 3- Nitro-5-hydroxybenzofurans." ChemInform 22, n.º 5 (23 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199105191.
Texto completoAntonova, Yulia A., Yulia V. Nelyubina, Sema L. Ioffe y Andrey A. Tabolin. "[3+3]-Annulation of Cyclic Nitronates with Vinyl Diazoacetates: Diastereoselective Synthesis of Partially Saturated [1,2]Oxazino[2,3-b][1,2]oxazines and Their Base-Promoted Ring Contraction to Pyrrolo[1,2-b][1,2]oxazine Derivatives". Molecules 28, n.º 7 (28 de marzo de 2023): 3025. http://dx.doi.org/10.3390/molecules28073025.
Texto completoSchiavo, Lucie, Loïc Jeanmart, Steve Lanners, Sabine Choppin y Gilles Hanquet. "FeCl3·6H2O/acetaldehyde, a versatile system for the deprotection of ketals and acetals via a transacetalization process". New Journal of Chemistry 41, n.º 4 (2017): 1421–24. http://dx.doi.org/10.1039/c6nj03439j.
Texto completoRadulović, Niko S. y Milan S. Nešić. "Diverse acetals from stoichiometric amounts of aldehydes and alcohols under very mild conditions: a new twist to PPh3–CCl4 reagent combination". RSC Advances 6, n.º 95 (2016): 93068–80. http://dx.doi.org/10.1039/c6ra19980a.
Texto completoNavarro, Cristina, Nathan D. Shapiro, Maurizio Bernasconi, Takahiro Horibe y F. Dean Toste. "Gold(I)-catalyzed enantioselective [3+2] and [3+3] cycloaddition reactions of propargyl acetals/ketals". Tetrahedron 71, n.º 35 (septiembre de 2015): 5800–5805. http://dx.doi.org/10.1016/j.tet.2015.04.109.
Texto completoKim, Sunggak, Joo Hyeon Park y Joo Moon Lee. "Facile preparation of α,β-unsaturated O,S-acetals and mixed acetals via 3-alkoxy-2-alkenylenesulfonium salts." Tetrahedron Letters 34, n.º 36 (septiembre de 1993): 5769–72. http://dx.doi.org/10.1016/s0040-4039(00)73856-1.
Texto completoSrivastava, Abhijeet, Gaurav Shukla, Anugula Nagaraju, Girijesh Kumar Verma, Keshav Raghuvanshi, Raymond C. F. Jones y Maya Shankar Singh. "In(OTf)3-catalysed one-pot versatile pyrrole synthesis through domino annulation of α-oxoketene-N,S-acetals with nitroolefins". Org. Biomol. Chem. 12, n.º 29 (2014): 5484–91. http://dx.doi.org/10.1039/c4ob00781f.
Texto completoGasparski, Catherine M., Paul M. Herrinton, Larry E. Overman y John P. Wolfe. "Synthesis of 3-acyltetrahydrofurans from formaldehyde acetals of allylic diols". Tetrahedron Letters 41, n.º 49 (diciembre de 2000): 9431–35. http://dx.doi.org/10.1016/s0040-4039(00)01571-9.
Texto completoKomeyama, Kimihiro, Ryoichi Igawa, Takayuki Morimoto y Ken Takaki. "Catalytic Cyclization of AlkenylN,O-Acetals by Fe(OTf)3". Chemistry Letters 38, n.º 7 (5 de julio de 2009): 724–25. http://dx.doi.org/10.1246/cl.2009.724.
Texto completoDAIA, G. E., C. D. GABBUTT, J. D. HEPWORTH, B. M. HERON, D. E. HIBBS y M. B. HURSTHOUSE. "ChemInform Abstract: The Directed Lithiation of Some 3-Acylchromone Acetals." ChemInform 29, n.º 21 (22 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199821125.
Texto completoGuss, L. T., L. V. Ershov, G. A. Bogdanova y V. G. Granik. "Acetals of lactams and acid amides 55. Study of reaction of 3-oxopyridine and isoquinolin-3-one derivatives with dimethylformamide diethyl acetal". Chemistry of Heterocyclic Compounds 26, n.º 2 (febrero de 1990): 183–88. http://dx.doi.org/10.1007/bf00499413.
Texto completoCambie, RC, SE Holroyd, PS Rutledge y PD Woodgate. "Experiments Directed Towards the Synthesis of Anthracyclinones. XVII. Cyclization Reactions of Some Anthraquinone Conduritol Acetals". Australian Journal of Chemistry 46, n.º 1 (1993): 37. http://dx.doi.org/10.1071/ch9930037.
Texto completoLiu, Yi-Wen, Rui-Jun Ma, Jia-Hang Yan, Zhu Zhou y Bang-Guo Wei. "Asymmetric synthesis of (−)-sedacryptine through a diastereoselective Mannich reaction of N,O-acetals with ketones". Organic & Biomolecular Chemistry 16, n.º 5 (2018): 771–79. http://dx.doi.org/10.1039/c7ob02989f.
