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Journal articles on the topic 'Mild conditions'

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Author: Grafiati

Published: 22 June 2024

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1

Billet, R. "Rectification under Mild Conditions." Fett Wissenschaft Technologie/Fat Science Technology 89, no. 9 (1987): 362–68. http://dx.doi.org/10.1002/lipi.19870890909.

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2

DAGANI, RON. "FAST WORK UNDER MILD CONDITIONS." Chemical & Engineering News 79, no. 10 (March 5, 2001): 11. http://dx.doi.org/10.1021/cen-v079n010.p011a.

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3

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, no. 1 (January 23, 2008): 313–22. http://dx.doi.org/10.1002/prot.21927.

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4

Beck, Christopher M., Scott E. Rathmill, You Jung Park, Junyi Chen, Robert H. Crabtree, Louise M. Liable-Sands, and Arnold L. Rheingold. "Aldehyde Decarbonylation Catalysis under Mild Conditions." Organometallics 18, no. 25 (December 1999): 5311–17. http://dx.doi.org/10.1021/om9905106.

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5

Ma, Hongzhu, Xue Cui, Bo Wang, and Hongwei Chen. "Polymerization ofn-Heptane under Mild Conditions." Energy & Fuels 21, no. 4 (July 2007): 2473–74. http://dx.doi.org/10.1021/ef0701539.

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6

Müller, Annerose, Ulrich Roth, and Ralf Miethchen. "Balz-Schiemann decomposition under mild conditions." Journal of Fluorine Chemistry 29, no. 1-2 (August 1985): 205. http://dx.doi.org/10.1016/s0022-1139(00)83441-7.

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7

Fraenkel, Dan, Vivek R. Pradhan, John W. Tierney, and Irving Wender. "Liquefaction of coal under mild conditions." Fuel 70, no. 1 (January 1991): 64–73. http://dx.doi.org/10.1016/0016-2361(91)90096-s.

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8

Sultane, Prakash R., Trimbak B. Mete, and Ramakrishna G. Bhat. "Chemoselective N-deacetylation under mild conditions." Org. Biomol. Chem. 12, no. 2 (2014): 261–64. http://dx.doi.org/10.1039/c3ob41971a.

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9

Alvero, R., I. Carrizosa, J. A. Odriozola, and J. M. Trillo. "Hydration of Sm2O3 under mild conditions." Journal of the Less Common Metals 109, no. 2 (July 1985): 197–207. http://dx.doi.org/10.1016/0022-5088(85)90051-7.

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10

Dhara, Shubhendu, and Charles E. Diesendruck. "Olefination ofN-Sulfinylimines under Mild Conditions." European Journal of Organic Chemistry 2017, no. 8 (February 24, 2017): 1184–90. http://dx.doi.org/10.1002/ejoc.201601577.

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11

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, no. 6 (2022): 1600–1607. http://dx.doi.org/10.1039/d1sc05772c.

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A mild glycosylation system was developed using glycosyl imidate donors and a charge-enhanced thiourea H-bond donor catalyst. The method can be used for the effective synthesis of O-, C-, S- and N-glycosides and chemoselective one-pot glycosylation.

12

Yokota, Masaaki, Norihito Doki, and Hiroyuki Akagaki. "Solventless Organic Reactive Crystallization at Mild Conditions." Advances in Chemical Engineering and Science 05, no. 04 (2015): 461–64. http://dx.doi.org/10.4236/aces.2015.54047.

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13

Virot, Matthieu, Tony Chave, Denis Horlait, Nicolas Clavier, Nicolas Dacheux, Johann Ravaux, and Sergey I. Nikitenko. "Catalytic dissolution of ceria under mild conditions." Journal of Materials Chemistry 22, no. 29 (2012): 14734. http://dx.doi.org/10.1039/c2jm31996a.

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14

Kuninobu, Yoichiro, Hirokazu Ueda, Atsushi Kawata, and Kazuhiko Takai. "Rearrangement of Indene Skeletons under Mild Conditions." Journal of Organic Chemistry 72, no. 18 (August 2007): 6749–52. http://dx.doi.org/10.1021/jo070537w.

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15

Lu, Gang, Jonathan E. Grossman, Joseph B. Lambert, Zhijun Xiao, and Dan Fu. "Silicate digestion with fructose under mild conditions." Green Chemistry 8, no. 6 (2006): 533. http://dx.doi.org/10.1039/b600378h.

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16

Liu, Fang, Mingfeng Wang, Zhiqiang Wang, and Xi Zhang. "Polymerized surface micelles formed under mild conditions." Chemical Communications, no. 15 (2006): 1610. http://dx.doi.org/10.1039/b600498a.

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17

Blaskovich, Mark A., and Michael Kahn. "Mild Conditions for Oxazolidin-5-one Formation." Synthesis 1998, no. 04 (April 1998): 379–80. http://dx.doi.org/10.1055/s-1998-4486.

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18

CALCAGNI, A., G. LUISI, G. LUCENTE, F. PINNEN, and D. ROSSI. "Cyclization under mild conditions of salicyloyl-dipeptides." International Journal of Peptide and Protein Research 36, no. 3 (January 12, 2009): 240–46. http://dx.doi.org/10.1111/j.1399-3011.1990.tb00974.x.

