Статті в журналах з теми "Chemoselective Transformation"
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Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Chemoselective Transformation".
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Luo, Renshi, Yanping Xia, Lu Ouyang, Jianhua Liao та Xiao Yang. "Chemoselective Transfer Hydrogenation of α,β-Unsaturated Ketones Catalyzed by Iridium Complexes". SynOpen 05, № 01 (січень 2021): 36–42. http://dx.doi.org/10.1055/s-0040-1706022.
Повний текст джерелаTrader, Darci J., and Erin E. Carlson. "Chemoselective hydroxyl group transformation: an elusive target." Molecular BioSystems 8, no. 10 (2012): 2484. http://dx.doi.org/10.1039/c2mb25122a.
Повний текст джерелаWójtowicz-Rajchel, Hanna, and Marcin Kaźmierczak. "Chemo-, regio-, and stereoselectivity in 1,3-dipolar cycloaddition of piperine with nitrones. A cycloadditive route to aminoalcohols." New Journal of Chemistry 44, no. 15 (2020): 6015–25. http://dx.doi.org/10.1039/c9nj06442g.
Повний текст джерелаYu, Sifan, Jinzhou Chen, Gengxin Liu, Jinping Lei, Wenhao Hu та Huang Qiu. "A gold(i)-catalysed chemoselective three-component reaction between phenols, α-diazocarbonyl compounds and allenamides". Chemical Communications 56, № 11 (2020): 1649–52. http://dx.doi.org/10.1039/c9cc09470a.
Повний текст джерелаKuila, Bilash, Yogesh Kumar, Dinesh Mahajan, Kapil Kumar, Prabhpreet Singh, and Gaurav Bhargava. "A facile and chemoselective synthesis of 1,4-benzodiazepin-2-ones and dienyl thiazolidin-4-ones." RSC Advances 6, no. 62 (2016): 57485–89. http://dx.doi.org/10.1039/c6ra10021j.
Повний текст джерелаPanwar, Rahul, Shally Shally, Ranjay Shaw, Amr Elagamy, and Ramendra Pratap. "Chemoselective synthesis of m-teraryls through ring transformation of 2H-pyran-2-ones by 2-(1-arylethylidene)-malononitriles." Organic & Biomolecular Chemistry 16, no. 46 (2018): 8994–9002. http://dx.doi.org/10.1039/c8ob02370k.
Повний текст джерелаMa, Haojie, Xiaoqiang Zhou, Zhenzhen Zhan, Daidong Wei, Chong Shi, Xingxing Liu, and Guosheng Huang. "Copper-catalyzed transformation of ketones to amides via C(CO)–C(alkyl) bond cleavage directed by picolinamide." Organic & Biomolecular Chemistry 15, no. 35 (2017): 7365–68. http://dx.doi.org/10.1039/c7ob01636k.
Повний текст джерелаLaulhé, Sébastien, Sadakatali S. Gori, and Michael H. Nantz. "A Chemoselective, One-Pot Transformation of Aldehydes to Nitriles." Journal of Organic Chemistry 77, no. 20 (October 10, 2012): 9334–37. http://dx.doi.org/10.1021/jo301133y.
Повний текст джерелаBergueiro, Julián, Javier Montenegro, Carlos Saá, and Susana López. "One-step chemoselective conversion of tetrahydropyranyl ethers to silyl-protected alcohols." RSC Adv. 4, no. 28 (2014): 14475–79. http://dx.doi.org/10.1039/c4ra00655k.
Повний текст джерелаWang, Dawei, Yanwei Zhang, Rong Cai, and Xiaodong Shi. "Triazole–Au(I) complex as chemoselective catalyst in promoting propargyl ester rearrangements." Beilstein Journal of Organic Chemistry 7 (July 25, 2011): 1014–20. http://dx.doi.org/10.3762/bjoc.7.115.
