Статті в журналах з теми "Chiral solvating agents"
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Giordano, Claudio, and Angelo Restelli. "New chiral solvating agents: 1,5-Benzothiazepines." Tetrahedron: Asymmetry 2, no. 8 (January 1991): 785–88. http://dx.doi.org/10.1016/s0957-4166(00)80460-7.
Повний текст джерелаLi, Gao-Wei, Xiao-Juan Wang, Dan-Dan Cui, Yu-Fei Zhang, Rong-Yao Xu, Shuai-Hua Shi, Lan-Tao Liu, Min-Can Wang, Hong-Min Liu, and Xin-Xiang Lei. "Azaheterocyclic diphenylmethanol chiral solvating agents for the NMR chiral discrimination of alpha-substituted carboxylic acids." RSC Advances 10, no. 57 (2020): 34605–11. http://dx.doi.org/10.1039/d0ra06312f.
Повний текст джерелаFang, Lixia, Caixia Lv, Guo Wang, Lei Feng, Pericles Stavropoulos, Guangpeng Gao, Lin Ai, and Jiaxin Zhang. "Discrimination of enantiomers of dipeptide derivatives with two chiral centers by tetraaza macrocyclic chiral solvating agents using 1H NMR spectroscopy." Organic Chemistry Frontiers 3, no. 12 (2016): 1716–24. http://dx.doi.org/10.1039/c6qo00521g.
Повний текст джерелаZhang, Hanchang, Hongmei Zhao, Jie Wen, Zhanbin Zhang, Pericles Stavropoulos, Yanlin Li, Lin Ai, and Jiaxin Zhang. "Discrimination of enantiomers of amides with two stereogenic centers enabled by chiral bisthiourea derivatives using 1H NMR spectroscopy." Organic & Biomolecular Chemistry 19, no. 30 (2021): 6697–706. http://dx.doi.org/10.1039/d1ob00742d.
Повний текст джерелаGunaratne, H. Q. Nimal, Tiina Laaksonen, Kenneth R. Seddon, and Kristiina Wähälä. "1-(+)-Dehydroabietylimidazolium Salts as Enantiomer Discriminators for NMR Spectroscopy." Australian Journal of Chemistry 70, no. 7 (2017): 845. http://dx.doi.org/10.1071/ch16545.
Повний текст джерелаLi, Gaowei, Jiangming Cao, Wen Zong, Xinxiang Lei, and Renxiang Tan. "Enantiodiscrimination of carboxylic acids using the diphenylprolinol NMR chiral solvating agents." Organic Chemistry Frontiers 3, no. 1 (2016): 96–102. http://dx.doi.org/10.1039/c5qo00264h.
Повний текст джерелаMoon, Lomary S., Mohan Pal, Yoganjaneyulu Kasetti, Prasad V. Bharatam, and Ravinder S. Jolly. "Chiral Solvating Agents for Cyanohydrins and Carboxylic Acids†." Journal of Organic Chemistry 75, no. 16 (August 20, 2010): 5487–98. http://dx.doi.org/10.1021/jo100445d.
Повний текст джерелаUccello-Barretta, Gloria, Federica Balzano, Jonathan Martinelli, Margherita-Giulia Berni, Claudio Villani, and Francesco Gasparrini. "NMR enantiodiscrimination by cyclic tetraamidic chiral solvating agents." Tetrahedron: Asymmetry 16, no. 22 (November 2005): 3746–51. http://dx.doi.org/10.1016/j.tetasy.2005.10.016.
Повний текст джерелаGIORDANO, C., and A. RESTELLI. "ChemInform Abstract: New Chiral Solvating Agents: 1,5-Benzothiazepines." ChemInform 22, no. 47 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199147290.
Повний текст джерелаLv, Caixia, Lei Feng, Hongmei Zhao, Guo Wang, Pericles Stavropoulos та Lin Ai. "Chiral discrimination of α-hydroxy acids and N-Ts-α-amino acids induced by tetraaza macrocyclic chiral solvating agents by using 1H NMR spectroscopy". Organic & Biomolecular Chemistry 15, № 7 (2017): 1642–50. http://dx.doi.org/10.1039/c6ob02578a.