Texto completoSomogyi, László. "Synthesis, oxidation and dehydrogenation of cyclicN,O- andN,S-Acetals. II . Transformation ofN,S-acetals: 3-Acylbenzothiazolines and -thiazolidines". Journal of Heterocyclic Chemistry 43, n.º 5 (septiembre de 2006): 1141–50. http://dx.doi.org/10.1002/jhet.5570430502.
Texto completoLöwe, Christiane, Gottfried Huttner, Laszlo Zsolnai y Heinz Berke. "Acetalisierte Formylmangan-Komplexe / Acetals of Formyl Manganese Complexes". Zeitschrift für Naturforschung B 43, n.º 1 (1 de enero de 1988): 25–30. http://dx.doi.org/10.1515/znb-1988-0106.
Texto completoMöhrle, Hans y Heinz Dwuletzki. "Lactamacetale als potentielle Enamin-Synthone in Heterocyclensynthesen, 4. Mitteilung Einstufen-Synthese des γ-Carbolingerüsts durch Diels-Alder-Reaktion von Indol-„Keten-N,O-acetalen“/ Lactam Acetals as Potential Enamine Synthons in Heterocyclic Synthesis, 4th Communication. One Step Synthesis of the γ-Carboline Frame via Diels-Alder Reaction of Indol-“Ketene-N.O-Acetals”". Zeitschrift für Naturforschung B 42, n.º 8 (1 de agosto de 1987): 1032–34. http://dx.doi.org/10.1515/znb-1987-0818.
Texto completoVANKAR, Y. D., M. V. REDDY y N. C. CHAUDHURI. "ChemInform Abstract: Asymmetric Synthesis. Part 2. Chiral Acetals in Organic Synthesis: Regioselective Synthesis of 2- and 3-Hydroxy Acetals from 2,3-Olefinic Acetals. Reinvestigation and Further Applications." ChemInform 26, n.º 8 (18 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199508076.
Texto completoXiao, Tiebo, Ping Zhang, Yang Xie, Jun Wang y Lei Zhou. "CuI-catalyzed cross-coupling of terminal alkynes with dialkoxycarbenes: a general method for the synthesis of unsymmetrical propargylic acetals". Org. Biomol. Chem. 12, n.º 32 (2014): 6215–22. http://dx.doi.org/10.1039/c4ob00614c.
Texto completoDussault, P. H., R. J. Lee, J. A. Schultz y Y. S. Suh. "Reaction of peroxyacetals with silyl ketene acetals: synthesis of 3-peroxyalkanoates and 3-peroxyalkanals". Tetrahedron Letters 41, n.º 29 (julio de 2000): 5457–60. http://dx.doi.org/10.1016/s0040-4039(00)00914-x.
Texto completoGupta, Akhilesh K., R. T. Chakrasali, H. Ila y H. Junjappa. "Reaction of Polarized KeteneS,N-Acetals with Bromoacetaldehyde Diethyl Acetal: Synthesis of 1-Substituted 3-Acyl- and 3-Nitro-2-methylthiopyrroles and 1,2-Annulated 3-Acylpyrroles". Synthesis 1989, n.º 02 (1989): 141–42. http://dx.doi.org/10.1055/s-1989-27179.
Texto completoCao, Zhicheng, Xin Deng, Chao Chen, Yonghong Liu, Lei Yu y Xuefeng Jiang. "Synergetic catalysis of Se and Cu allowing diethoxylation of halomethylene ketones using O2 as the mild oxidant". Reaction Chemistry & Engineering 6, n.º 3 (2021): 454–58. http://dx.doi.org/10.1039/d0re00471e.
Texto completoLyu, Longyun, Ming Yu Jin, Qijie He, Han Xie, Zhaoxiang Bian y Jun Wang. "Bi(OTf)3-catalyzed addition of isocyanides to 2H-chromene acetals: an efficient pathway for accessing 2-carboxamide-2H-chromenes". Organic & Biomolecular Chemistry 14, n.º 34 (2016): 8088–91. http://dx.doi.org/10.1039/c6ob01355d.
Texto completoKIM, S., J. H. PARK y J. M. LEE. "ChemInform Abstract: Facile Preparation of α,β-Unsaturated O,S-Acetals and Mixed Acetals via 3-Alkoxy-2-alkenylenesulfonium Salts." ChemInform 24, n.º 48 (20 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199348107.
Texto completoHuang, Yong Kui, Li Yu, Guo Bin Duan, Yun Zhi Wang, Ming Bo Xu y Shui Jin Yang. "Catalytic Application of H3PW6Mo6O40/SiO2 in Synthesis of Acetals and Ketals". Advanced Materials Research 531 (junio de 2012): 304–7. http://dx.doi.org/10.4028/www.scientific.net/amr.531.304.
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