Повний текст джерелаAlizadeh, Abdolali, Behnaz Farajpour та Mojtaba Khanpour. "Efficient Synthesis of 7,8-Dihydro-6H-benzo[c]chromen-6-one Derivatives by Base-Mediated Chemoselective Annulation of Alkylidene Malononitriles with α,β-Unsaturated Coumarins". Synlett 32, № 07 (22 січня 2021): 697–700. http://dx.doi.org/10.1055/s-0040-1706012.
Повний текст джерелаLaulhe, Sebastien, Sadakatali S. Gori, and Michael H. Nantz. "ChemInform Abstract: A Chemoselective, One-Pot Transformation of Aldehydes to Nitriles." ChemInform 44, no. 6 (February 5, 2013): no. http://dx.doi.org/10.1002/chin.201306037.
Повний текст джерелаSahoo, Santosh K., Nilufa Khatun, Anupal Gogoi, Arghya Deb, and Bhisma K. Patel. "Cu(ii) catalysed chemoselective oxidative transformation of thiourea to thioamidoguanidine/2-aminobenzothiazole." RSC Adv. 3, no. 2 (2013): 438–46. http://dx.doi.org/10.1039/c2ra22240j.
Повний текст джерелаGeng, Hui, and Pei-Qiang Huang. "Versatile and chemoselective transformation of aliphatic and aromatic secondary amides to nitriles." Tetrahedron 71, no. 23 (June 2015): 3795–801. http://dx.doi.org/10.1016/j.tet.2015.03.094.
Повний текст джерелаWang, Xing, Rui-Xi Chen, Zeng-Feng Wei, Chen-Yang Zhang, Hai-Yang Tu, and Ai-Dong Zhang. "Chemoselective Transformation of Diarylethanones to Arylmethanoic Acids and Diarylmethanones and Mechanistic Insights." Journal of Organic Chemistry 81, no. 1 (December 15, 2015): 238–49. http://dx.doi.org/10.1021/acs.joc.5b02506.
Повний текст джерелаChen, Hang, Jian-Liang Ye та Pei-Qiang Huang. "Chemoselective direct reductive trifluoromethylation of amides: a flexible access to functionalized α-trifluoromethylamines". Organic Chemistry Frontiers 5, № 6 (2018): 943–47. http://dx.doi.org/10.1039/c7qo01031a.
Повний текст джерелаSuárez-Castillo, Oscar R., Manuel García-Velgara, Martha S. Morales-Ríos, and Pedro Joseph-Nathan. "Chemoselective intramolecular annulation of 3-alkylindolines into dihydro or tetrahydrofuro[2,3-b]indoles." Canadian Journal of Chemistry 75, no. 7 (July 1, 1997): 959–64. http://dx.doi.org/10.1139/v97-115.
Повний текст джерелаLegault, Claude, Robin Dagenais, and Antoine Lauriers. "Iodine(III)-Mediated Oxidative Hydrolysis of Haloalkenes: Investigation of the Effect of Iodine(III) Reagents." Synthesis 49, no. 13 (June 7, 2017): 2928–32. http://dx.doi.org/10.1055/s-0036-1588439.
Повний текст джерелаSalgado, Mateo M., Alejandro Manchado, Carlos T. Nieto, David Díez, and Narciso M. Garrido. "Asymmetric Synthesis of 2,3,6-Trisubstituted Piperidines via Baylis–Hillman Adducts and Lithium Amide through Domino Reaction." Synlett 31, no. 06 (September 24, 2019): 600–604. http://dx.doi.org/10.1055/s-0039-1690990.
Повний текст джерелаVallée, M. Robert J., Paul Majkut, Ina Wilkening, Christoph Weise, Gregor Müller, and Christian P. R. Hackenberger. "Staudinger-Phosphonite Reactions for the Chemoselective Transformation of Azido-Containing Peptides and Proteins." Organic Letters 13, no. 20 (October 21, 2011): 5440–43. http://dx.doi.org/10.1021/ol2020175.
Повний текст джерелаJiang, X., K. Kulbitski, G. Nisnevich, and M. Gandelman. "Enantioselective assembly of tertiary stereocenters via multicomponent chemoselective cross-coupling of geminal chloro(iodo)alkanes." Chemical Science 7, no. 4 (2016): 2762–67. http://dx.doi.org/10.1039/c5sc04378f.
