Zeitschriftenartikel zum Thema „Cyclopropane“
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Craig, Alexander J., und Bill C. Hawkins. „The Bonding and Reactivity of α-Carbonyl Cyclopropanes“. Synthesis 52, Nr. 01 (01.10.2019): 27–39. http://dx.doi.org/10.1055/s-0039-1690695.
Dent, BR, B. Halton und AMF Smith. „Synthesis and Trapping of Some Reactive Cyclopropenes“. Australian Journal of Chemistry 39, Nr. 10 (1986): 1621. http://dx.doi.org/10.1071/ch9861621.
Gemoets, J. P., M. Bravo, C. E. McKenna, G. J. Leigh und B. E. Smith. „Reduction of cyclopropene by NifV- and wild-type nitrogenases from Klebsiella pneumoniae“. Biochemical Journal 258, Nr. 2 (01.03.1989): 487–91. http://dx.doi.org/10.1042/bj2580487.
Kohout, Ladislav. „The synthesis of 5,6-cyclopropanocholestanes with oxygen functions in positions 3 and 7“. Collection of Czechoslovak Chemical Communications 51, Nr. 2 (1986): 429–35. http://dx.doi.org/10.1135/cccc19860429.
Ben Hamadi, Naoufel, und Ahlem Guesmi. „Synthesis of New Spiro-Cyclopropanes Prepared by Non-Stabilized Diazoalkane Exhibiting an Extremely High Insecticidal Activity“. Molecules 27, Nr. 8 (12.04.2022): 2470. http://dx.doi.org/10.3390/molecules27082470.
Singh, Satya Prakash, und Pompozhi Protasis Thankachan. „Hydroboration of Substituted Cyclopropane: A Density Functional Theory Study“. Advances in Chemistry 2014 (18.08.2014): 1–7. http://dx.doi.org/10.1155/2014/427396.
Trudeau, Stéphane, und Pierre Deslongchamps. „Novel synthesis of a highly functionalized cyclopropane derivative“. Canadian Journal of Chemistry 81, Nr. 9 (01.09.2003): 1003–11. http://dx.doi.org/10.1139/v03-119.
Fadeev, Alexander A., Alexey O. Chagarovskiy, Anton S. Makarov, Irina I. Levina, Olga A. Ivanova, Maxim G. Uchuskin und Igor V. Trushkov. „Synthesis of (Het)aryl 2-(2-hydroxyaryl)cyclopropyl Ketones“. Molecules 25, Nr. 23 (05.12.2020): 5748. http://dx.doi.org/10.3390/molecules25235748.
Ramnauth, Jailall, und Edward Lee-Ruff. „Photodecarbonylation of chiral cyclobutanones“. Canadian Journal of Chemistry 75, Nr. 5 (01.05.1997): 518–22. http://dx.doi.org/10.1139/v97-060.
Finta, Zoltán, Zoltán Hell, Agnieszka Cwik und László Tőke. „A Simple Synthesis of 1,1,2-tris-(Hydroxymethyl)-Cyclopropane and Its Dihalo Derivatives“. Journal of Chemical Research 2002, Nr. 9 (September 2002): 459–60. http://dx.doi.org/10.3184/030823402103172653.
Rademacher, Paul. „Photoelectron Spectra of Cyclopropane and Cyclopropene Compounds“. Chemical Reviews 103, Nr. 4 (April 2003): 933–76. http://dx.doi.org/10.1021/cr0100143.
Hassenrück, Jessica, und Valentin Wittmann. „Cyclopropene derivatives of aminosugars for metabolic glycoengineering“. Beilstein Journal of Organic Chemistry 15 (04.03.2019): 584–601. http://dx.doi.org/10.3762/bjoc.15.54.
Simaan, Marwan, und Ilan Marek. „Diastereo- and enantioselective preparation of cyclopropanol derivatives“. Beilstein Journal of Organic Chemistry 15 (21.03.2019): 752–60. http://dx.doi.org/10.3762/bjoc.15.71.
