Статті в журналах з теми "3-acetals"
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Kassam, Karim, Paul C. Venneri, and John Warkentin. "Reactions of alkoxyaryloxycarbenes with tethered triple bonds: a new synthesis of substituted benzofurans." Canadian Journal of Chemistry 75, no. 9 (September 1, 1997): 1256–63. http://dx.doi.org/10.1139/v97-152.
Повний текст джерелаBuzatu, Alina Ramona, August E. Frissen, Lambertus A. M. van den Broek, Anamaria Todea, Marilena Motoc, and Carmen Gabriela Boeriu. "Chemoenzymatic Synthesis of New Aromatic Esters of Mono- and Oligosaccharides." Processes 8, no. 12 (December 11, 2020): 1638. http://dx.doi.org/10.3390/pr8121638.
Повний текст джерелаde Carvalho, Leandro Lara, Robert Alan Burrow та 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 квітня 2013): 838–45. http://dx.doi.org/10.3762/bjoc.9.96.
Повний текст джерелаHlavatý, Jaromír, and Miroslav Polášek. "Electrochemical Preparation of Alkynedial Tetramethyl Acetals." Collection of Czechoslovak Chemical Communications 73, no. 1 (2008): 19–23. http://dx.doi.org/10.1135/cccc20080019.
Повний текст джерелаCollins, DJ, LM Downes, and M. Kyriakou. "Enolic Ortho Esters. III. Preparation of a Keto Acetal by Hydride Reduction of an Enolic Ortho Ester." Australian Journal of Chemistry 42, no. 9 (1989): 1617. http://dx.doi.org/10.1071/ch9891617.
Повний текст джерелаPashkovsky, F. S., D. I. Korneev, and 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, no. 6 (December 26, 2021): 702–7. http://dx.doi.org/10.29235/1561-8323-2021-65-6-702-707.
Повний текст джерелаBlanáriková-Hlobilová, Iva, Lubor Fišera, Naďa Prónayová, and Marian Koman. "1,3-Dipolar Cycloadditions of D-Erythrose- and D-Threose-Derived Alkenes with Nitrones." Collection of Czechoslovak Chemical Communications 68, no. 5 (2003): 951–64. http://dx.doi.org/10.1135/cccc20030951.
Повний текст джерелаLopez, JC, AM Gomez та 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, № 2 (1995): 333. http://dx.doi.org/10.1071/ch9950333.
Повний текст джерелаDenmark, Scott E., Vito Guagnano, and Jean Vaugeois. "Studies on the reduction and hydrolysis of nitroso acetals." Canadian Journal of Chemistry 79, no. 11 (November 1, 2001): 1606–16. http://dx.doi.org/10.1139/v01-132.
Повний текст джерелаYakovleva, Marina P. "Low-temperature reduction of acyclic carvomentholactone derivatives with diisobutylaluminum hydride in methylene chloride." Butlerov Communications 61, no. 2 (February 29, 2020): 24–28. http://dx.doi.org/10.37952/roi-jbc-01/20-61-2-24.
Повний текст джерелаPaquet, Jacques, and Paul Brassard. "Reactions of polar dienes with o-quinones." Canadian Journal of Chemistry 67, no. 8 (August 1, 1989): 1354–58. http://dx.doi.org/10.1139/v89-207.
Повний текст джерелаDussault, Patrick H., Tony K. Trullinger, and Su Cho-Shultz. "Chiral Silyl Ketene Acetals from Thioesters: Reaction with Acetals and Peroxyacetals to form 3-Alkoxy- and 3-Peroxyalkanoates." Tetrahedron 56, no. 47 (November 2000): 9213–20. http://dx.doi.org/10.1016/s0040-4020(00)00894-2.