Повний текст джерелаSuzuki, Takeshi, and Takeshi Oriyama. "A Novel and Chemoselective Transformation of Alcohol Silyl Ethers into the Corresponding Tetrahydropyranyl Ethers." Synthesis 2001, no. 04 (2001): 0555–58. http://dx.doi.org/10.1055/s-2001-12343.
Повний текст джерелаGeng, Hui, and Pei-Qiang Huang. "ChemInform Abstract: Versatile and Chemoselective Transformation of Aliphatic and Aromatic Secondary Amides to Nitriles." ChemInform 46, no. 37 (August 27, 2015): no. http://dx.doi.org/10.1002/chin.201537050.
Повний текст джерелаSahoo, Santosh K., Nilufa Khatun, Anupal Gogoi, Arghya Deb, and Bhismar K. Patel. "ChemInform Abstract: Cu(II) Catalyzed Chemoselective Oxidative Transformation of Thiourea to Thioamidoguanidine/2-Aminobenzothiazole." ChemInform 44, no. 21 (May 2, 2013): no. http://dx.doi.org/10.1002/chin.201321148.
Повний текст джерелаHuo, Zhibao, Jiefeng Xiao, Dezhang Ren, Fangming Jin, Tian Wang, and Guodong Yao. "Chemoselective synthesis of propionic acid from biomass and lactic acid over a cobalt catalyst in aqueous media." Green Chemistry 19, no. 5 (2017): 1308–14. http://dx.doi.org/10.1039/c6gc03036j.
Повний текст джерелаMcCullough, Richard D., and Shawn P. Williams. "A Dramatic Conformational Transformation of a Regioregular Polythiophene via a Chemoselective, Metal-Ion Assisted Deconjugation." Chemistry of Materials 7, no. 11 (November 1995): 2001–3. http://dx.doi.org/10.1021/cm00059a004.
Повний текст джерелаKotsuki, Hiyoshizo, Takeshi Ohishi, and Tomohiro Araki. "A new facile method for the chemoselective reductive transformation of azides to N-(tert-butoxycarbonyl)amines." Tetrahedron Letters 38, no. 12 (March 1997): 2129–32. http://dx.doi.org/10.1016/s0040-4039(97)00324-9.
Повний текст джерелаSuzuki, Takeshi, and Takeshi Oriyama. "ChemInform Abstract: A Novel and Chemoselective Transformation of Alcohol Silyl Ethers into the Corresponding Tetrahydropyranyl Ethers." ChemInform 32, no. 29 (May 25, 2010): no. http://dx.doi.org/10.1002/chin.200129076.
Повний текст джерелаAdair, Jennifer E., Christopher R. Burtner, and Hans-Peter Kiem. "Maintenance of Leukocyte Telomere Length after Transplant and Chemoselection in Macaques with Polyclonal Gene Modified Cell Engraftment." Blood 126, no. 23 (December 3, 2015): 3236. http://dx.doi.org/10.1182/blood.v126.23.3236.3236.
Повний текст джерелаLezina, Olga M., Svetlana N. Subbotina, Larisa L. Frolova, Svetlana A. Rubtsova та Denis V. Sudarikov. "Synthesis and Oxidative Transformations of New Chiral Pinane-Type γ-Ketothiols: Stereochemical Features of Reactions". Molecules 26, № 17 (29 серпня 2021): 5245. http://dx.doi.org/10.3390/molecules26175245.
Повний текст джерелаSakaitani, Masahiro, and Yasufumi Ohfune. "Syntheses and reactions of silyl carbamates. 1. Chemoselective transformation of amino protecting groups via tert-butyldimethylsilyl carbamates." Journal of Organic Chemistry 55, no. 3 (February 1990): 870–76. http://dx.doi.org/10.1021/jo00290a015.
