Статті в журналах з теми "Imine acids"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Imine acids".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Переглядайте статті в журналах для різних дисциплін та оформлюйте правильно вашу бібліографію.
Zarei, Maaroof. "One-step Synthesis of β-lactams Using Cyanuric Fluoride". Journal of Chemical Research 37, № 1 (січень 2013): 25–27. http://dx.doi.org/10.3184/174751912x13545429290478.
Повний текст джерелаWulff, William, Xin Zhang та Yijing Dai. "The Acceleration of the Rearrangement of α-Hydroxy Aldimines by Lewis or Brønsted Acids". Synlett 29, № 15 (28 серпня 2018): 2015–18. http://dx.doi.org/10.1055/s-0037-1610262.
Повний текст джерелаSikervar, Vikas, Ravindra Sonawane, Raghuramaiah Mandadapu, Amol Satish Dehade, Shrikant Abhiman Shete, and Mark Montgomery. "Lewis Acid Mediated [3+2] and [3+3] Annulations of an Azomethine Imine with Donor–Acceptor Cyclopropanes." Synthesis 53, no. 16 (May 10, 2021): 2865–73. http://dx.doi.org/10.1055/a-1503-8068.
Повний текст джерелаMorales Salazar, Daniel, Arvind Kumar Gupta та Andreas Orthaber. "Reactivity studies of an imine-functionalised phosphaalkene; unusual electrostatic and supramolecular stabilisation of a σ2λ3-phosphorus motif via hydrogen bonding". Dalton Transactions 47, № 31 (2018): 10404–9. http://dx.doi.org/10.1039/c8dt01607k.
Повний текст джерелаAlex, S., P. Turcotte, R. Fournier, and D. Vocelle. "Study of the protonation of simple Schiff bases in solvents of various polarity by means of Raman spectroscopy." Canadian Journal of Chemistry 69, no. 2 (February 1, 1991): 239–45. http://dx.doi.org/10.1139/v91-038.
Повний текст джерелаWang, Hao-Ran, En-He Huang, Chen Luo, Wen-Feng Luo, Yin Xu, Peng-Cheng Qian, Jin-Mei Zhou, and Long-Wu Ye. "Copper-catalyzed tandem cis-carbometallation/cyclization of imine-ynamides with arylboronic acids." Chemical Communications 56, no. 35 (2020): 4832–35. http://dx.doi.org/10.1039/d0cc01424a.
Повний текст джерелаBissonnette, Martine, Hoa Le Thanh, and Daniel Vocelle. "Interaction of strong acids with a conjugated imine." Canadian Journal of Chemistry 63, no. 8 (August 1, 1985): 2298–302. http://dx.doi.org/10.1139/v85-379.
Повний текст джерелаBakulina, Olga, Alexander Ivanov, Vitalii Suslonov, Dmitry Dar’in, and Mikhail Krasavin. "A speedy route to sterically encumbered, benzene-fused derivatives of privileged, naturally occurring hexahydropyrrolo[1,2-b]isoquinoline." Beilstein Journal of Organic Chemistry 13 (July 18, 2017): 1413–24. http://dx.doi.org/10.3762/bjoc.13.138.
Повний текст джерелаZaccheria, Federica, Federica Santoro, Elvina Iftitah, and Nicoletta Ravasio. "Brønsted and Lewis Solid Acid Catalysts in the Valorization of Citronellal." Catalysts 8, no. 10 (September 22, 2018): 410. http://dx.doi.org/10.3390/catal8100410.
Повний текст джерелаAhmad, Rasool, Rizwan, Altaf, Rashid, Mahmood, and Ayub. "Role of Pyridine Nitrogen in Palladium-Catalyzed Imine Hydrolysis: A Case Study of (E)-1-(3-bromothiophen-2-yl)-N-(4-methylpyridin-2-yl)methanimine." Molecules 24, no. 14 (July 17, 2019): 2609. http://dx.doi.org/10.3390/molecules24142609.
Повний текст джерелаJung, Seunghee, Yuya Kawashima, Takuya Noguchi та Nobuyuki Imai. "Synthesis of Acetaminophen Analogues Containing α-Amino Acids and Fatty Acids for Inhibiting Hepatotoxicity". Synthesis 51, № 19 (15 липня 2019): 3683–96. http://dx.doi.org/10.1055/s-0037-1611893.
Повний текст джерелаSawada, Daichi, Ayana Hirono, Kouichi Asakura, and Taisuke Banno. "pH-Tolerant giant vesicles composed of cationic lipids with imine linkages and oleic acids." RSC Advances 10, no. 56 (2020): 34247–53. http://dx.doi.org/10.1039/d0ra06822e.
Повний текст джерелаWang, Guohong, Min Li, Wenmin Pang, Min Chen, and Chen Tan. "Lewis acids in situ modulate pyridazine-imine Ni catalysed ethylene (co)polymerisation." New Journal of Chemistry 43, no. 34 (2019): 13630–34. http://dx.doi.org/10.1039/c9nj01243e.
