Artigos de revistas sobre o tema "Mild conditions"
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Billet, R. "Rectification under Mild Conditions". Fett Wissenschaft Technologie/Fat Science Technology 89, n.º 9 (1987): 362–68. http://dx.doi.org/10.1002/lipi.19870890909.
DAGANI, RON. "FAST WORK UNDER MILD CONDITIONS". Chemical & Engineering News 79, n.º 10 (5 de março de 2001): 11. http://dx.doi.org/10.1021/cen-v079n010.p011a.
Nonaka, Yasuhiro, Tomoyasu Aizawa, Daisuke Akieda, Masanori Yasui, Masahiro Watanabe, Nobuhisa Watanabe, Isao Tanaka et al. "Spontaneous asparaginyl deamidation of canine milk lysozyme under mild conditions". Proteins: Structure, Function, and Bioinformatics 72, n.º 1 (23 de janeiro de 2008): 313–22. http://dx.doi.org/10.1002/prot.21927.
Beck, Christopher M., Scott E. Rathmill, You Jung Park, Junyi Chen, Robert H. Crabtree, Louise M. Liable-Sands e Arnold L. Rheingold. "Aldehyde Decarbonylation Catalysis under Mild Conditions". Organometallics 18, n.º 25 (dezembro de 1999): 5311–17. http://dx.doi.org/10.1021/om9905106.
Ma, Hongzhu, Xue Cui, Bo Wang e Hongwei Chen. "Polymerization ofn-Heptane under Mild Conditions". Energy & Fuels 21, n.º 4 (julho de 2007): 2473–74. http://dx.doi.org/10.1021/ef0701539.
Müller, Annerose, Ulrich Roth e Ralf Miethchen. "Balz-Schiemann decomposition under mild conditions". Journal of Fluorine Chemistry 29, n.º 1-2 (agosto de 1985): 205. http://dx.doi.org/10.1016/s0022-1139(00)83441-7.
Fraenkel, Dan, Vivek R. Pradhan, John W. Tierney e Irving Wender. "Liquefaction of coal under mild conditions". Fuel 70, n.º 1 (janeiro de 1991): 64–73. http://dx.doi.org/10.1016/0016-2361(91)90096-s.
Sultane, Prakash R., Trimbak B. Mete e Ramakrishna G. Bhat. "Chemoselective N-deacetylation under mild conditions". Org. Biomol. Chem. 12, n.º 2 (2014): 261–64. http://dx.doi.org/10.1039/c3ob41971a.
Alvero, R., I. Carrizosa, J. A. Odriozola e J. M. Trillo. "Hydration of Sm2O3 under mild conditions". Journal of the Less Common Metals 109, n.º 2 (julho de 1985): 197–207. http://dx.doi.org/10.1016/0022-5088(85)90051-7.
Dhara, Shubhendu, e Charles E. Diesendruck. "Olefination ofN-Sulfinylimines under Mild Conditions". European Journal of Organic Chemistry 2017, n.º 8 (24 de fevereiro de 2017): 1184–90. http://dx.doi.org/10.1002/ejoc.201601577.
Xiao, Ke, Yongxin Hu, Yongyong Wan, XinXin Li, Qin Nie, Hao Yan, Liming Wang et al. "Hydrogen bond activated glycosylation under mild conditions". Chemical Science 13, n.º 6 (2022): 1600–1607. http://dx.doi.org/10.1039/d1sc05772c.
Yokota, Masaaki, Norihito Doki e Hiroyuki Akagaki. "Solventless Organic Reactive Crystallization at Mild Conditions". Advances in Chemical Engineering and Science 05, n.º 04 (2015): 461–64. http://dx.doi.org/10.4236/aces.2015.54047.
Virot, Matthieu, Tony Chave, Denis Horlait, Nicolas Clavier, Nicolas Dacheux, Johann Ravaux e Sergey I. Nikitenko. "Catalytic dissolution of ceria under mild conditions". Journal of Materials Chemistry 22, n.º 29 (2012): 14734. http://dx.doi.org/10.1039/c2jm31996a.
Kuninobu, Yoichiro, Hirokazu Ueda, Atsushi Kawata e Kazuhiko Takai. "Rearrangement of Indene Skeletons under Mild Conditions". Journal of Organic Chemistry 72, n.º 18 (agosto de 2007): 6749–52. http://dx.doi.org/10.1021/jo070537w.
Lu, Gang, Jonathan E. Grossman, Joseph B. Lambert, Zhijun Xiao e Dan Fu. "Silicate digestion with fructose under mild conditions". Green Chemistry 8, n.º 6 (2006): 533. http://dx.doi.org/10.1039/b600378h.
Liu, Fang, Mingfeng Wang, Zhiqiang Wang e Xi Zhang. "Polymerized surface micelles formed under mild conditions". Chemical Communications, n.º 15 (2006): 1610. http://dx.doi.org/10.1039/b600498a.
Blaskovich, Mark A., e Michael Kahn. "Mild Conditions for Oxazolidin-5-one Formation". Synthesis 1998, n.º 04 (abril de 1998): 379–80. http://dx.doi.org/10.1055/s-1998-4486.