Повний текст джерелаKenny, Niall P., Kamalraj V. Rajendran, and Declan G. Gilheany. "Chemoselective reduction of the phosphoryl bond of O-alkyl phosphinates and related compounds: an apparently impossible transformation." Chemical Communications 51, no. 92 (2015): 16561–64. http://dx.doi.org/10.1039/c5cc06389b.
Повний текст джерелаOkamoto, Akiko, Kazuhiro Kumeda, and Noriyuki Yonezawa. "AlCl3-mediated Defluorinative Diarylhydroxylation Transformation of CF3: Chemoselective Arylation of CF3and Chlorocarbonyl Groups Attached to Aromatic Rings." Chemistry Letters 39, no. 2 (February 5, 2010): 124–25. http://dx.doi.org/10.1246/cl.2010.124.
Повний текст джерелаKOTSUKI, H., T. OHISHI, and T. ARAKI. "ChemInform Abstract: A New Facile Method for the Chemoselective Reductive Transformation of Azides to N-(tert-Butoxycarbonyl)amines." ChemInform 28, no. 26 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199726077.
Повний текст джерелаKarthikeyan, Soundararajan, Radha Krishnan Shobana, Kamarajapurathu Raju Subimol, J. Helen Ratna Monica, and Ayyanoth Karthik Krishna Kumar. "Azidophosphonium salt-directed chemoselective synthesis of (E)/(Z)-cinnamyl-1H-triazoles and regiospecific access to bromomethylcoumarins from Morita–Baylis–Hillman adducts." Beilstein Journal of Organic Chemistry 16 (July 1, 2020): 1579–87. http://dx.doi.org/10.3762/bjoc.16.130.
Повний текст джерелаBew, Sean P., Glyn D. Hiatt-Gipson, Graham P. Mills, and Claire E. Reeves. "Efficient syntheses of climate relevant isoprene nitrates and (1R,5S)-(−)-myrtenol nitrate." Beilstein Journal of Organic Chemistry 12 (May 27, 2016): 1081–95. http://dx.doi.org/10.3762/bjoc.12.103.
Повний текст джерелаLeonelli, Francesca, Irene Piergentili, Giulio Lucarelli, Luisa Maria Migneco, and Rinaldo Marini Bettolo. "Unexpected Racemization in the Course of the Acetalization of (+)-(S)-5-Methyl-Wieland–Miescher Ketone with 1,2-Ethanediol and TsOH under Classical Experimental Conditions." International Journal of Molecular Sciences 20, no. 24 (December 5, 2019): 6147. http://dx.doi.org/10.3390/ijms20246147.
Повний текст джерелаOkamoto, Akiko, Kazuhiro Kumeda, and Noriyuki Yonezawa. "ChemInform Abstract: AlCl3-Mediated Defluorinative Diarylhydroxylation Transformation of CF3: Chemoselective Arylation of CF3 and Chlorocarbonyl Groups Attached to Aromatic Rings." ChemInform 41, no. 29 (June 24, 2010): no. http://dx.doi.org/10.1002/chin.201029101.
Повний текст джерелаDemeter, Fruzsina, Margaret Dah-Tsyr Chang, Yuan-Chuan Lee, Anikó Borbás, and Mihály Herczeg. "An Efficient Synthesis of the Pentasaccharide Repeating Unit of Pseudomonas aeruginosa Psl Exopolysaccharide." Synlett 31, no. 05 (November 19, 2019): 469–74. http://dx.doi.org/10.1055/s-0039-1690747.
Повний текст джерелаSong, Xixi, Xinshuai Zhang, Shilei Zhang, Hao Li, and Wei Wang. "Direct Transformation of Simple Enals to 3,4-Disubstituted Benzaldehydes under Mild Reaction Conditions via an Organocatalytic Regio- and Chemoselective Dimerization Cascade." Chemistry - A European Journal 18, no. 32 (June 28, 2012): 9770–74. http://dx.doi.org/10.1002/chem.201201709.
Повний текст джерелаSun, Xianwei, Zhenlei Song, Hongze Li та Changzheng Sun. "[1,4]‐S‐ to O‐Silyl Migration: Multicomponent Synthesis of α‐Thioketones through Chemoselective Transformation of Esters to Ketones with Organolithium Reagents". Chemistry – A European Journal 19, № 51 (14 листопада 2013): 17589–94. http://dx.doi.org/10.1002/chem.201303459.
