Zeitschriftenartikel zum Thema „Cycloalkanes“
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Herman, David C., Phillip M. Fedorak und J. William Costerton. „Biodegradation of cycloalkane carboxylic acids in oil sand tailings“. Canadian Journal of Microbiology 39, Nr. 6 (01.06.1993): 576–80. http://dx.doi.org/10.1139/m93-083.
Chen, Yubin, Bin Yuan, Chaomin Wang, Sihang Wang, Xianjun He, Caihong Wu, Xin Song et al. „Online measurements of cycloalkanes based on NO+ chemical ionization in proton transfer reaction time-of-flight mass spectrometry (PTR-ToF-MS)“. Atmospheric Measurement Techniques 15, Nr. 23 (02.12.2022): 6935–47. http://dx.doi.org/10.5194/amt-15-6935-2022.
Wang, Jian, He Liu, Shiguang Fan, Shuai Wang, Guanjun Xu, Aijun Guo und Zongxian Wang. „Dehydrogenation of Cycloalkanes over N-Doped Carbon-Supported Catalysts: The Effects of Active Component and Molecular Structure of the Substrate“. Nanomaterials 11, Nr. 11 (26.10.2021): 2846. http://dx.doi.org/10.3390/nano11112846.
Bogdanowicz-Szwed, Krystyna, und Michalina Kozicka. „Phase-Transfer Catalysed Alkylation of Enamines of some Cyclic β-Keto Carbothionic Acid Anilides with 1,2-Dibromoethane. Synthesis of Enamines of 1-Oxo-2-(3-phenyl tetrahydrothiazol-2-ylidene)-cycloalkanes“. Zeitschrift für Naturforschung B 42, Nr. 9 (01.09.1987): 1174–80. http://dx.doi.org/10.1515/znb-1987-0919.
Wang, Wei, Shaoying Sun, Fengan Han, Guangyi Li, Xianzhao Shao und Ning Li. „Synthesis of Diesel and Jet Fuel Range Cycloalkanes with Cyclopentanone and Furfural“. Catalysts 9, Nr. 11 (25.10.2019): 886. http://dx.doi.org/10.3390/catal9110886.
Staudt, Svenja, Edyta Burda, Carolin Giese, Christina A. Müller, Jan Marienhagen, Ulrich Schwaneberg, Werner Hummel, Karlheinz Drauz und Harald Gröger. „Direct Oxidation of Cycloalkanes to Cycloalkanones with Oxygen in Water“. Angewandte Chemie International Edition 52, Nr. 8 (21.01.2013): 2359–63. http://dx.doi.org/10.1002/anie.201204464.
Shen, Hai M., Xiong Wang, A. Bing Guo, Long Zhang und Yuan B. She. „Catalytic oxidation of cycloalkanes by porphyrin cobalt(II) through efficient utilization of oxidation intermediates“. Journal of Porphyrins and Phthalocyanines 24, Nr. 10 (29.09.2020): 1166–73. http://dx.doi.org/10.1142/s1088424620500303.
Silva, Letícia B., Felipe S. Stefanello, Sarah C. Feitosa, Clarissa P. Frizzo, Marcos A. P. Martins, Nilo Zanatta, Bernardo A. Iglesias und Helio G. Bonacorso. „Novel 7-(1H-pyrrol-1-yl)spiro[chromeno[4,3-b]quinoline-6,1′-cycloalkanes]: synthesis, cross-coupling reactions, and photophysical properties“. New Journal of Chemistry 45, Nr. 8 (2021): 4061–70. http://dx.doi.org/10.1039/d0nj05740a.
Wackett, Lawrence P. „Cycloalkanes and bacteria“. Environmental Microbiology 16, Nr. 1 (Januar 2014): 333–34. http://dx.doi.org/10.1111/1462-2920.12336.
Geraghty, Niall W. A., und John J. Hannan. „Functionalisation of cycloalkanes: the photomediated reaction of cycloalkanes with alkynes“. Tetrahedron Letters 42, Nr. 18 (April 2001): 3211–13. http://dx.doi.org/10.1016/s0040-4039(01)00390-2.
Xiu, Jianmin, und Wenbin Yi. „Radical-based regioselective cross-coupling of indoles and cycloalkanes“. Catalysis Science & Technology 6, Nr. 4 (2016): 998–1002. http://dx.doi.org/10.1039/c5cy01907a.
Fliszár, S., F. Poliquin, I. Bǎdilescu und E. Vauthier. „Structure dependent regularities of zero-point plus heat content energies in organic molecules“. Canadian Journal of Chemistry 66, Nr. 2 (01.02.1988): 300–303. http://dx.doi.org/10.1139/v88-052.