CALCAGNI, A., G. LUISI, G. LUCENTE, F. PINNEN e D. ROSSI. "Cyclization under mild conditions of salicyloyl-dipeptides". International Journal of Peptide and Protein Research 36, n.º 3 (12 de janeiro de 2009): 240–46. http://dx.doi.org/10.1111/j.1399-3011.1990.tb00974.x.
KATSUKI, Kazuko, e Yukichi YOSHINO. "Hydrothermal preparation of ultramarine under mild conditions." NIPPON KAGAKU KAISHI, n.º 3 (1989): 364–67. http://dx.doi.org/10.1246/nikkashi.1989.364.
Namba, Kosuke, Kohei Takeuchi, Atsushi Nakayama e Keiji Tanino. "Facile Guanidine Formation under Mild Acidic Conditions". Synlett 27, n.º 18 (1 de agosto de 2016): 2591–96. http://dx.doi.org/10.1055/s-0035-1562478.
Sitohy, Mahmoud, Jean-Marc Chobert e Thomas Haertle. "Phosphorylation of .beta.-Lactoglobulin under Mild Conditions". Journal of Agricultural and Food Chemistry 43, n.º 1 (janeiro de 1995): 59–62. http://dx.doi.org/10.1021/jf00049a012.
Sadownik, Andrzej, James Stefely e Steven L. Regen. "Polymerized liposomes formed under extremely mild conditions". Journal of the American Chemical Society 108, n.º 24 (novembro de 1986): 7789–91. http://dx.doi.org/10.1021/ja00284a050.
Abel, Stephan, Torsten Linker e Bernd Giese. "Ring Opening ofC-Glycosides under Mild Conditions". Synlett 1991, n.º 03 (1991): 171–72. http://dx.doi.org/10.1055/s-1991-20666.
Huang, Yujie, Yan Tang, Jun Wang e Qianwang Chen. "Synthesis of MgFe2O4 nanocrystallites under mild conditions". Materials Chemistry and Physics 97, n.º 2-3 (junho de 2006): 394–97. http://dx.doi.org/10.1016/j.matchemphys.2005.08.035.
Lindsey, Jonathan S., Henry C. Hsu e Irwin C. Schreiman. "Synthesis of tetraphenylporphyrins under very mild conditions". Tetrahedron Letters 27, n.º 41 (janeiro de 1986): 4969–70. http://dx.doi.org/10.1016/s0040-4039(00)85109-6.
Borisov, D. N., L. E. Foss, K. V. Shabalin, L. I. Musin e R. Z. Musin. "Oxidative Cleavage of Asphaltenes Under Mild Conditions". Chemistry and Technology of Fuels and Oils 55, n.º 5 (novembro de 2019): 552–56. http://dx.doi.org/10.1007/s10553-019-01065-x.
Tamura, Hiroshi, Hideaki Nagahama e Seiichi Tokura. "Preparation of Chitin Hydrogel Under Mild Conditions". Cellulose 13, n.º 4 (1 de junho de 2006): 357–64. http://dx.doi.org/10.1007/s10570-006-9058-z.
El-Sheikh, Manal A. "Carboxymethylation of maize starch at mild conditions". Carbohydrate Polymers 79, n.º 4 (17 de março de 2010): 875–81. http://dx.doi.org/10.1016/j.carbpol.2009.10.013.
Krishnan, Ranganathan, e Anbanandam Parthiban. "A multifunctionalization of octafluorocyclopentene under mild conditions". European Polymer Journal 101 (abril de 2018): 66–76. http://dx.doi.org/10.1016/j.eurpolymj.2018.01.024.
Wang, Yali, Hong Zhang e Wolfgang Voelter. "Block Synthesis of Oligosaccharides under Mild Conditions". Zeitschrift für Naturforschung B 50, n.º 4 (1 de abril de 1995): 661–66. http://dx.doi.org/10.1515/znb-1995-0431.
Schrock, Richard R. "Catalytic reduction of dinitrogen under mild conditions". Chemical Communications, n.º 19 (2003): 2389. http://dx.doi.org/10.1039/b307784p.
Langa, Fernando, Frédéric Oswald e Pilar de la Cruz. "Nitration of Fullerene Derivatives under Mild Conditions". Synlett 2007, n.º 7 (abril de 2007): 1051–54. http://dx.doi.org/10.1055/s-2007-977425.
Kazanci, A., O. Y. Saribiyik e S. Serin. "Mild Conditions for Oxidation/Epoxidation of Styrene". Designed Monomers and Polymers 14, n.º 6 (1 de janeiro de 2011): 559–70. http://dx.doi.org/10.1163/156855511x598641.
Ezquerro, J. A., e M. A. Hernández. "The Ulm method under mild differentiability conditions". Numerische Mathematik 109, n.º 2 (15 de fevereiro de 2008): 193–207. http://dx.doi.org/10.1007/s00211-008-0144-z.