Повний текст джерелаTayama, Eiji, and Takeshi Sugawara. "Chiral Tetraaryl- and Tetraalkynylborates as Chiral Solvating Agents for Tetraalkylammonium Salts." European Journal of Organic Chemistry 2019, no. 4 (January 11, 2019): 803–11. http://dx.doi.org/10.1002/ejoc.201801448.
Повний текст джерелаChaudhary, Pooja, Geeta Devi Yadav, and Surendra Singh. "A simple protocol for determination of enantiopurity of amines using BINOL derivatives as chiral solvating agents via1H- and 19F-NMR spectroscopic analysis." RSC Advances 12, no. 39 (2022): 25457–64. http://dx.doi.org/10.1039/d2ra05291a.
Повний текст джерелаLiu, Luzhi, Cuiguang Ma, Qin He, Yan Huang, and Wengui Duan. "Effective enantiomeric identification of aromatic amines by tyrosine-modified pillar[5]arenes as chiral NMR solvating agents." Organic Chemistry Frontiers 8, no. 15 (2021): 4144–52. http://dx.doi.org/10.1039/d1qo00525a.
Повний текст джерелаMerelli, Bérangère, Laurence Menguy, Estelle Soubeyrand-Lenoir, and Jean-Claude Cherton. "Determination of the enantiomeric composition of chiral delta-2-thiazolines-1,3 by1H and19F NMR spectroscopy using chiral solvating agents." Spectroscopy 20, no. 3 (2006): 95–107. http://dx.doi.org/10.1155/2006/698685.
Повний текст джерелаYuan, Quan, Enqin Fu, Xiaojun Wu, Maohai Fang, Peng Xue, Chengtai Wu, and Jiahua Chen. "A convenient synthesis of chiral dioxocyclens and application as chiral solvating agents." Tetrahedron Letters 43, no. 21 (May 2002): 3935–37. http://dx.doi.org/10.1016/s0040-4039(02)00623-8.
Повний текст джерелаPeriasamy, Mariappan, Manasi Dalai, and Meduri Padmaja. "Chiral trans-1,2-diaminocyclohexane derivatives as chiral solvating agents for carboxylic acids." Journal of Chemical Sciences 122, no. 4 (July 2010): 561–69. http://dx.doi.org/10.1007/s12039-010-0090-z.
Повний текст джерелаLaaksonen, Tiina, Sami Heikkinen, and Kristiina Wähälä. "Synthesis and applications of secondary amine derivatives of (+)-dehydroabietylamine in chiral molecular recognition." Organic & Biomolecular Chemistry 13, no. 42 (2015): 10548–55. http://dx.doi.org/10.1039/c5ob01667c.
Повний текст джерелаLabuta, Jan, Shinsuke Ishihara, Daniel T. Payne, Kazuyoshi Takimoto, Hisako Sato, Lenka Hanyková, Katsuhiko Ariga, and Jonathan P. Hill. "Estimation of Enantiomeric Excess Based on Rapid Host–Guest Exchange." Chemosensors 9, no. 9 (September 9, 2021): 259. http://dx.doi.org/10.3390/chemosensors9090259.
Повний текст джерелаLuu, Quang H., Kyle G. Lewis, Anik Banerjee, Nattamai Bhuvanesh, and John A. Gladysz. "The robust, readily available cobalt(iii) trication [Co(NH2CHPhCHPhNH2)3]3+ is a progenitor of broadly applicable chirality and prochirality sensing agents." Chemical Science 9, no. 22 (2018): 5087–99. http://dx.doi.org/10.1039/c8sc01510d.
Повний текст джерелаBozkurt, Selahattin. "Calixarene based chiral solvating agents for α-hydroxy carboxylic acids". Journal of Molecular Structure 1048 (вересень 2013): 113–20. http://dx.doi.org/10.1016/j.molstruc.2013.05.032.