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19

KATSUKI, Kazuko, and Yukichi YOSHINO. "Hydrothermal preparation of ultramarine under mild conditions." NIPPON KAGAKU KAISHI, no. 3 (1989): 364–67. http://dx.doi.org/10.1246/nikkashi.1989.364.

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20

Namba, Kosuke, Kohei Takeuchi, Atsushi Nakayama, and Keiji Tanino. "Facile Guanidine Formation under Mild Acidic Conditions." Synlett 27, no. 18 (August 1, 2016): 2591–96. http://dx.doi.org/10.1055/s-0035-1562478.

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21

Sitohy, Mahmoud, Jean-Marc Chobert, and Thomas Haertle. "Phosphorylation of .beta.-Lactoglobulin under Mild Conditions." Journal of Agricultural and Food Chemistry 43, no. 1 (January 1995): 59–62. http://dx.doi.org/10.1021/jf00049a012.

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22

Sadownik, Andrzej, James Stefely, and Steven L. Regen. "Polymerized liposomes formed under extremely mild conditions." Journal of the American Chemical Society 108, no. 24 (November 1986): 7789–91. http://dx.doi.org/10.1021/ja00284a050.

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23

Abel, Stephan, Torsten Linker, and Bernd Giese. "Ring Opening ofC-Glycosides under Mild Conditions." Synlett 1991, no. 03 (1991): 171–72. http://dx.doi.org/10.1055/s-1991-20666.

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24

Huang, Yujie, Yan Tang, Jun Wang, and Qianwang Chen. "Synthesis of MgFe2O4 nanocrystallites under mild conditions." Materials Chemistry and Physics 97, no. 2-3 (June 2006): 394–97. http://dx.doi.org/10.1016/j.matchemphys.2005.08.035.

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25

Lindsey, Jonathan S., Henry C. Hsu, and Irwin C. Schreiman. "Synthesis of tetraphenylporphyrins under very mild conditions." Tetrahedron Letters 27, no. 41 (January 1986): 4969–70. http://dx.doi.org/10.1016/s0040-4039(00)85109-6.

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26

Borisov, D. N., L. E. Foss, K. V. Shabalin, L. I. Musin, and R. Z. Musin. "Oxidative Cleavage of Asphaltenes Under Mild Conditions." Chemistry and Technology of Fuels and Oils 55, no. 5 (November 2019): 552–56. http://dx.doi.org/10.1007/s10553-019-01065-x.

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27

Tamura, Hiroshi, Hideaki Nagahama, and Seiichi Tokura. "Preparation of Chitin Hydrogel Under Mild Conditions." Cellulose 13, no. 4 (June 1, 2006): 357–64. http://dx.doi.org/10.1007/s10570-006-9058-z.

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28

El-Sheikh, Manal A. "Carboxymethylation of maize starch at mild conditions." Carbohydrate Polymers 79, no. 4 (March 17, 2010): 875–81. http://dx.doi.org/10.1016/j.carbpol.2009.10.013.

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29

Krishnan, Ranganathan, and Anbanandam Parthiban. "A multifunctionalization of octafluorocyclopentene under mild conditions." European Polymer Journal 101 (April 2018): 66–76. http://dx.doi.org/10.1016/j.eurpolymj.2018.01.024.

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30

Wang, Yali, Hong Zhang, and Wolfgang Voelter. "Block Synthesis of Oligosaccharides under Mild Conditions." Zeitschrift für Naturforschung B 50, no. 4 (April 1, 1995): 661–66. http://dx.doi.org/10.1515/znb-1995-0431.

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Abstract:

Details on a synthesis of the trisaccharide α-D-Glc(1→6)-β-D-Glc(1→6)-D -Glc are reported. The O-glycosidic linkages were constructed using the sulfoxide glycosylation reaction. This approach proves to be a rapid glycosylation method leading to high yield and good selectivity.

31

Schrock, Richard R. "Catalytic reduction of dinitrogen under mild conditions." Chemical Communications, no. 19 (2003): 2389. http://dx.doi.org/10.1039/b307784p.

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32

Langa, Fernando, Frédéric Oswald, and Pilar de la Cruz. "Nitration of Fullerene Derivatives under Mild Conditions." Synlett 2007, no. 7 (April 2007): 1051–54. http://dx.doi.org/10.1055/s-2007-977425.

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33

Kazanci, A., O. Y. Saribiyik, and S. Serin. "Mild Conditions for Oxidation/Epoxidation of Styrene." Designed Monomers and Polymers 14, no. 6 (January 1, 2011): 559–70. http://dx.doi.org/10.1163/156855511x598641.

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34

Ezquerro, J. A., and M. A. Hernández. "The Ulm method under mild differentiability conditions." Numerische Mathematik 109, no. 2 (February 15, 2008): 193–207. http://dx.doi.org/10.1007/s00211-008-0144-z.

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35

Cheprakov, A. V., D. I. Makhon'kov, and I. P. Beletskaya. "Oxidative bromination of adamantane under mild conditions." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 36, no. 3 (March 1987): 637. http://dx.doi.org/10.1007/bf00955868.