Повний текст джерелаSun, Xianwei, Zhenlei Song, Hongze Li та Changzheng Sun. "ChemInform Abstract: [1,4]-S- to O-Silyl Migration: Multicomponent Synthesis of α-Thioketones Through Chemoselective Transformation of Esters to Ketones with Organolithium Reagents." ChemInform 45, № 21 (8 травня 2014): no. http://dx.doi.org/10.1002/chin.201421050.
Повний текст джерелаSong, Xixi, Xinshuai Zhang, Shilei Zhang, Hao Li, and Wei Wang. "ChemInform Abstract: Direct Transformation of Simple Enals to 3,4-Disubstituted Benzaldehydes under Mild Reaction Conditions via an Organocatalytic Regio- and Chemoselective Dimerization Cascade." ChemInform 44, no. 3 (January 15, 2013): no. http://dx.doi.org/10.1002/chin.201303031.
Повний текст джерелаKiss, Loránd, Márton Kardos, Csaba Vass та Ferenc Fülöp. "Application of Metathesis Reactions in the Synthesis and Transformations of Functionalized β-Amino Acid Derivatives". Synthesis 50, № 18 (26 липня 2018): 3571–88. http://dx.doi.org/10.1055/s-0036-1591600.
Повний текст джерелаShukla, Gaurav, Abhijeet Srivastava, Dhananjay Yadav, and Maya Shankar Singh. "Copper-Catalyzed One-Pot Cross-Dehydrogenative Thienannulation: Chemoselective Access to Naphtho[2,1-b]thiophene-4,5-diones and Subsequent Transformation to Benzo[a]thieno[3,2-c]phenazines." Journal of Organic Chemistry 83, no. 4 (January 26, 2018): 2173–81. http://dx.doi.org/10.1021/acs.joc.7b03092.
Повний текст джерелаDecker, David, Hans-Joachim Drexler, Detlef Heller, and Torsten Beweries. "Homogeneous catalytic transfer semihydrogenation of alkynes – an overview of hydrogen sources, catalysts and reaction mechanisms." Catalysis Science & Technology 10, no. 19 (2020): 6449–63. http://dx.doi.org/10.1039/d0cy01276a.
Повний текст джерелаMa, Yating, and Zhaohui Li. "Coupling plasmonic noble metal with TiO2 for efficient photocatalytic transfer hydrogenation: M/TiO2 (M = Au and Pt) for chemoselective transformation of cinnamaldehyde to cinnamyl alcohol under visible and 365 nm UV light." Applied Surface Science 452 (September 2018): 279–85. http://dx.doi.org/10.1016/j.apsusc.2018.04.244.
Повний текст джерелаKnochel, Paul, Andreas Boudier, Lars O. Bromm, Eike Hupe, Jesús A. Varela, Alain Rodriguez, Christopher Koradin, Tanasri Bunlaksananusorn, Hamid Laaziri, and Frédéric Lhermitte. "Selective transformations mediated by main-group organometallics." Pure and Applied Chemistry 72, no. 9 (January 1, 2000): 1699–703. http://dx.doi.org/10.1351/pac200072091699.
Повний текст джерелаNolan, Steven P., and Hervé Clavier. "Chemoselective olefin metathesis transformations mediated by ruthenium complexes." Chemical Society Reviews 39, no. 8 (2010): 3305. http://dx.doi.org/10.1039/b912410c.
Повний текст джерелаTani, Yosuke, Kazunari Kuga, Tetsuaki Fujihara, Jun Terao, and Yasushi Tsuji. "Copper-catalyzed C–C bond-forming transformation of CO2 to alcohol oxidation level: selective synthesis of homoallylic alcohols from allenes, CO2, and hydrosilanes." Chemical Communications 51, no. 65 (2015): 13020–23. http://dx.doi.org/10.1039/c5cc03932k.
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