Matyas, Libor, Radek Pohl und Alexander Kasal. „Neighboring Group Participation in 12,20-Dioxopregnanes“. Natural Product Communications 2, Nr. 11 (November 2007): 1934578X0700201. http://dx.doi.org/10.1177/1934578x0700201108.
Song, Xixi, Junbiao Chang, Yuanyuan Zhu, Shuang Zhao und Minli Zhang. „Diastereoselective Synthesis of Spirobarbiturate-Cyclopropanes through Organobase-Mediated Spirocyclopropanation of Barbiturate-Based Olefins with Benzyl Chlorides“. Synthesis 51, Nr. 04 (06.11.2018): 899–906. http://dx.doi.org/10.1055/s-0037-1609637.
Aleksandrova, Anastasiia M., Alona S. Cherednichenko und Yuliya V. Rassukana. „The Synthesis of Functionalized Dimethylphosphinoyl Cyclopropanes and Cyclobutanes“. Journal of Organic and Pharmaceutical Chemistry 21, Nr. 4 (10.12.2023): 36–42. http://dx.doi.org/10.24959/ophcj.23.299237.
Wanapun, D., K. A. Van Gorp, N. J. Mosey, M. A. Kerr und T. K. Woo. „The mechanism of 1,3-dipolar cycloaddition reactions of cyclopropanes and nitrones A theoretical study“. Canadian Journal of Chemistry 83, Nr. 10 (01.10.2005): 1752–67. http://dx.doi.org/10.1139/v05-182.
Miranda, Margarida S., Darío J. R. Duarte, Joaquim C. G. Esteves da Silva und Joel F. Liebman. „Protonated heterocyclic derivatives of cyclopropane and cyclopropanone: classical species, alternate sites, and ring fragmentation“. Canadian Journal of Chemistry 93, Nr. 7 (Juli 2015): 708–14. http://dx.doi.org/10.1139/cjc-2015-0029.
Babu, Kaki Raveendra, Xin He und Silong Xu. „Lewis Base Catalysis Based on Homoconjugate Addition: Rearrangement of Electron-Deficient Cyclopropanes and Their Derivatives“. Synlett 31, Nr. 02 (20.11.2019): 117–24. http://dx.doi.org/10.1055/s-0039-1690753.
Mlostoń, Grzegorz, Mateusz Kowalczyk, André U. Augustin, Peter G. Jones und 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 (10.06.2020): 1288–95. http://dx.doi.org/10.3762/bjoc.16.109.
Ledingham, Edward, Christopher Merritt, Christopher Sumby, Michelle Taylor und Ben Greatrex. „Stereoselective Cyclopropanation of (–)-Levoglucosenone Derivatives Using Sulfonium and Sulfoxonium Ylides“. Synthesis 49, Nr. 12 (17.03.2017): 2652–62. http://dx.doi.org/10.1055/s-0036-1588971.
Ivanova, Olga, Vladimir Andronov, Irina Levina, Alexey Chagarovskiy, Leonid Voskressensky und Igor Trushkov. „Convenient Synthesis of Functionalized Cyclopropa[c]coumarin-1a-carboxylates“. Molecules 24, Nr. 1 (24.12.2018): 57. http://dx.doi.org/10.3390/molecules24010057.
Vereshchagin, Anatolii N., Michail N. Elinson, Nikita O. Stepanov und 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 (26.07.2011): 1–5. http://dx.doi.org/10.5402/2011/469453.
Fang, Zeguo, Nawaf Al-Maharik, Peer Kirsch, Matthias Bremer, Alexandra M. Z. Slawin und David O’Hagan. „Synthesis of organic liquid crystals containing selectively fluorinated cyclopropanes“. Beilstein Journal of Organic Chemistry 16 (14.04.2020): 674–80. http://dx.doi.org/10.3762/bjoc.16.65.
Zhang, Junliang, und Yuanjing Xiao. „ChemInform Abstract: Cyclization of Cyclopropane- or Cyclopropene-Containing Compounds“. ChemInform 41, Nr. 38 (26.08.2010): no. http://dx.doi.org/10.1002/chin.201038242.
Denson, J. S. „Cyclopropane“. International Anesthesiology Clinics 36, Nr. 4 (1998): 61–82. http://dx.doi.org/10.1097/00004311-199803640-00008.