Nakayama, Kaii, Hidehiro Kamiya und Yohei Okada. „Radical cation Diels–Alder reactions of arylidene cycloalkanes“. Beilstein Journal of Organic Chemistry 18 (25.08.2022): 1100–1106. http://dx.doi.org/10.3762/bjoc.18.112.
Geraghty, Niall W. A., und John J. Hannan. „ChemInform Abstract: Functionalization of Cycloalkanes: The Photomediated Reaction of Cycloalkanes with Alkynes.“ ChemInform 32, Nr. 30 (25.05.2010): no. http://dx.doi.org/10.1002/chin.200130057.
Banerjee, Arghya, Satavisha Sarkar und Bhisma K. Patel. „C–H functionalisation of cycloalkanes“. Organic & Biomolecular Chemistry 15, Nr. 3 (2017): 505–30. http://dx.doi.org/10.1039/c6ob01975g.
Moir, Michael E., Stéphanie Charbonneau und J. Brian A. Mitchell. „SOOT REDUCTION CHEMICALS FOR IN-SITU BURNING“. International Oil Spill Conference Proceedings 1993, Nr. 1 (01.03.1993): 761–63. http://dx.doi.org/10.7901/2169-3358-1993-1-761.
Kögler, Gerhard, Hansotto Drotloff und Martin Möller. „Molecular Motion of Solid Cycloalkanes“. Molecular Crystals and Liquid Crystals Incorporating Nonlinear Optics 153, Nr. 1 (Dezember 1987): 179–89. http://dx.doi.org/10.1080/00268948708074534.
Wiberg, Kenneth B. „The C7−C10 Cycloalkanes Revisited“. Journal of Organic Chemistry 68, Nr. 24 (November 2003): 9322–29. http://dx.doi.org/10.1021/jo030227n.
Yonehara, Fumi, Yoshiyuki Kido, Satoshi Morita und Masahiko Yamaguchi. „GaCl3-Catalyzed Arylation of Cycloalkanes“. Journal of the American Chemical Society 123, Nr. 45 (November 2001): 11310–11. http://dx.doi.org/10.1021/ja0164172.
Kowert *, Bruce A., Jared B. Jones, Jacob A. Zahm und Robert M. Turner II. „Size-dependent diffusion in cycloalkanes“. Molecular Physics 102, Nr. 13 (10.07.2004): 1489–97. http://dx.doi.org/10.1080/00268970410001734251.
Wodrich, Matthew D., Jérôme F. Gonthier, Stephan N. Steinmann und Clémence Corminboeuf. „How Strained are Carbomeric-Cycloalkanes?“ Journal of Physical Chemistry A 114, Nr. 24 (24.06.2010): 6705–12. http://dx.doi.org/10.1021/jp1029322.
Drumright, R. E., E. Ellington, P. E. Kastl und D. B. Priddy. „Cycloalkane perketal initiators for styrene polymerization. 2. Decomposition chemistry of gem-bis(tert-butylperoxy)cycloalkanes“. Macromolecules 26, Nr. 9 (April 1993): 2253–58. http://dx.doi.org/10.1021/ma00061a018.
Letcher, T. M., J. D. Mercer-Chalmers, U. P. Govender und R. Battino. „Excess molar enthalpies and excess molar volumes of mixtures of cycloalkanes and pseudo-cycloalkanes“. Thermochimica Acta 224 (September 1993): 39–42. http://dx.doi.org/10.1016/0040-6031(93)80152-z.
Joudaki, Daryoush, und Fatemeh Shafiei. „QSPR Models for the Prediction of Some Thermodynamic Properties of Cycloalkanes Using GA-MLR Method“. Current Computer-Aided Drug Design 16, Nr. 5 (09.11.2020): 571–82. http://dx.doi.org/10.2174/1573409915666191028110756.
Chen, Fang, Ning Li, Shanshan Li, Guangyi Li, Aiqin Wang, Yu Cong, Xiaodong Wang und Tao Zhang. „Synthesis of jet fuel range cycloalkanes with diacetone alcohol from lignocellulose“. Green Chemistry 18, Nr. 21 (2016): 5751–55. http://dx.doi.org/10.1039/c6gc01497f.
