Статті в журналах з теми "Cyclopropane"
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Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Cyclopropane".
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Craig, Alexander J., та Bill C. Hawkins. "The Bonding and Reactivity of α-Carbonyl Cyclopropanes". Synthesis 52, № 01 (1 жовтня 2019): 27–39. http://dx.doi.org/10.1055/s-0039-1690695.
Повний текст джерелаDent, BR, B. Halton, and AMF Smith. "Synthesis and Trapping of Some Reactive Cyclopropenes." Australian Journal of Chemistry 39, no. 10 (1986): 1621. http://dx.doi.org/10.1071/ch9861621.
Повний текст джерелаGemoets, J. P., M. Bravo, C. E. McKenna, G. J. Leigh, and B. E. Smith. "Reduction of cyclopropene by NifV- and wild-type nitrogenases from Klebsiella pneumoniae." Biochemical Journal 258, no. 2 (March 1, 1989): 487–91. http://dx.doi.org/10.1042/bj2580487.
Повний текст джерелаKohout, Ladislav. "The synthesis of 5,6-cyclopropanocholestanes with oxygen functions in positions 3 and 7." Collection of Czechoslovak Chemical Communications 51, no. 2 (1986): 429–35. http://dx.doi.org/10.1135/cccc19860429.
Повний текст джерелаBen Hamadi, Naoufel, and Ahlem Guesmi. "Synthesis of New Spiro-Cyclopropanes Prepared by Non-Stabilized Diazoalkane Exhibiting an Extremely High Insecticidal Activity." Molecules 27, no. 8 (April 12, 2022): 2470. http://dx.doi.org/10.3390/molecules27082470.
Повний текст джерелаSingh, Satya Prakash, and Pompozhi Protasis Thankachan. "Hydroboration of Substituted Cyclopropane: A Density Functional Theory Study." Advances in Chemistry 2014 (August 18, 2014): 1–7. http://dx.doi.org/10.1155/2014/427396.
Повний текст джерелаTrudeau, Stéphane, and Pierre Deslongchamps. "Novel synthesis of a highly functionalized cyclopropane derivative." Canadian Journal of Chemistry 81, no. 9 (September 1, 2003): 1003–11. http://dx.doi.org/10.1139/v03-119.
Повний текст джерелаFadeev, Alexander A., Alexey O. Chagarovskiy, Anton S. Makarov, Irina I. Levina, Olga A. Ivanova, Maxim G. Uchuskin, and Igor V. Trushkov. "Synthesis of (Het)aryl 2-(2-hydroxyaryl)cyclopropyl Ketones." Molecules 25, no. 23 (December 5, 2020): 5748. http://dx.doi.org/10.3390/molecules25235748.
Повний текст джерелаRamnauth, Jailall, and Edward Lee-Ruff. "Photodecarbonylation of chiral cyclobutanones." Canadian Journal of Chemistry 75, no. 5 (May 1, 1997): 518–22. http://dx.doi.org/10.1139/v97-060.
Повний текст джерелаFinta, Zoltán, Zoltán Hell, Agnieszka Cwik, and László Tőke. "A Simple Synthesis of 1,1,2-tris-(Hydroxymethyl)-Cyclopropane and Its Dihalo Derivatives." Journal of Chemical Research 2002, no. 9 (September 2002): 459–60. http://dx.doi.org/10.3184/030823402103172653.
Повний текст джерелаRademacher, Paul. "Photoelectron Spectra of Cyclopropane and Cyclopropene Compounds." Chemical Reviews 103, no. 4 (April 2003): 933–76. http://dx.doi.org/10.1021/cr0100143.
Повний текст джерелаHassenrück, Jessica, and Valentin Wittmann. "Cyclopropene derivatives of aminosugars for metabolic glycoengineering." Beilstein Journal of Organic Chemistry 15 (March 4, 2019): 584–601. http://dx.doi.org/10.3762/bjoc.15.54.
Повний текст джерелаSimaan, Marwan, and Ilan Marek. "Diastereo- and enantioselective preparation of cyclopropanol derivatives." Beilstein Journal of Organic Chemistry 15 (March 21, 2019): 752–60. http://dx.doi.org/10.3762/bjoc.15.71.
Повний текст джерелаMatyas, Libor, Radek Pohl, and Alexander Kasal. "Neighboring Group Participation in 12,20-Dioxopregnanes." Natural Product Communications 2, no. 11 (November 2007): 1934578X0700201. http://dx.doi.org/10.1177/1934578x0700201108.