Cheprakov, A. V., D. I. Makhon'kov e I. P. Beletskaya. "Oxidative bromination of adamantane under mild conditions". Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 36, n.º 3 (março de 1987): 637. http://dx.doi.org/10.1007/bf00955868.
Galloway, Jordan D., Cristian Sarabia, James C. Fettinger, Hrant P. Hratchian e Ryan D. Baxter. "Versatile New Reagent for Nitrosation under Mild Conditions". Organic Letters 23, n.º 9 (12 de abril de 2021): 3253–58. http://dx.doi.org/10.1021/acs.orglett.1c00637.
Shi, Yijun, Xuejing Liu, Han Cao, Fusheng Bie, Ying Han, Peng Yan, Roman Szostak, Michal Szostak e Chengwei Liu. "Conversion of esters to thioesters under mild conditions". Organic & Biomolecular Chemistry 19, n.º 13 (2021): 2991–96. http://dx.doi.org/10.1039/d1ob00187f.
Szpara, Rachel, Alexander Goyder, Michael J. Porter, Helen C. Hailes e Tom D. Sheppard. "Regioselective Dehydration of Sugar Thioacetals under Mild Conditions". Organic Letters 23, n.º 7 (17 de março de 2021): 2488–92. http://dx.doi.org/10.1021/acs.orglett.1c00424.
Petri, J. L., G. Berenhauser Leite e G. L. Putti. "APPLE TREE BUDBREAK PROMOTERS IN MILD WINTER CONDITIONS". Acta Horticulturae, n.º 774 (outubro de 2008): 291–96. http://dx.doi.org/10.17660/actahortic.2008.774.39.
Zolfigol, Mohammad, Ezat Ghaemi e Elahe Madrakian. "Nitration Of Phenols Under Mild And Heterogeneous Conditions". Molecules 6, n.º 7 (30 de junho de 2001): 614–20. http://dx.doi.org/10.3390/60700614.
Shi, Wen-Juan, Xiao-Lei Li, Zhao-Wei Li e Zhang-Jie Shi. "Nickel catalyzed reduction of arenols under mild conditions". Organic Chemistry Frontiers 3, n.º 3 (2016): 375–79. http://dx.doi.org/10.1039/c5qo00395d.
Frese, Karl W. "Partial electrochemical oxidation of methane under mild conditions". Langmuir 7, n.º 1 (janeiro de 1991): 13–15. http://dx.doi.org/10.1021/la00049a004.
Kalinina, Irina, e François Mathey. "Generating Phosphinidene−N-Methylimidazole Adducts under Mild Conditions". Organometallics 25, n.º 21 (outubro de 2006): 5031–34. http://dx.doi.org/10.1021/om060460m.
Rajasingh, Paramasivan, Revital Cohen, Elijah Shirman, Linda J. W. Shimon e Boris Rybtchinski. "Selective Bromination of Perylene Diimides under Mild Conditions". Journal of Organic Chemistry 72, n.º 16 (agosto de 2007): 5973–79. http://dx.doi.org/10.1021/jo070367n.
Thallapally, Praveen K., Gareth O. Lloyd, Trevor B. Wirsig, Martin W. Bredenkamp, Jerry L. Atwood e Leonard J. Barbour. "Organic crystals absorb hydrogen gas under mild conditions". Chemical Communications, n.º 42 (2005): 5272. http://dx.doi.org/10.1039/b511341e.
Finkelmeier, Nils, Arne Visscher, Sebastian Wandtke, Regine Herbst-Irmer e Dietmar Stalke. "CH3-deprotonation of 9-methylanthracene under mild conditions". Chemical Communications 52, n.º 31 (2016): 5440–42. http://dx.doi.org/10.1039/c6cc01261b.
Luo, Jun, Yifei Ling, Pingping Zhang, Lu Sun e Weipeng Lai. "Efficient Synthesis of 2,2,4,4,6,6-Hexanitroadamantane under Mild Conditions". Synthesis 46, n.º 16 (13 de maio de 2014): 2225–33. http://dx.doi.org/10.1055/s-0033-1341251.
Peng, C. J., X. H. Peng, H. M. Li, Y. Rong, X. Z. Dong e Y. F. Tai. "Efficient Synthesis of Benzoylformic Acid Under Mild Conditions". Asian Journal of Chemistry 27, n.º 1 (2015): 78–80. http://dx.doi.org/10.14233/ajchem.2015.16715.
Shono, Atsushi, Takanori Hashimoto, Shinya Hodoshima, Kazumi Satoh e Yasukazu Saito. "Continuous Catalytic Dehydrogenation of Decalin under Mild Conditions". JOURNAL OF CHEMICAL ENGINEERING OF JAPAN 39, n.º 2 (2006): 211–15. http://dx.doi.org/10.1252/jcej.39.211.
Li, Jia, Wenhao Bao, Zhaocheng Tang, Baodang Guo, Shiwei Zhang, Haili Liu, Shuping Huang, Yan Zhang e Yijian Rao. "Cercosporin-bioinspired selective photooxidation reactions under mild conditions". Green Chemistry 21, n.º 22 (2019): 6073–81. http://dx.doi.org/10.1039/c9gc02270h.