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36

Galloway, Jordan D., Cristian Sarabia, James C. Fettinger, Hrant P. Hratchian, and Ryan D. Baxter. "Versatile New Reagent for Nitrosation under Mild Conditions." Organic Letters 23, no. 9 (April 12, 2021): 3253–58. http://dx.doi.org/10.1021/acs.orglett.1c00637.

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37

Shi, Yijun, Xuejing Liu, Han Cao, Fusheng Bie, Ying Han, Peng Yan, Roman Szostak, Michal Szostak, and Chengwei Liu. "Conversion of esters to thioesters under mild conditions." Organic & Biomolecular Chemistry 19, no. 13 (2021): 2991–96. http://dx.doi.org/10.1039/d1ob00187f.

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38

Szpara, Rachel, Alexander Goyder, Michael J. Porter, Helen C. Hailes, and Tom D. Sheppard. "Regioselective Dehydration of Sugar Thioacetals under Mild Conditions." Organic Letters 23, no. 7 (March 17, 2021): 2488–92. http://dx.doi.org/10.1021/acs.orglett.1c00424.

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39

Petri, J. L., G. Berenhauser Leite, and G. L. Putti. "APPLE TREE BUDBREAK PROMOTERS IN MILD WINTER CONDITIONS." Acta Horticulturae, no. 774 (October 2008): 291–96. http://dx.doi.org/10.17660/actahortic.2008.774.39.

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40

Zolfigol, Mohammad, Ezat Ghaemi, and Elahe Madrakian. "Nitration Of Phenols Under Mild And Heterogeneous Conditions." Molecules 6, no. 7 (June 30, 2001): 614–20. http://dx.doi.org/10.3390/60700614.

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41

Shi, Wen-Juan, Xiao-Lei Li, Zhao-Wei Li, and Zhang-Jie Shi. "Nickel catalyzed reduction of arenols under mild conditions." Organic Chemistry Frontiers 3, no. 3 (2016): 375–79. http://dx.doi.org/10.1039/c5qo00395d.

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42

Frese, Karl W. "Partial electrochemical oxidation of methane under mild conditions." Langmuir 7, no. 1 (January 1991): 13–15. http://dx.doi.org/10.1021/la00049a004.

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43

Kalinina, Irina, and François Mathey. "Generating Phosphinidene−N-Methylimidazole Adducts under Mild Conditions." Organometallics 25, no. 21 (October 2006): 5031–34. http://dx.doi.org/10.1021/om060460m.

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44

Rajasingh, Paramasivan, Revital Cohen, Elijah Shirman, Linda J. W. Shimon, and Boris Rybtchinski. "Selective Bromination of Perylene Diimides under Mild Conditions." Journal of Organic Chemistry 72, no. 16 (August 2007): 5973–79. http://dx.doi.org/10.1021/jo070367n.

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45

Thallapally, Praveen K., Gareth O. Lloyd, Trevor B. Wirsig, Martin W. Bredenkamp, Jerry L. Atwood, and Leonard J. Barbour. "Organic crystals absorb hydrogen gas under mild conditions." Chemical Communications, no. 42 (2005): 5272. http://dx.doi.org/10.1039/b511341e.

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46

Finkelmeier, Nils, Arne Visscher, Sebastian Wandtke, Regine Herbst-Irmer, and Dietmar Stalke. "CH3-deprotonation of 9-methylanthracene under mild conditions." Chemical Communications 52, no. 31 (2016): 5440–42. http://dx.doi.org/10.1039/c6cc01261b.

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47

Luo, Jun, Yifei Ling, Pingping Zhang, Lu Sun, and Weipeng Lai. "Efficient Synthesis of 2,2,4,4,6,6-Hexanitroadamantane under Mild Conditions." Synthesis 46, no. 16 (May 13, 2014): 2225–33. http://dx.doi.org/10.1055/s-0033-1341251.

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48

Peng, C. J., X. H. Peng, H. M. Li, Y. Rong, X. Z. Dong, and Y. F. Tai. "Efficient Synthesis of Benzoylformic Acid Under Mild Conditions." Asian Journal of Chemistry 27, no. 1 (2015): 78–80. http://dx.doi.org/10.14233/ajchem.2015.16715.

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49

Shono, Atsushi, Takanori Hashimoto, Shinya Hodoshima, Kazumi Satoh, and Yasukazu Saito. "Continuous Catalytic Dehydrogenation of Decalin under Mild Conditions." JOURNAL OF CHEMICAL ENGINEERING OF JAPAN 39, no. 2 (2006): 211–15. http://dx.doi.org/10.1252/jcej.39.211.

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50

Li, Jia, Wenhao Bao, Zhaocheng Tang, Baodang Guo, Shiwei Zhang, Haili Liu, Shuping Huang, Yan Zhang, and Yijian Rao. "Cercosporin-bioinspired selective photooxidation reactions under mild conditions." Green Chemistry 21, no. 22 (2019): 6073–81. http://dx.doi.org/10.1039/c9gc02270h.

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