Повний текст джерелаKamitanaka, Tohru, Koji Morimoto, Toshifumi Dohi, and Yasuyuki Kita. "Controlled-Coupling of Quinone Monoacetals by New Activation Methods: Regioselective Synthesis of Phenol-Derived Compounds." Synlett 30, no. 10 (March 25, 2019): 1125–43. http://dx.doi.org/10.1055/s-0037-1611735.
Повний текст джерелаVankar, Yashwant D., M. Venkatram Reddy, and 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, no. 37 (January 1994): 11057–78. http://dx.doi.org/10.1016/s0040-4020(01)85714-8.
Повний текст джерелаIsobe, Hiroyuki, Sota Sato, Takatsugu Tanaka, Hidetoshi Tokuyama, and Eiichi Nakamura. "Thermal and Palladium-Catalyzed [3 + 2] Synthesis of Cyclopentadienone Acetals from Cyclopropenone Acetals and Acetylenes." Organic Letters 6, no. 20 (September 2004): 3569–71. http://dx.doi.org/10.1021/ol0483450.
Повний текст джерелаDaia, G. Elena, Christopher D. Gabbutt, John D. Hepworth, B. Mark Heron, David E. Hibbs, and Michael B. Hursthouse. "The directed lithiation of some 3-acylchromone acetals." Tetrahedron Letters 39, no. 10 (March 1998): 1215–18. http://dx.doi.org/10.1016/s0040-4039(97)10733-x.
Повний текст джерелаDussault, Patrick H., Tony K. Trullinger, and 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, no. 13 (March 27, 2001): no. http://dx.doi.org/10.1002/chin.200113099.
Повний текст джерелаEvjen, Sigvart, and Anne Fiksdahl. "Gold(I)-catalysed [3+3] cycloaddition of propargyl acetals and nitrones." Tetrahedron 72, no. 23 (June 2016): 3270–76. http://dx.doi.org/10.1016/j.tet.2016.04.058.
Повний текст джерелаAhmed, Owais, Vandana Cherkadu, Praveen Kumar Kalavagunta, and 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, no. 36 (2019): 20573–81. http://dx.doi.org/10.1039/c9ra02763g.
Повний текст джерелаDevendar, Ponnam, Arigari Niranjana Kumar, M. S. Bethu, Amtul Zehra, R. Pamanji, J. Venkateswara Rao, Ashok Kumar Tiwari, Balasubramanian Sridhar, K. V. N. Satya Srinivas, and J. Kotesh Kumar. "Highly selective one pot synthesis and biological evaluation of novel 3-(allyloxy)-propylidene acetals of some natural terpenoids." RSC Advances 5, no. 113 (2015): 93122–30. http://dx.doi.org/10.1039/c5ra18517c.
Повний текст джерелаSakai, Norio, Kazuki Sasaki, Hiroki Suzuki та 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, № 12 (23 березня 2020): 1823–32. http://dx.doi.org/10.1055/s-0039-1690864.
Повний текст джерелаCrosby, Ian T., Geoffrey A. Pietersz, and Justin A. Ripper. "Synthesis of Succinimidoalkylbenzaldehyde Analogues: Potential Bifunctional Linkers for Bioconjugation." Australian Journal of Chemistry 61, no. 2 (2008): 138. http://dx.doi.org/10.1071/ch07404.
Повний текст джерелаKendall, Jackie D., and Paul D. Woodgate. "Towards the Diastereoselective Functionalization of Non-Racemic Acetal Derivatives of η6-Arylcarbonyl Complexes of Tricarbonylchromium." Australian Journal of Chemistry 51, no. 12 (1998): 1083. http://dx.doi.org/10.1071/c98054.
Повний текст джерелаMotornov, Vladimir A., Andrey A. Tabolin, Roman A. Novikov, Yulia V. Nelyubina, Valentine G. Nenajdenko, and 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, no. 17 (2018): 2588–94. http://dx.doi.org/10.1039/c8qo00623g.