Повний текст джерелаWenzel, Thomas J. "Calixarenes and calix[4]resorcinarenes as chiral NMR solvating agents." Journal of Inclusion Phenomena and Macrocyclic Chemistry 78, no. 1-4 (April 30, 2013): 1–14. http://dx.doi.org/10.1007/s10847-013-0325-y.
Повний текст джерелаRudzińska-Szostak, Ewa, Łukasz Górecki, Łukasz Berlicki, Katarzyna Ślepokura, and Artur Mucha. "Zwitterionic Phosphorylated Quinines as Chiral Solvating Agents for NMR Spectroscopy." Chirality 27, no. 10 (August 25, 2015): 752–60. http://dx.doi.org/10.1002/chir.22494.
Повний текст джерелаPuentes, Cira Mollings, and Thomas J. Wenzel. "Phosphated cyclodextrins as water-soluble chiral NMR solvating agents for cationic compounds." Beilstein Journal of Organic Chemistry 13 (January 6, 2017): 43–53. http://dx.doi.org/10.3762/bjoc.13.6.
Повний текст джерелаLuo, Zengwei, Baohua Li, Xiantao Fang, Kai Hu, Xiaojun Wu та Enqin Fu. "Novel chiral solvating agents derived from natural amino acid: enantiodiscrimination for chiral α-arylalkylamines". Tetrahedron Letters 48, № 10 (березень 2007): 1753–56. http://dx.doi.org/10.1016/j.tetlet.2007.01.036.
Повний текст джерелаPERIASAMY, MARIAPPAN, MANASI DALAI, and MEDURI PADMAJA. "Erratum to: Chiral trans-1,2-diaminocyclohexane derivatives as chiral solvating agents for carboxylic acids." Journal of Chemical Sciences 123, no. 3 (May 2011): 365. http://dx.doi.org/10.1007/s12039-011-0144-x.
Повний текст джерелаSheshenev, Andrey E., Ekaterina V. Boltukhina, Anastasiya A. Grishina, Ivana Cisařova, Ilya M. Lyapkalo, and King Kuok Mimi Hii. "New Chiral Zwitterionic Phosphorus Heterocycles: Synthesis, Structure, Properties and Application as Chiral Solvating Agents." Chemistry - A European Journal 19, no. 25 (April 18, 2013): 8136–43. http://dx.doi.org/10.1002/chem.201300062.
Повний текст джерелаBłaszczyk, Jarosław, Bogdan Bujnicki, Patrycja Pokora-Sobczak, Grażyna Mielniczak, Lesław Sieroń, Piotr Kiełbasiński, and Józef Drabowicz. "New Optically Active tert-Butylarylthiophosphinic Acids and Their Selenium Analogues as the Potential Synthons of Supramolecular Organometallic Complexes: Syntheses and Crystallographic Structure Determination." Molecules 28, no. 11 (May 24, 2023): 4298. http://dx.doi.org/10.3390/molecules28114298.
Повний текст джерелаQuinn, Thomas P., Philip D. Atwood, Joseph M. Tanski, Tyler F. Moore, and J. Frantz Folmer-Andersen. "Aza-Crown Macrocycles as Chiral Solvating Agents for Mandelic Acid Derivatives." Journal of Organic Chemistry 76, no. 24 (December 16, 2011): 10020–30. http://dx.doi.org/10.1021/jo2018203.
Повний текст джерелаBenedict, Brooke, Christopher E. Lietz, and Thomas J. Wenzel. "Comparison of chiral NMR solvating agents for the enantiodifferentiation of amines." Tetrahedron 74, no. 37 (September 2018): 4846–56. http://dx.doi.org/10.1016/j.tet.2018.07.053.
Повний текст джерелаYang, Lu, Thomas Wenzel, R. Thomas Williamson, Melodie Christensen, Wes Schafer, and Christopher J. Welch. "Expedited Selection of NMR Chiral Solvating Agents for Determination of Enantiopurity." ACS Central Science 2, no. 5 (April 20, 2016): 332–40. http://dx.doi.org/10.1021/acscentsci.6b00062.
