Статті в журналах з теми "Versatile intermediates"
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Boeske, Juergen, Edgar Niecke, Edgar Ocando-Mavarez, Jean Pierre Majoral, and Guy Bertrand. "Phosphonitriles: versatile intermediates." Inorganic Chemistry 25, no. 16 (July 1986): 2695–98. http://dx.doi.org/10.1021/ic00236a008.
Повний текст джерелаBelletire, J. L. "Acylcyanamides: Versatile Synthetic Intermediates." Synthetic Communications 18, no. 16-17 (November 1988): 2063–71. http://dx.doi.org/10.1080/00397918808068275.
Повний текст джерелаR. Katritzky, Alan, Adam S. Vincek, and Peter J. Steel. "Triphenylphosphoranylidene Substituted Heterocycles as Versatile Intermediates." HETEROCYCLES 76, no. 2 (2008): 1401. http://dx.doi.org/10.3987/com-08-s(f)12.
Повний текст джерелаBritten, Thomas K., Paul D. Kemmitt, Nathan R. Halcovitch, and Susannah C. Coote. "1,2-Dihydropyridazines as Versatile Synthetic Intermediates." Synlett 31, no. 05 (February 13, 2020): 459–62. http://dx.doi.org/10.1055/s-0039-1690825.
Повний текст джерелаBari, Ahmed. "Monosaccharidic Push-pull Butadienes: Versatile Synthetic Intermediates." Zeitschrift für Naturforschung B 69, no. 1 (January 1, 2014): 98–102. http://dx.doi.org/10.5560/znb.2014-3179.
Повний текст джерелаAttanasi, Orazio A., and Luciano Caglioti. "CONJUGATED AZOALKENES: ATTRACTIVE PRODUCTS AND VERSATILE INTERMEDIATES." Organic Preparations and Procedures International 18, no. 5 (October 1986): 299–327. http://dx.doi.org/10.1080/00304948609356836.
Повний текст джерелаFlashman, Emily, and Christopher J. Schofield. "The most versatile of all reactive intermediates?" Nature Chemical Biology 3, no. 2 (February 2007): 86–87. http://dx.doi.org/10.1038/nchembio0207-86.
Повний текст джерелаZellner, Armin, and Manfred Schlosser. "Pentadienyltitaniums as Versatile Intermediates: Regio- and Stereoselectivities." Synlett 2001, Special Issue (2001): 1016–18. http://dx.doi.org/10.1055/s-2001-14650.
Повний текст джерелаBarrett, Anthony G. M., and Gregory G. Graboski. "Conjugated nitroalkenes: versatile intermediates in organic synthesis." Chemical Reviews 86, no. 5 (October 1986): 751–62. http://dx.doi.org/10.1021/cr00075a002.
Повний текст джерелаMichael, J. P., C. B. de Koning, D. Gravestock, G. D. Hosken, A. S. Howard, C. M. Jungmann, R. W. M. Krause, A. S. Parsons, S. C. Pelly, and T. V. Stanbury. "Enaminones: versatile intermediates for natural product synthesis." Pure and Applied Chemistry 71, no. 6 (June 30, 1999): 979–88. http://dx.doi.org/10.1351/pac199971060979.
Повний текст джерелаJoergensen, M., K. A. Lerstrup, and K. Bechgaard. "Mesoions as versatile intermediates in tetrathiafulvalene synthesis." Journal of Organic Chemistry 56, no. 19 (September 1991): 5684–88. http://dx.doi.org/10.1021/jo00019a041.
Повний текст джерелаChemla, Fabrice. "α-Oxy sulfones and sulfoximines: versatile intermediates". Journal of the Chemical Society, Perkin Transactions 1, № 3 (10 січня 2002): 275–99. http://dx.doi.org/10.1039/b009523k.
Повний текст джерелаLamberth, Clemens. "Organic Isocyanates and Isothiocyanates: Versatile Intermediates in Agrochemistry." Synthesis 54, no. 05 (October 26, 2021): 1250–60. http://dx.doi.org/10.1055/a-1678-8528.