Повний текст джерелаSaget, Raphaël, Piotr Jaunky, and Elisabet Duñach. "Bi(OTf)3-catalysed intramolecular cyclisation of unsaturated acetals." RSC Advances 11, no. 34 (2021): 21066–72. http://dx.doi.org/10.1039/d1ra03686f.
Повний текст джерелаVankar, Yashwant D., and Anita Bawa. "A Simple Synthesis of 3-Nitrocycloalkenones and their Acetals." Synthetic Communications 15, no. 14 (December 1985): 1253–56. http://dx.doi.org/10.1080/00397918508077273.
Повний текст джерелаLYUBCHANSKAYA, V. M., and V. G. GRANIK. "ChemInform Abstract: Lactam Acetals and Acid Amide Acetals. Part 58. Novel Synthesis of 3- Nitro-5-hydroxybenzofurans." ChemInform 22, no. 5 (August 23, 2010): no. http://dx.doi.org/10.1002/chin.199105191.
Повний текст джерелаAntonova, Yulia A., Yulia V. Nelyubina, Sema L. Ioffe, and 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, no. 7 (March 28, 2023): 3025. http://dx.doi.org/10.3390/molecules28073025.
Повний текст джерелаSchiavo, Lucie, Loïc Jeanmart, Steve Lanners, Sabine Choppin, and Gilles Hanquet. "FeCl3·6H2O/acetaldehyde, a versatile system for the deprotection of ketals and acetals via a transacetalization process." New Journal of Chemistry 41, no. 4 (2017): 1421–24. http://dx.doi.org/10.1039/c6nj03439j.
Повний текст джерелаRadulović, Niko S., and 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, no. 95 (2016): 93068–80. http://dx.doi.org/10.1039/c6ra19980a.
Повний текст джерелаNavarro, Cristina, Nathan D. Shapiro, Maurizio Bernasconi, Takahiro Horibe, and F. Dean Toste. "Gold(I)-catalyzed enantioselective [3+2] and [3+3] cycloaddition reactions of propargyl acetals/ketals." Tetrahedron 71, no. 35 (September 2015): 5800–5805. http://dx.doi.org/10.1016/j.tet.2015.04.109.
Повний текст джерелаKim, Sunggak, Joo Hyeon Park та Joo Moon Lee. "Facile preparation of α,β-unsaturated O,S-acetals and mixed acetals via 3-alkoxy-2-alkenylenesulfonium salts." Tetrahedron Letters 34, № 36 (вересень 1993): 5769–72. http://dx.doi.org/10.1016/s0040-4039(00)73856-1.
Повний текст джерелаSrivastava, Abhijeet, Gaurav Shukla, Anugula Nagaraju, Girijesh Kumar Verma, Keshav Raghuvanshi, Raymond C. F. Jones та 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, № 29 (2014): 5484–91. http://dx.doi.org/10.1039/c4ob00781f.
Повний текст джерелаGasparski, Catherine M., Paul M. Herrinton, Larry E. Overman, and John P. Wolfe. "Synthesis of 3-acyltetrahydrofurans from formaldehyde acetals of allylic diols." Tetrahedron Letters 41, no. 49 (December 2000): 9431–35. http://dx.doi.org/10.1016/s0040-4039(00)01571-9.
Повний текст джерелаKomeyama, Kimihiro, Ryoichi Igawa, Takayuki Morimoto, and Ken Takaki. "Catalytic Cyclization of AlkenylN,O-Acetals by Fe(OTf)3." Chemistry Letters 38, no. 7 (July 5, 2009): 724–25. http://dx.doi.org/10.1246/cl.2009.724.
Повний текст джерелаDAIA, G. E., C. D. GABBUTT, J. D. HEPWORTH, B. M. HERON, D. E. HIBBS, and M. B. HURSTHOUSE. "ChemInform Abstract: The Directed Lithiation of Some 3-Acylchromone Acetals." ChemInform 29, no. 21 (June 22, 2010): no. http://dx.doi.org/10.1002/chin.199821125.