Повний текст джерелаSong, Xixi, Junbiao Chang, Yuanyuan Zhu, Shuang Zhao, and Minli Zhang. "Diastereoselective Synthesis of Spirobarbiturate-Cyclopropanes through Organobase-Mediated Spirocyclopropanation of Barbiturate-Based Olefins with Benzyl Chlorides." Synthesis 51, no. 04 (November 6, 2018): 899–906. http://dx.doi.org/10.1055/s-0037-1609637.
Повний текст джерелаAleksandrova, Anastasiia M., Alona S. Cherednichenko, and Yuliya V. Rassukana. "The Synthesis of Functionalized Dimethylphosphinoyl Cyclopropanes and Cyclobutanes." Journal of Organic and Pharmaceutical Chemistry 21, no. 4 (December 10, 2023): 36–42. http://dx.doi.org/10.24959/ophcj.23.299237.
Повний текст джерелаWanapun, D., K. A. Van Gorp, N. J. Mosey, M. A. Kerr, and T. K. Woo. "The mechanism of 1,3-dipolar cycloaddition reactions of cyclopropanes and nitrones A theoretical study." Canadian Journal of Chemistry 83, no. 10 (October 1, 2005): 1752–67. http://dx.doi.org/10.1139/v05-182.
Повний текст джерелаMiranda, Margarida S., Darío J. R. Duarte, Joaquim C. G. Esteves da Silva, and Joel F. Liebman. "Protonated heterocyclic derivatives of cyclopropane and cyclopropanone: classical species, alternate sites, and ring fragmentation." Canadian Journal of Chemistry 93, no. 7 (July 2015): 708–14. http://dx.doi.org/10.1139/cjc-2015-0029.
Повний текст джерелаBabu, Kaki Raveendra, Xin He, and Silong Xu. "Lewis Base Catalysis Based on Homoconjugate Addition: Rearrangement of Electron-Deficient Cyclopropanes and Their Derivatives." Synlett 31, no. 02 (November 20, 2019): 117–24. http://dx.doi.org/10.1055/s-0039-1690753.
Повний текст джерелаMlostoń, Grzegorz, Mateusz Kowalczyk, André U. Augustin, Peter G. Jones, and Daniel B. Werz. "Ferrocenyl-substituted tetrahydrothiophenes via formal [3 + 2]-cycloaddition reactions of ferrocenyl thioketones with donor–acceptor cyclopropanes." Beilstein Journal of Organic Chemistry 16 (June 10, 2020): 1288–95. http://dx.doi.org/10.3762/bjoc.16.109.
Повний текст джерелаLedingham, Edward, Christopher Merritt, Christopher Sumby, Michelle Taylor, and Ben Greatrex. "Stereoselective Cyclopropanation of (–)-Levoglucosenone Derivatives Using Sulfonium and Sulfoxonium Ylides." Synthesis 49, no. 12 (March 17, 2017): 2652–62. http://dx.doi.org/10.1055/s-0036-1588971.
Повний текст джерелаIvanova, Olga, Vladimir Andronov, Irina Levina, Alexey Chagarovskiy, Leonid Voskressensky, and Igor Trushkov. "Convenient Synthesis of Functionalized Cyclopropa[c]coumarin-1a-carboxylates." Molecules 24, no. 1 (December 24, 2018): 57. http://dx.doi.org/10.3390/molecules24010057.
Повний текст джерелаVereshchagin, Anatolii N., Michail N. Elinson, Nikita O. Stepanov, and Gennady I. Nikishin. "New Way to Substitute Tetracyanocyclopropanes: One-Pot Cascade Assembling of Carbonyls and Malononitrile by the Only Bromine Direct Action." ISRN Organic Chemistry 2011 (July 26, 2011): 1–5. http://dx.doi.org/10.5402/2011/469453.
Повний текст джерелаFang, Zeguo, Nawaf Al-Maharik, Peer Kirsch, Matthias Bremer, Alexandra M. Z. Slawin, and David O’Hagan. "Synthesis of organic liquid crystals containing selectively fluorinated cyclopropanes." Beilstein Journal of Organic Chemistry 16 (April 14, 2020): 674–80. http://dx.doi.org/10.3762/bjoc.16.65.
Повний текст джерелаZhang, Junliang, and Yuanjing Xiao. "ChemInform Abstract: Cyclization of Cyclopropane- or Cyclopropene-Containing Compounds." ChemInform 41, no. 38 (August 26, 2010): no. http://dx.doi.org/10.1002/chin.201038242.
Повний текст джерелаDenson, J. S. "Cyclopropane." International Anesthesiology Clinics 36, no. 4 (1998): 61–82. http://dx.doi.org/10.1097/00004311-199803640-00008.