Повний текст джерелаWarkentin, John. "Δ3-1,3,4-Oxadiazolines.† Versatile sources of reactive intermediates". Journal of the Chemical Society, Perkin Transactions 1, № 14 (2000): 2161–69. http://dx.doi.org/10.1039/b000930j.
Повний текст джерелаRedely, D. Bhaskar, M. V. Ramana Redely, and V. Padmavathi. "Cyclohexanone Gem-Dicarboxylates - Versatile Intermediates for Fused Heterocycles." Synthetic Communications 29, no. 4 (February 1999): 667–76. http://dx.doi.org/10.1080/00397919908085815.
Повний текст джерелаHavel, Václav, Tereza Sadilová, and Vladimír Šindelář. "Unsubstituted Bambusurils: Post-Macrocyclization Modification of Versatile Intermediates." ACS Omega 3, no. 4 (April 27, 2018): 4657–63. http://dx.doi.org/10.1021/acsomega.8b00497.
Повний текст джерелаKrafft, Grant A., Ester A. Garcia, Anil Guram, Brian O'Shaughnessy, and Xialong Xu. "Simplified cytochalasins. 1. Synthesis of versatile perhydroisoindolone intermediates." Tetrahedron Letters 27, no. 24 (1986): 2691–94. http://dx.doi.org/10.1016/s0040-4039(00)84618-3.
Повний текст джерелаvan de Wouw, Heidi L., and Rebekka S. Klausen. "BN Polystyrenes: Emerging Optical Materials and Versatile Intermediates." Journal of Organic Chemistry 84, no. 3 (January 8, 2019): 1117–25. http://dx.doi.org/10.1021/acs.joc.8b02921.
Повний текст джерелаIrwin, Jacob L., and Michael S. Sherburn. "Monolithiocavitands: Versatile Intermediates for New Cavitand-Based Hosts." Organic Letters 3, no. 2 (January 2001): 225–27. http://dx.doi.org/10.1021/ol006881w.
Повний текст джерелаWaldvogel, Siegfried R., and Sabine Möhle. "Versatile Electrochemical CH Amination via Zincke Intermediates." Angewandte Chemie International Edition 54, no. 22 (May 12, 2015): 6398–99. http://dx.doi.org/10.1002/anie.201502638.
Повний текст джерелаZhang, Shu Xin. "Research on Synthesis of Benzoic Acids Intermediates." Applied Mechanics and Materials 192 (July 2012): 270–74. http://dx.doi.org/10.4028/www.scientific.net/amm.192.270.
Повний текст джерелаRoy, Tony, and Akkattu T. Biju. "Recent advances in molecular rearrangements involving aryne intermediates." Chemical Communications 54, no. 21 (2018): 2580–94. http://dx.doi.org/10.1039/c7cc09122b.
Повний текст джерелаDucrot, Paul-Henri, Anne-Claire Hervier, and Jean-Yves Lallemand. "Stereoselective Synthesis of Versatile Intermediates for Clerodanes Total synthesis." Synthetic Communications 26, no. 23 (December 1996): 4447–57. http://dx.doi.org/10.1080/00397919608003847.
Повний текст джерелаCordero, Franca M., Francesco De Sarlo, and Alberto Brandi. "5-Spirocyclopropane Isoxazolidines as Versatile Intermediates in Organic Synthesis." Monatshefte f�r Chemie / Chemical Monthly 135, no. 6 (June 1, 2004): 649–69. http://dx.doi.org/10.1007/s00706-003-0150-x.
Повний текст джерелаMukaiyama, Teruaki, and Hokuto Yamabe. "Alkyl Phosphinites: Versatile Synthetic Intermediates for Dehydration Condensation Reactions." Chemistry Letters 36, no. 1 (January 2007): 2–7. http://dx.doi.org/10.1246/cl.2007.2.
Повний текст джерелаSchmidt, Richard R. "Functionally Substituted Vinyl Carbanions Versatile Intermediates in Heterocyclic Synthesis." Bulletin des Sociétés Chimiques Belges 92, no. 9 (September 1, 2010): 825–36. http://dx.doi.org/10.1002/bscb.19830920909.