Lamberty, J. M. „Cyclopropane“. Anaesthesia 42, Nr. 2 (Februar 1987): 212–13. http://dx.doi.org/10.1111/j.1365-2044.1987.tb03011.x.
Ball, C., und R. N. Westhorpe. „Cyclopropane“. Anaesthesia and Intensive Care 34, Nr. 6 (Dezember 2006): 701. http://dx.doi.org/10.1177/0310057x0603400621.
Boichenko, 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 und Olga A. Ivanova. „Synthesis of 1,5-Substituted Pyrrolidin-2-ones from Donor–Acceptor Cyclopropanes and Anilines/Benzylamines“. Molecules 27, Nr. 23 (02.12.2022): 8468. http://dx.doi.org/10.3390/molecules27238468.
Mato, Mauro, Inmaculada Martín-Torres, Bart Herlé und Antonio M. Echavarren. „Cyclopropane–alkene metathesis by gold(i)-catalyzed decarbenation of persistent cyclopropanes“. Organic & Biomolecular Chemistry 17, Nr. 17 (2019): 4216–19. http://dx.doi.org/10.1039/c9ob00359b.
Gavrus, Delia. „Envisioning Cyclopropane: Scientific Product or Medical Technology?“ Scientia Canadensis 33, Nr. 1 (03.02.2011): 3–28. http://dx.doi.org/10.7202/1000843ar.
Don Lawson, Chioma, Max Maza-Iglesias, Muthana Sirhan, Jumaa Al Dulayymi und Mark Baird. „The Synthesis of Single Enantiomers of α-Mycolic Acids of Mycobacterium tuberculosis and Related Organisms, with Alternative Cyclopropane Stereochemistries“. SynOpen 01, Nr. 01 (März 2017): 0103–16. http://dx.doi.org/10.1055/s-0036-1588556.
Mead, Keith, und Yahaira Reyes. „Acetoxy-Substituted Cyclopropane Dicarbonyls as Stable Donor–Acceptor–Acceptor Cyclopropanes“. Synthesis 47, Nr. 19 (25.06.2015): 3020–26. http://dx.doi.org/10.1055/s-0034-1379934.
Ben Hamadi, Naoufel, Ahlem Guesmi und Wided Nouira. „Asymmetric one-pot synthesis of cyclopropanes“. Macedonian Journal of Chemistry and Chemical Engineering 35, Nr. 1 (18.04.2016): 45. http://dx.doi.org/10.20450/mjcce.2016.835.
Herraiz, Ana G., und Marcos G. Suero. „New Alkene Cyclopropanation Reactions Enabled by Photoredox Catalysis via Radical Carbenoids“. Synthesis 51, Nr. 14 (11.06.2019): 2821–28. http://dx.doi.org/10.1055/s-0037-1611872.
Altamore, Timothy M., Oanh T. K. Nguyen, Quentin I. Churches, Kate Cavanagh, Xuan T. T. Nguyen, Sandhya A. M. Duggan, Guy Y. Krippner und 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, Nr. 9 (2013): 1105. http://dx.doi.org/10.1071/ch13309.
Bilera, Igor V. „The Formation of Small Amounts of Cyclopropane during Pulsed Pyrolysis of C4–C5 Acyclic Alkanes in the Adiabatic Compression Reactor“. Reactions 4, Nr. 3 (19.07.2023): 381–97. http://dx.doi.org/10.3390/reactions4030023.
Zhuo, Chun-Xiang, und Jia-Le Wang. „Catalytic Deoxygenative Cyclopropanation of 1,2-Dicarbonyl or Monocarbonyl Compounds via Molybdenum Catalysis“. Synlett 33, Nr. 07 (13.11.2021): 599–608. http://dx.doi.org/10.1055/a-1696-4553.
Luo, Hui-Xin, You-Hong Niu, Xiao-Ping Cao und Xin-Shan Ye. „Cyclopropenes for the Synthesis of Cyclopropane-Fused Dihydroquinolines and Benzazepines“. Advanced Synthesis & Catalysis 357, Nr. 13 (10.09.2015): 2893–902. http://dx.doi.org/10.1002/adsc.201500203.