Повний текст джерелаLamberty, J. M. "Cyclopropane." Anaesthesia 42, no. 2 (February 1987): 212–13. http://dx.doi.org/10.1111/j.1365-2044.1987.tb03011.x.
Повний текст джерелаBall, C., and R. N. Westhorpe. "Cyclopropane." Anaesthesia and Intensive Care 34, no. 6 (December 2006): 701. http://dx.doi.org/10.1177/0310057x0603400621.
Повний текст джерелаBoichenko, Maksim A., Andrey Yu Plodukhin, Vitaly V. Shorokhov, Danyla S. Lebedev, Anastasya V. Filippova, Sergey S. Zhokhov, Elena A. Tarasenko, Victor B. Rybakov, Igor V. Trushkov, and Olga A. Ivanova. "Synthesis of 1,5-Substituted Pyrrolidin-2-ones from Donor–Acceptor Cyclopropanes and Anilines/Benzylamines." Molecules 27, no. 23 (December 2, 2022): 8468. http://dx.doi.org/10.3390/molecules27238468.
Повний текст джерелаMato, Mauro, Inmaculada Martín-Torres, Bart Herlé, and Antonio M. Echavarren. "Cyclopropane–alkene metathesis by gold(i)-catalyzed decarbenation of persistent cyclopropanes." Organic & Biomolecular Chemistry 17, no. 17 (2019): 4216–19. http://dx.doi.org/10.1039/c9ob00359b.
Повний текст джерелаGavrus, Delia. "Envisioning Cyclopropane: Scientific Product or Medical Technology?" Scientia Canadensis 33, no. 1 (February 3, 2011): 3–28. http://dx.doi.org/10.7202/1000843ar.
Повний текст джерелаDon Lawson, Chioma, Max Maza-Iglesias, Muthana Sirhan, Jumaa Al Dulayymi та Mark Baird. "The Synthesis of Single Enantiomers of α-Mycolic Acids of Mycobacterium tuberculosis and Related Organisms, with Alternative Cyclopropane Stereochemistries". SynOpen 01, № 01 (березень 2017): 0103–16. http://dx.doi.org/10.1055/s-0036-1588556.
Повний текст джерелаMead, Keith, and Yahaira Reyes. "Acetoxy-Substituted Cyclopropane Dicarbonyls as Stable Donor–Acceptor–Acceptor Cyclopropanes." Synthesis 47, no. 19 (June 25, 2015): 3020–26. http://dx.doi.org/10.1055/s-0034-1379934.
Повний текст джерелаBen Hamadi, Naoufel, Ahlem Guesmi, and Wided Nouira. "Asymmetric one-pot synthesis of cyclopropanes." Macedonian Journal of Chemistry and Chemical Engineering 35, no. 1 (April 18, 2016): 45. http://dx.doi.org/10.20450/mjcce.2016.835.
Повний текст джерелаHerraiz, Ana G., and Marcos G. Suero. "New Alkene Cyclopropanation Reactions Enabled by Photoredox Catalysis via Radical Carbenoids." Synthesis 51, no. 14 (June 11, 2019): 2821–28. http://dx.doi.org/10.1055/s-0037-1611872.
Повний текст джерелаAltamore, Timothy M., Oanh T. K. Nguyen, Quentin I. Churches, Kate Cavanagh, Xuan T. T. Nguyen, Sandhya A. M. Duggan, Guy Y. Krippner, and Peter J. Duggan. "Concise Synthesis of Enantiomerically Pure (1'S,2'R)- and (1'R,2'S)-2S-Amino-3-(2'-aminomethyl-cyclopropyl)propionic Acid: Two E-Diastereoisomers of 4,5-Methano-L-lysine." Australian Journal of Chemistry 66, no. 9 (2013): 1105. http://dx.doi.org/10.1071/ch13309.
Повний текст джерелаBilera, Igor V. "The Formation of Small Amounts of Cyclopropane during Pulsed Pyrolysis of C4–C5 Acyclic Alkanes in the Adiabatic Compression Reactor." Reactions 4, no. 3 (July 19, 2023): 381–97. http://dx.doi.org/10.3390/reactions4030023.
Повний текст джерелаZhuo, Chun-Xiang, and Jia-Le Wang. "Catalytic Deoxygenative Cyclopropanation of 1,2-Dicarbonyl or Monocarbonyl Compounds via Molybdenum Catalysis." Synlett 33, no. 07 (November 13, 2021): 599–608. http://dx.doi.org/10.1055/a-1696-4553.
Повний текст джерелаLuo, Hui-Xin, You-Hong Niu, Xiao-Ping Cao, and Xin-Shan Ye. "Cyclopropenes for the Synthesis of Cyclopropane-Fused Dihydroquinolines and Benzazepines." Advanced Synthesis & Catalysis 357, no. 13 (September 10, 2015): 2893–902. http://dx.doi.org/10.1002/adsc.201500203.