Повний текст джерелаLiu, Lu, Mingde Ye, Xingen Hu, Xiaochun Yu, Lixue Zhang, and Xinxiang Lei. "Chiral solvating agents for carboxylic acids based on the salen moiety." Tetrahedron: Asymmetry 22, no. 16-17 (September 2011): 1667–71. http://dx.doi.org/10.1016/j.tetasy.2011.09.022.
Повний текст джерелаZonta, Cristiano, Andrej Kolarovic, Miriam Mba, Marta Pontini, E. Peter KÜndig, and Giulia Licini. "Enantiopure Ti(IV) amino triphenolate complexes as NMR chiral solvating agents." Chirality 23, no. 9 (August 17, 2011): 796–800. http://dx.doi.org/10.1002/chir.20994.
Повний текст джерелаWang, Wenge, Fengnian Ma, Xiumin Shen та Cong Zhang. "New chiral auxiliaries derived from (S)-α-phenylethylamine as chiral solvating agents for carboxylic acids". Tetrahedron: Asymmetry 18, № 7 (квітень 2007): 832–37. http://dx.doi.org/10.1016/j.tetasy.2007.03.030.
Повний текст джерелаWang, Wenge, Xiumin Shen, Fengnian Ma, Zijing Li, and Cong Zhang. "Chiral amino alcohols derived from natural amino acids as chiral solvating agents for carboxylic acids." Tetrahedron: Asymmetry 19, no. 10 (May 2008): 1193–99. http://dx.doi.org/10.1016/j.tetasy.2008.04.030.
Повний текст джерелаFeng, Si, Liangyuan Yao, Fengliang Liu, Xiao Zeng, and Junjie Wang. "Synthesis of noval chiral tridentate amino alcohols as chiral solvating agents under ball-milling conditions." Tetrahedron Letters 59, no. 49 (December 2018): 4305–10. http://dx.doi.org/10.1016/j.tetlet.2018.10.049.
Повний текст джерелаKoy, Cornelia, Manfred Michalik, Christian Döbler, and Günther Oehme. "Chiral Recognition of Aminoalcohols by1H and13C NMR Spectroscopy using binaphthyl derivatives as chiral solvating agents." Journal für Praktische Chemie/Chemiker-Zeitung 339, no. 1 (1997): 660–63. http://dx.doi.org/10.1002/prac.199733901119.
Повний текст джерелаErol Gunal, Sule, Senel Teke Tuncel, and Ilknur Dogan. "Enantiodiscrimination of carboxylic acids using single enantiomer thioureas as chiral solvating agents." Tetrahedron 76, no. 18 (May 2020): 131141. http://dx.doi.org/10.1016/j.tet.2020.131141.
Повний текст джерелаPérez-Trujillo, Míriam, Eva Monteagudo, and Teodor Parella. "13C NMR Spectroscopy for the Differentiation of Enantiomers Using Chiral Solvating Agents." Analytical Chemistry 85, no. 22 (November 6, 2013): 10887–94. http://dx.doi.org/10.1021/ac402580j.
Повний текст джерелаMa, Fengnian, Xiumin Shen, Jie Ou-Yang, Zhiwei Deng, and Cong Zhang. "Macrocyclic compounds as chiral solvating agents for phosphinic, phosphonic, and phosphoric acids." Tetrahedron: Asymmetry 19, no. 1 (January 2008): 31–37. http://dx.doi.org/10.1016/j.tetasy.2007.12.004.
Повний текст джерелаDalvano, Brielle E., and Thomas J. Wenzel. "Sulfated cyclodextrins as water-soluble chiral NMR solvating agents for cationic compounds." Tetrahedron: Asymmetry 28, no. 8 (August 2017): 1061–69. http://dx.doi.org/10.1016/j.tetasy.2017.07.003.