Banerjee, Arghya, Sourav Kumar Santra, Aniket Mishra, Nilufa Khatun und Bhisma K. Patel. „Copper(i)-promoted cycloalkylation–peroxidation of unactivated alkenes via sp3C–H functionalisation“. Organic & Biomolecular Chemistry 13, Nr. 5 (2015): 1307–12. http://dx.doi.org/10.1039/c4ob01962h.
Zhang, Wanbo, Ping Guo, Xingbo Ge, Jianfen Du und Zhouhua Wang. „Influence factors on CO2 solubility in cycloalkanes and cycloalkane volume expansion: Temperature, pressure and molecular structure“. Journal of Molecular Liquids 332 (Juni 2021): 115859. http://dx.doi.org/10.1016/j.molliq.2021.115859.
Li, Zheng, Andrew L. Otsuki und Mark Mascal. „Production of cellulosic gasoline via levulinic ester self-condensation“. Green Chemistry 20, Nr. 16 (2018): 3804–8. http://dx.doi.org/10.1039/c8gc01432a.
Ansari, Istikhar A., Farasha Sama, Mukul Raizada, M. Shahid, Musheer Ahmad und Zafar A. Siddiqi. „Structurally well-characterized new multinuclear Cu(ii) and Zn(ii) clusters: X-ray crystallography, theoretical studies, and applications in catalysis“. New Journal of Chemistry 40, Nr. 11 (2016): 9840–52. http://dx.doi.org/10.1039/c6nj02150f.
Tang, Hao, Yancheng Hu, Guangyi Li, Aiqin Wang, Guoliang Xu, Cong Yu, Xiaodong Wang, Tao Zhang und Ning Li. „Synthesis of jet fuel range high-density polycycloalkanes with polycarbonate waste“. Green Chemistry 21, Nr. 14 (2019): 3789–95. http://dx.doi.org/10.1039/c9gc01627a.
Li, Ze-lin, Li-kun Jin und Chun Cai. „Efficient synthesis of 2-substituted azoles: radical C–H alkylation of azoles with dicumyl peroxide, methylarenes and cycloalkanes under metal-free condition“. Organic Chemistry Frontiers 4, Nr. 10 (2017): 2039–43. http://dx.doi.org/10.1039/c7qo00396j.
Yang, Qingjing, Pui Ying Choy, Yinuo Wu, Baomin Fan und Fuk Yee Kwong. „Oxidative coupling between C(sp2)–H and C(sp3)–H bonds of indoles and cyclic ethers/cycloalkanes“. Organic & Biomolecular Chemistry 14, Nr. 9 (2016): 2608–12. http://dx.doi.org/10.1039/c6ob00076b.
Kissin, Yury V. „Catagenesis of light cycloalkanes in petroleum“. Organic Geochemistry 15, Nr. 6 (Januar 1990): 575–94. http://dx.doi.org/10.1016/0146-6380(90)90103-7.
Drotloff, Hansotto, und Martin Möller. „On the phase transitions of cycloalkanes“. Thermochimica Acta 112, Nr. 1 (Februar 1987): 57–62. http://dx.doi.org/10.1016/0040-6031(87)88079-6.
Matsubara, Hiroshi, Yoshiko Hino, Masashi Tokizane und Ilhyong Ryu. „Microflow photo-radical chlorination of cycloalkanes“. Chemical Engineering Journal 167, Nr. 2-3 (März 2011): 567–71. http://dx.doi.org/10.1016/j.cej.2010.08.086.
Chatterjee, Basujit, Deepti Kalsi, Akash Kaithal, Alexis Bordet, Walter Leitner und Chidambaram Gunanathan. „One-pot dual catalysis for the hydrogenation of heteroarenes and arenes“. Catalysis Science & Technology 10, Nr. 15 (2020): 5163–70. http://dx.doi.org/10.1039/d0cy00928h.
Zhang, Xuesong, Hanwu Lei, Lei Zhu, Joan Wu und Shulin Chen. „From lignocellulosic biomass to renewable cycloalkanes for jet fuels“. Green Chemistry 17, Nr. 10 (2015): 4736–47. http://dx.doi.org/10.1039/c5gc01583a.
Nishimura, Norio, Tohru Tanaka und Takushi Motoyama. „Additivity of the partial molar volumes of organic compounds“. Canadian Journal of Chemistry 65, Nr. 9 (01.09.1987): 2248–53. http://dx.doi.org/10.1139/v87-375.
Ren, Guangzhi, Guangyi Li, Ying Zhang, Aiqin Wang, Xiaodong Wang, Yu Cong, Tao Zhang und Ning Li. „Synthesis of jet fuel and diesel range cycloalkanes with 2-methylfuran and benzaldehyde“. Sustainable Energy & Fuels 6, Nr. 4 (2022): 1156–63. http://dx.doi.org/10.1039/d1se01752g.