Повний текст джерелаHara, Koji, Edmond I. Eger, Michael J. Laster, and R. Adron Harris. "Nonhalogenated Alkanes Cyclopropane and Butane Affect Neurotransmitter-gated Ion Channel and G-protein–coupled Receptors." Anesthesiology 97, no. 6 (December 1, 2002): 1512–20. http://dx.doi.org/10.1097/00000542-200212000-00025.
Повний текст джерелаLiu, Yu, Qiao-Lin Wang, Zan Chen, Cong-Shan Zhou, Bi-Quan Xiong, Pan-Liang Zhang, Chang-An Yang, and Quan Zhou. "Oxidative radical ring-opening/cyclization of cyclopropane derivatives." Beilstein Journal of Organic Chemistry 15 (January 28, 2019): 256–78. http://dx.doi.org/10.3762/bjoc.15.23.
Повний текст джерелаBarkan, Daniel, Vivek Rao, George D. Sukenick, and Michael S. Glickman. "Redundant Function of cmaA2 and mmaA2 in Mycobacterium tuberculosis cis Cyclopropanation of Oxygenated Mycolates." Journal of Bacteriology 192, no. 14 (May 14, 2010): 3661–68. http://dx.doi.org/10.1128/jb.00312-10.
Повний текст джерелаSathishkannan, Gopal, V. John Tamilarasan, and Kannupal Srinivasan. "Nucleophilic ring-opening reactions of trans-2-aroyl-3-aryl-cyclopropane-1,1-dicarboxylates with hydrazines." Organic & Biomolecular Chemistry 15, no. 6 (2017): 1400–1406. http://dx.doi.org/10.1039/c6ob02552h.
Повний текст джерелаJalkanen, K. J., J. D. Gale, G. J. Jalkanen, D. F. McIntosh, A. A. El-Azhary, and G. M. Jensen. "trans-1,2-Dicyano-cyclopropane and other cyano-cyclopropane derivatives." Theoretical Chemistry Accounts 119, no. 1-3 (October 17, 2007): 211–29. http://dx.doi.org/10.1007/s00214-007-0391-6.
Повний текст джерелаFreedman, Teresa B., Diane L. Hausch, Steven J. Cianciosi, and John E. Baldwin. "Kinetics of thermal racemization of (2S,3S)-1-13C-1,2,3-d3-cyclopropane followed by vibrational circular dichroism spectroscopy." Canadian Journal of Chemistry 76, no. 6 (June 1, 1998): 806–10. http://dx.doi.org/10.1139/v98-070.
Повний текст джерелаBudynina, Ekaterina, Konstantin Ivanov, Ivan Sorokin, and Mikhail Melnikov. "Ring Opening of Donor–Acceptor Cyclopropanes with N-Nucleophiles." Synthesis 49, no. 14 (May 18, 2017): 3035–68. http://dx.doi.org/10.1055/s-0036-1589021.
Повний текст джерелаWang, Lizhong, Zhenjie Su, Siran Qian, Weijian Ye, and Cunde Wang. "Efficient Preparation of 2,3-Disubstituted Cyclopropane-1-Carbonitriles via Selective Decarboxylation of 1-Cyanocyclopropane-1-Carboxylates." Journal of Chemical Research 41, no. 11 (November 2017): 636–40. http://dx.doi.org/10.3184/174751917x15094552081161.
Повний текст джерелаSedenkova, Kseniya N., Kristian S. Andriasov, Tamara S. Kuznetsova, and Elena B. Averina. "Oxyfunctionalization of CH2-Group Activated by Adjacent Three-Membered Ring." Current Organic Synthesis 15, no. 4 (June 12, 2018): 515–32. http://dx.doi.org/10.2174/1570179415666180405113158.
Повний текст джерелаXie, Yaoming, and Henry F. Schaefer. "Aluminirene (HAlC2H2) and aluminirane (HAlC2H4): aluminum-substituted counterparts of cyclopropene and cyclopropane." Journal of the American Chemical Society 112, no. 14 (July 1990): 5393–400. http://dx.doi.org/10.1021/ja00170a001.
Повний текст джерелаAl Dulayymi, Ahmad R., and Mark S. Baird. "2-Vinyl-1,1,2-trihalocyclopropanes-valuable five carbon cyclopropane and cyclopropene synthetic intermediates." Tetrahedron 52, no. 33 (August 1996): 10955–68. http://dx.doi.org/10.1016/0040-4020(96)00592-3.
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