Повний текст джерелаWenzel, Thomas J. "ChemInform Abstract: Calixarenes and Calix[4]resorcinarenes as Chiral NMR Solvating Agents." ChemInform 46, no. 11 (February 24, 2015): no. http://dx.doi.org/10.1002/chin.201511347.
Повний текст джерелаHoffmann, Herbert C., Silvia Paasch, Philipp Müller, Irena Senkovska, Mohan Padmanaban, Frank Glorius, Stefan Kaskel, and Eike Brunner. "Chiral recognition in metal–organic frameworks studied by solid-state NMR spectroscopy using chiral solvating agents." Chemical Communications 48, no. 85 (2012): 10484. http://dx.doi.org/10.1039/c2cc35366k.
Повний текст джерелаYang, Xuemei, Xiaojun Wu, Maohai Fang, Quan Yuan, and Enqin Fu. "Novel rigid chiral macrocyclic dioxopolyamines derived from l-proline as chiral solvating agents for carboxylic acids." Tetrahedron: Asymmetry 15, no. 16 (August 2004): 2491–97. http://dx.doi.org/10.1016/j.tetasy.2004.07.016.
Повний текст джерелаYi, Jingyu, Guoxin Du, Yaxi Yang, Yuanchao Li, Yiming Li, and Fujiang Guo. "Chiral discrimination of natural isoflavanones using (R)- and (S)-BINOL as the NMR chiral solvating agents." Tetrahedron: Asymmetry 27, no. 22-23 (December 2016): 1153–59. http://dx.doi.org/10.1016/j.tetasy.2016.09.002.
Повний текст джерелаTabassum, Sobia, Mazhar Amjad Gilani, and René Wilhelm. "Imidazolinium sulfonate and sulfamate zwitterions as chiral solvating agents for enantiomeric excess calculations." Tetrahedron: Asymmetry 22, no. 16-17 (September 2011): 1632–39. http://dx.doi.org/10.1016/j.tetasy.2011.09.018.
Повний текст джерелаO'Farrell, Courtney M., J. Matthew Chudomel, Jan M. Collins, Catherine F. Dignam, and Thomas J. Wenzel. "Water-Soluble Calix[4]resorcinarenes with Hydroxyproline Groups as Chiral NMR Solvating Agents." Journal of Organic Chemistry 73, no. 7 (April 2008): 2843–51. http://dx.doi.org/10.1021/jo702751z.
Повний текст джерелаWilhelm, René, Mazhar Gilani та Eduard Rais. "Chiral Imidazolinium Salts with TIPS Groups for the Palladium-Catalyzed α-Arylation and as Chiral Solvating Agents". Synlett 26, № 11 (18 червня 2015): 1638–41. http://dx.doi.org/10.1055/s-0034-1381012.
Повний текст джерелаYang, Xuemei, Guitao Wang, Cheng Zhong, Xiaojun Wu, and Enqin Fu. "Novel NMR chiral solvating agents derived from (1R,2R)-diaminocyclohexane: synthesis and enantiodiscrimination for chiral carboxylic acids." Tetrahedron: Asymmetry 17, no. 6 (March 2006): 916–21. http://dx.doi.org/10.1016/j.tetasy.2006.03.011.
Повний текст джерелаAltava, Belén, M. Isabel Burguete, Noèlia Carbó, Jorge Escorihuela та Santiago V. Luis. "Chiral bis(amino amides) as chiral solvating agents for enantiomeric excess determination of α-hydroxy and arylpropionic acids". Tetrahedron: Asymmetry 21, № 8 (квітень 2010): 982–89. http://dx.doi.org/10.1016/j.tetasy.2010.05.010.
Повний текст джерелаO’Farrell, Courtney M., and Thomas J. Wenzel. "Water-soluble calix[4]resorcinarenes as chiral NMR solvating agents for phenyl-containing compounds." Tetrahedron: Asymmetry 19, no. 15 (August 2008): 1790–96. http://dx.doi.org/10.1016/j.tetasy.2008.07.023.
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