Zhang, Xuesong, Hanwu Lei, Lei Zhu, Moriko Qian, J. C. Chan, Xiaolu Zhu, Yupeng Liu et al. „Development of a catalytically green route from diverse lignocellulosic biomasses to high-density cycloalkanes for jet fuels“. Catalysis Science & Technology 6, Nr. 12 (2016): 4210–20. http://dx.doi.org/10.1039/c5cy01623a.
Tavanti, Michele, Juan Mangas-Sanchez, Sarah L. Montgomery, Matthew P. Thompson und Nicholas J. Turner. „A biocatalytic cascade for the amination of unfunctionalised cycloalkanes“. Organic & Biomolecular Chemistry 15, Nr. 46 (2017): 9790–93. http://dx.doi.org/10.1039/c7ob02569f.
Gutman, Ivan, und Haruo Hosoya. „Molecular Graphs with Equal Z-Counting and Independence Polynomials“. Zeitschrift für Naturforschung A 45, Nr. 5 (01.05.1990): 645–48. http://dx.doi.org/10.1515/zna-1990-0509.
Banerjee, Arghya, Sourav Kumar Santra, Nilufa Khatun, Wajid Ali und Bhisma K. Patel. „Oxidant controlled regioselective mono- and di-functionalization reactions of coumarins“. Chemical Communications 51, Nr. 84 (2015): 15422–25. http://dx.doi.org/10.1039/c5cc06200d.
Oswal, S. L., und M. M. Maisuria. „Speeds of sound, isentropic compressibilities, and excess molar volumes of cycloalkane, alkanes and aromatic hydrocarbons at 303.15 K. I. Results for cycloalkane + cycloalkanes, and cycloalkane + alkanes“. Journal of Molecular Liquids 100, Nr. 2 (Juli 2002): 91–112. http://dx.doi.org/10.1016/s0167-7322(02)00021-1.
Tang, Hao, Ning Li, Guangyi Li, Aiqin Wang, Yu Cong, Guoliang Xu, Xiaodong Wang und Tao Zhang. „Synthesis of gasoline and jet fuel range cycloalkanes and aromatics from poly(ethylene terephthalate) waste“. Green Chemistry 21, Nr. 10 (2019): 2709–19. http://dx.doi.org/10.1039/c9gc00571d.
Giustra, Zachary X., Gang Chen, Monica Vasiliu, Abhijeet Karkamkar, Tom Autrey, David A. Dixon und Shih-Yuan Liu. „A comparison of hydrogen release kinetics from 5- and 6-membered 1,2-BN-cycloalkanes“. RSC Advances 11, Nr. 54 (2021): 34132–36. http://dx.doi.org/10.1039/d1ra07477f.
Fang, Zhongxue, Chenlong Wei, Jing Lin, Zhenhua Liu, Wei Wang, Chenshu Xu, Xuemin Wang und Yu Wang. „Silver-catalyzed decarboxylative C(sp2)–C(sp3) coupling reactions via a radical mechanism“. Organic & Biomolecular Chemistry 15, Nr. 47 (2017): 9974–78. http://dx.doi.org/10.1039/c7ob02455j.
Yang, Xiaokun, Teng Li, Kan Tang, Xinpei Zhou, Mi Lu, Whalmany L. Ounkham, Stephen M. Spain, Brian J. Frost und Hongfei Lin. „Highly efficient conversion of terpenoid biomass to jet-fuel range cycloalkanes in a biphasic tandem catalytic process“. Green Chemistry 19, Nr. 15 (2017): 3566–73. http://dx.doi.org/10.1039/c7gc00710h.
Kirillova, Marina V., Polyana Tomé de Paiva, Wagner A. Carvalho, Dalmo Mandelli und Alexander M. Kirillov. „Mixed-ligand aminoalcohol-dicarboxylate copper(II) coordination polymers as catalysts for the oxidative functionalization of cyclic alkanes and alkenes“. Pure and Applied Chemistry 89, Nr. 1 (01.01.2017): 61–73. http://dx.doi.org/10.1515/pac-2016-1012.
Kong, Jiechen, Bolong Li und Chen Zhao. „Tuning Ni nanoparticles and the acid sites of silica-alumina for liquefaction and hydrodeoxygenation of lignin to cyclic alkanes“. RSC Advances 6, Nr. 76 (2016): 71940–51. http://dx.doi.org/10.1039/c6ra16977e.