Hara, Koji, Edmond I. Eger, Michael J. Laster und R. Adron Harris. „Nonhalogenated Alkanes Cyclopropane and Butane Affect Neurotransmitter-gated Ion Channel and G-protein–coupled Receptors“. Anesthesiology 97, Nr. 6 (01.12.2002): 1512–20. http://dx.doi.org/10.1097/00000542-200212000-00025.
Liu, Yu, Qiao-Lin Wang, Zan Chen, Cong-Shan Zhou, Bi-Quan Xiong, Pan-Liang Zhang, Chang-An Yang und Quan Zhou. „Oxidative radical ring-opening/cyclization of cyclopropane derivatives“. Beilstein Journal of Organic Chemistry 15 (28.01.2019): 256–78. http://dx.doi.org/10.3762/bjoc.15.23.
Barkan, Daniel, Vivek Rao, George D. Sukenick und Michael S. Glickman. „Redundant Function of cmaA2 and mmaA2 in Mycobacterium tuberculosis cis Cyclopropanation of Oxygenated Mycolates“. Journal of Bacteriology 192, Nr. 14 (14.05.2010): 3661–68. http://dx.doi.org/10.1128/jb.00312-10.
Sathishkannan, Gopal, V. John Tamilarasan und Kannupal Srinivasan. „Nucleophilic ring-opening reactions of trans-2-aroyl-3-aryl-cyclopropane-1,1-dicarboxylates with hydrazines“. Organic & Biomolecular Chemistry 15, Nr. 6 (2017): 1400–1406. http://dx.doi.org/10.1039/c6ob02552h.
Jalkanen, K. J., J. D. Gale, G. J. Jalkanen, D. F. McIntosh, A. A. El-Azhary und G. M. Jensen. „trans-1,2-Dicyano-cyclopropane and other cyano-cyclopropane derivatives“. Theoretical Chemistry Accounts 119, Nr. 1-3 (17.10.2007): 211–29. http://dx.doi.org/10.1007/s00214-007-0391-6.
Freedman, Teresa B., Diane L. Hausch, Steven J. Cianciosi und 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, Nr. 6 (01.06.1998): 806–10. http://dx.doi.org/10.1139/v98-070.
Budynina, Ekaterina, Konstantin Ivanov, Ivan Sorokin und Mikhail Melnikov. „Ring Opening of Donor–Acceptor Cyclopropanes with N-Nucleophiles“. Synthesis 49, Nr. 14 (18.05.2017): 3035–68. http://dx.doi.org/10.1055/s-0036-1589021.
Wang, Lizhong, Zhenjie Su, Siran Qian, Weijian Ye und Cunde Wang. „Efficient Preparation of 2,3-Disubstituted Cyclopropane-1-Carbonitriles via Selective Decarboxylation of 1-Cyanocyclopropane-1-Carboxylates“. Journal of Chemical Research 41, Nr. 11 (November 2017): 636–40. http://dx.doi.org/10.3184/174751917x15094552081161.
Xie, Yaoming, und Henry F. Schaefer. „Aluminirene (HAlC2H2) and aluminirane (HAlC2H4): aluminum-substituted counterparts of cyclopropene and cyclopropane“. Journal of the American Chemical Society 112, Nr. 14 (Juli 1990): 5393–400. http://dx.doi.org/10.1021/ja00170a001.
Al Dulayymi, Ahmad R., und Mark S. Baird. „2-Vinyl-1,1,2-trihalocyclopropanes-valuable five carbon cyclopropane and cyclopropene synthetic intermediates“. Tetrahedron 52, Nr. 33 (August 1996): 10955–68. http://dx.doi.org/10.1016/0040-4020(96)00592-3.
DULAYYMI, A. R. A., J. R. A. DULAYYMI, M. S. BAIRD und G. KOZA. „ChemInform Abstract: Simple Four and Five Carbon Cyclopropane and Cyclopropene Synthetic Intermediates“. ChemInform 29, Nr. 44 (19.06.2010): no. http://dx.doi.org/10.1002/chin.199844321.