Повний текст джерелаMichael, Joseph P., Charles B. De Koning, David Gravestock, Gladys D. Hosken, Arthur S. Howard, Christa M. Jungmann, Rui W. M. Krause, Andrew S. Parsons, Stephen C. Pelly, and Trevor V. Stanbury. "ChemInform Abstract: Enaminones: Versatile Intermediates for Natural Product Synthesis." ChemInform 31, no. 4 (June 11, 2010): no. http://dx.doi.org/10.1002/chin.200004280.
Повний текст джерелаZellner, Armin, and Manfred Schlosser. "ChemInform Abstract: Pentadienyltitaniums as Versatile Intermediates: Regio- and Stereoselectivities." ChemInform 32, no. 40 (May 24, 2010): no. http://dx.doi.org/10.1002/chin.200140064.
Повний текст джерелаJOERGENSEN, M., K. A. LERSTRUP, and K. BECHGAARD. "ChemInform Abstract: Mesoions as Versatile Intermediates in Tetrathiafulvalene Synthesis." ChemInform 23, no. 6 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199206174.
Повний текст джерелаChemla, Fabrice. "ChemInform Abstract: α-Oxy Sulfones and Sulfoximines: Versatile Intermediates". ChemInform 33, № 24 (21 травня 2010): no. http://dx.doi.org/10.1002/chin.200224251.
Повний текст джерелаEvano, Gwilherm, Morgan Lecomte, Pierre Thilmany, and Cédric Theunissen. "Keteniminium Ions: Unique and Versatile Reactive Intermediates for Chemical Synthesis." Synthesis 49, no. 15 (July 17, 2017): 3183–214. http://dx.doi.org/10.1055/s-0036-1588452.
Повний текст джерелаTian, Feitao, Guobing Yan та Jian Yu. "Recent advances in the synthesis and applications of α-(trifluoromethyl)styrenes in organic synthesis". Chemical Communications 55, № 90 (2019): 13486–505. http://dx.doi.org/10.1039/c9cc06465f.
Повний текст джерелаIwanejko, Jakub, and Elżbieta Wojaczyńska. "Cyclic imines – preparation and application in synthesis." Organic & Biomolecular Chemistry 16, no. 40 (2018): 7296–314. http://dx.doi.org/10.1039/c8ob01874j.
Повний текст джерелаDong, Kuiyong, Mengting Liu, and Xinfang Xu. "Recent Advances in Catalytic Alkyne Transformation via Copper Carbene Intermediates." Molecules 27, no. 10 (May 11, 2022): 3088. http://dx.doi.org/10.3390/molecules27103088.
Повний текст джерелаLiew, Sean K., Aleksandra Holownia, Diego B. Diaz, Philip A. Cistrone, Philip E. Dawson, and Andrei K. Yudin. "Borylated oximes: versatile building blocks for organic synthesis." Chem. Commun. 53, no. 81 (2017): 11237–40. http://dx.doi.org/10.1039/c7cc06579e.
Повний текст джерелаBerger, Olivier, and Jean-Luc Montchamp. "General synthesis of P-stereogenic compounds: the menthyl phosphinate approach." Organic & Biomolecular Chemistry 14, no. 31 (2016): 7552–62. http://dx.doi.org/10.1039/c6ob01413e.
Повний текст джерелаBayer, Patrick, Josef Schachtner, Michal Májek, and Axel Jacobi von Wangelin. "Visible light-mediated photo-oxygenation of arylcyclohexenes." Organic Chemistry Frontiers 6, no. 16 (2019): 2877–83. http://dx.doi.org/10.1039/c9qo00493a.
Повний текст джерелаSantamaría, Javier, and Enrique Aguilar. "Beyond Fischer and Schrock carbenes: non-heteroatom-stabilized group 6 metal carbene complexes – a general overview." Organic Chemistry Frontiers 3, no. 11 (2016): 1561–88. http://dx.doi.org/10.1039/c6qo00206d.
Повний текст джерелаHearne, Zoë, and Chao-Jun Li. "Palladium-catalysed atom-economical synthesis of conjugated dienals from terminal acetylenes and acrolein." Chemical Communications 53, no. 45 (2017): 6136–39. http://dx.doi.org/10.1039/c7cc02767b.