Повний текст джерелаGuss, L. T., L. V. Ershov, G. A. Bogdanova, and 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, no. 2 (February 1990): 183–88. http://dx.doi.org/10.1007/bf00499413.
Повний текст джерелаCambie, RC, SE Holroyd, PS Rutledge, and PD Woodgate. "Experiments Directed Towards the Synthesis of Anthracyclinones. XVII. Cyclization Reactions of Some Anthraquinone Conduritol Acetals." Australian Journal of Chemistry 46, no. 1 (1993): 37. http://dx.doi.org/10.1071/ch9930037.
Повний текст джерелаLiu, Yi-Wen, Rui-Jun Ma, Jia-Hang Yan, Zhu Zhou, and Bang-Guo Wei. "Asymmetric synthesis of (−)-sedacryptine through a diastereoselective Mannich reaction of N,O-acetals with ketones." Organic & Biomolecular Chemistry 16, no. 5 (2018): 771–79. http://dx.doi.org/10.1039/c7ob02989f.
Повний текст джерелаSomogyi, 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, no. 5 (September 2006): 1141–50. http://dx.doi.org/10.1002/jhet.5570430502.
Повний текст джерелаLöwe, Christiane, Gottfried Huttner, Laszlo Zsolnai, and Heinz Berke. "Acetalisierte Formylmangan-Komplexe / Acetals of Formyl Manganese Complexes." Zeitschrift für Naturforschung B 43, no. 1 (January 1, 1988): 25–30. http://dx.doi.org/10.1515/znb-1988-0106.
Повний текст джерелаMöhrle, Hans, та 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, № 8 (1 серпня 1987): 1032–34. http://dx.doi.org/10.1515/znb-1987-0818.
Повний текст джерелаVANKAR, Y. D., M. V. REDDY, and 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, no. 8 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199508076.
Повний текст джерелаXiao, Tiebo, Ping Zhang, Yang Xie, Jun Wang, and 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, no. 32 (2014): 6215–22. http://dx.doi.org/10.1039/c4ob00614c.
Повний текст джерелаDussault, P. H., R. J. Lee, J. A. Schultz, and Y. S. Suh. "Reaction of peroxyacetals with silyl ketene acetals: synthesis of 3-peroxyalkanoates and 3-peroxyalkanals." Tetrahedron Letters 41, no. 29 (July 2000): 5457–60. http://dx.doi.org/10.1016/s0040-4039(00)00914-x.
Повний текст джерелаGupta, Akhilesh K., R. T. Chakrasali, H. Ila, and 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, no. 02 (1989): 141–42. http://dx.doi.org/10.1055/s-1989-27179.
Повний текст джерелаCao, Zhicheng, Xin Deng, Chao Chen, Yonghong Liu, Lei Yu, and Xuefeng Jiang. "Synergetic catalysis of Se and Cu allowing diethoxylation of halomethylene ketones using O2 as the mild oxidant." Reaction Chemistry & Engineering 6, no. 3 (2021): 454–58. http://dx.doi.org/10.1039/d0re00471e.
Повний текст джерелаLyu, Longyun, Ming Yu Jin, Qijie He, Han Xie, Zhaoxiang Bian, and 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, no. 34 (2016): 8088–91. http://dx.doi.org/10.1039/c6ob01355d.
Повний текст джерелаKIM, S., J. H. PARK та 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, № 48 (20 серпня 2010): no. http://dx.doi.org/10.1002/chin.199348107.
Повний текст джерелаHuang, Yong Kui, Li Yu, Guo Bin Duan, Yun Zhi Wang, Ming Bo Xu, and Shui Jin Yang. "Catalytic Application of H3PW6Mo6O40/SiO2 in Synthesis of Acetals and Ketals." Advanced Materials Research 531 (June 2012): 304–7. http://dx.doi.org/10.4028/www.scientific.net/amr.531.304.
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