Повний текст джерелаIftikhar, Ramsha, Aqsa Mazhar, Muhammad Saqlain Iqbal, Faiza Zahid Khan, Syed Hassan Askary, and Hifza Sibtain. "Ring forming transformations of ynamides via cycloaddition." RSC Advances 13, no. 16 (2023): 10715–56. http://dx.doi.org/10.1039/d3ra00139c.
Повний текст джерелаTurrini, Nikolaus G., Răzvan C. Cioc, Daan J. H. van der Niet, Eelco Ruijter, Romano V. A. Orru, Mélanie Hall та Kurt Faber. "Biocatalytic access to nonracemic γ-oxo esters via stereoselective reduction using ene-reductases". Green Chemistry 19, № 2 (2017): 511–18. http://dx.doi.org/10.1039/c6gc02493a.
Повний текст джерелаPrasad, Sure Siva, Dirgha Raj Joshi, Jeong Hwa Lee, and Ikyon Kim. "One-pot access to 2-amino-3-arylbenzofurans: direct entry to polyheterocyclic chemical space." Organic & Biomolecular Chemistry 18, no. 40 (2020): 8119–40. http://dx.doi.org/10.1039/d0ob01715a.
Повний текст джерелаLynch, Dylan M., and Eoin M. Scanlan. "Thiyl Radicals: Versatile Reactive Intermediates for Cyclization of Unsaturated Substrates." Molecules 25, no. 13 (July 7, 2020): 3094. http://dx.doi.org/10.3390/molecules25133094.
Повний текст джерелаX. Xiang, Alan, Ricardo Lira, Konstantinos A. Agrios, Thomas Doundoulakis, Klaus B. Simonsen, and Stephen E. Webber. "An Efficient Synthesis of (±)-Myxopyronin B via Versatile Pyridone Intermediates." HETEROCYCLES 68, no. 6 (2006): 1099. http://dx.doi.org/10.3987/com-06-10733.
Повний текст джерелаBarcelo, Gérard, Jean-Pierre Senet, and Gérard Sennyey. "1,2,2,2-Tetrachloroethyl Carbamates: Versatile Intermediates for the Synthesis ofN-Nitrosoureas." Synthesis 1987, no. 11 (1987): 1027–29. http://dx.doi.org/10.1055/s-1987-28160.
Повний текст джерелаDondoni, Alessandro, and Alberto Marra. "Thiazolylketoses: a new class of versatile intermediates for glycoside synthesis." Chemical Communications, no. 21 (1999): 2133–45. http://dx.doi.org/10.1039/a903758f.
Повний текст джерелаMaduli, Elvis J. M., Steven J. Edeson, Stephen Swanson, Panayiotis A. Procopiou, and Joseph P. A. Harrity. "2-Iodoisatogens: Versatile Intermediates for the Synthesis of Nitrogen Heterocycles." Organic Letters 17, no. 2 (December 23, 2014): 390–92. http://dx.doi.org/10.1021/ol503487f.
Повний текст джерелаKataja, Antti O., and Géraldine Masson. "Imine and iminium precursors as versatile intermediates in enantioselective organocatalysis." Tetrahedron 70, no. 46 (November 2014): 8783–815. http://dx.doi.org/10.1016/j.tet.2014.06.101.
Повний текст джерелаWu, Chien-Hsin, Li-Yun Chen, Ru-Jong Jeng, and Shenghong A. Dai. "100% Atom-Economy Efficiency of Recycling Polycarbonate into Versatile Intermediates." ACS Sustainable Chemistry & Engineering 6, no. 7 (May 28, 2018): 8964–75. http://dx.doi.org/10.1021/acssuschemeng.8b01326.
Повний текст джерелаMartin, Stephen F., and Michael P. Dwyer. "Iodocyclopropanes as versatile intermediates for the synthesis of substituted cyclopropanes." Tetrahedron Letters 39, no. 12 (March 1998): 1521–24. http://dx.doi.org/10.1016/s0040-4039(98)00072-0.
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