Повний текст джерелаList, Benjamin, Vijay N. Wakchaure, and Carla Obradors. "Chiral Brønsted Acids Catalyze Asymmetric Additions to Substrates that Are Already Protonated: Highly Enantioselective Disulfonimide-Catalyzed Hantzsch Ester Reductions of NH–Imine Hydrochloride Salts." Synlett 31, no. 17 (August 14, 2020): 1707–12. http://dx.doi.org/10.1055/s-0040-1706413.
Повний текст джерелаLivingstone, Keith, Sophie Bertrand, Jenna Mowat, and Craig Jamieson. "Metal-free C–C bond formation via coupling of nitrile imines and boronic acids." Chemical Science 10, no. 44 (2019): 10412–16. http://dx.doi.org/10.1039/c9sc03032h.
Повний текст джерелаShatskiy, Andrey, Anton Axelsson, Elena V. Stepanova, Jian-Quan Liu, Azamat Z. Temerdashev, Bhushan P. Kore, Björn Blomkvist, James M. Gardner, Peter Dinér та Markus D. Kärkäs. "Stereoselective synthesis of unnatural α-amino acid derivatives through photoredox catalysis". Chemical Science 12, № 15 (2021): 5430–37. http://dx.doi.org/10.1039/d1sc00658d.
Повний текст джерелаKOBAYASHI, Shû, and Haruro ISHITANI. "Catalytic Activation of Imine Derivatives Using Novel Lewis Acids." Journal of Synthetic Organic Chemistry, Japan 56, no. 5 (1998): 357–67. http://dx.doi.org/10.5059/yukigoseikyokaishi.56.357.
Повний текст джерелаRoche, Stéphane P. "In the Pursuit of (Ald)Imine Surrogates for the Direct Asymmetric Synthesis of Non-Proteinogenic α-Amino Acids". Synthesis 53, № 16 (24 березня 2021): 2767–76. http://dx.doi.org/10.1055/a-1463-4266.
Повний текст джерелаMeyer, Timo, Nadine Zumbrägel, Christina Geerds, Harald Gröger, and Hartmut H. Niemann. "Structural Characterization of an S-enantioselective Imine Reductase from Mycobacterium Smegmatis." Biomolecules 10, no. 8 (July 31, 2020): 1130. http://dx.doi.org/10.3390/biom10081130.
Повний текст джерелаHartshorn, RM, та AM Sargeson. "Reactions of Chelated β-Functionalized Amino Acids With Thionyl Chloride". Australian Journal of Chemistry 45, № 1 (1992): 5. http://dx.doi.org/10.1071/ch9920005.
Повний текст джерелаCanta, Alessandra, Karin I. Öberg, and Mahesh Rajappan. "The Formation of Imines and Nitriles during VUV Photoirradiation of NH3:C2H x Ice Mixtures." Astrophysical Journal 953, no. 1 (August 1, 2023): 81. http://dx.doi.org/10.3847/1538-4357/acda99.
Повний текст джерелаLu, S. P., та Anita H. Lewin. "Enamine/imine tautomerism in α,β-unsaturated-α-amino acids". Tetrahedron 54, № 50 (грудень 1998): 15097–104. http://dx.doi.org/10.1016/s0040-4020(98)00908-9.
Повний текст джерелаZagraniarsky, Yulian, Bojidarka Ivanova, Karamfil Nikolov, Sabi Varbanov та Tsvetanka Cholakova. "Synthesis of Dimethylphosphinyl-substituted α-Amino(aryl)methylphosphonic Acids and Their Esters". Zeitschrift für Naturforschung B 63, № 10 (1 жовтня 2008): 1192–98. http://dx.doi.org/10.1515/znb-2008-1009.
Повний текст джерелаWang, Ziyang, Xiao Lin, Xuling Chen, Pengfei Li, and Wenjun Li. "Organocatalytic stereoselective 1,6-addition of thiolacetic acids to alkynyl indole imine methides: access to axially chiral sulfur-containing tetrasubstituted allenes." Organic Chemistry Frontiers 8, no. 13 (2021): 3469–74. http://dx.doi.org/10.1039/d1qo00394a.
Повний текст джерелаMonnier, Karin, Gérard Schmitt, Bernard Laude, Marie-France Mercier, Marek M. Kubicki, and Michel Jannin. "Étude de la stéréochimie de la réaction de cycloaddition dipolaire-1,3 de quelques 5-phényl-3,6-dihydro-2H-1,4-oxazin-2-ones avec les N-méthyl et N-phénylmaléimides." Canadian Journal of Chemistry 73, no. 2 (February 1, 1995): 181–90. http://dx.doi.org/10.1139/v95-027.
Повний текст джерелаHussein, Buthaina, Laurance M. S. Bourghli, Muhammed Alzweiri, Yusuf Al-Hiari, Mohammad Abu Sini, Soraya Alnabulsi, and Batool Al-Ghwairi. "Synthesis and Biological Evaluation of Carbonic Anhydrase III and IX Inhibitors using Gas Chromatography with Modified pH Sensitive Pellets." Jordan Journal of Pharmaceutical Sciences 16, no. 2 (July 24, 2023): 426–39. http://dx.doi.org/10.35516/jjps.v16i2.1470.
Повний текст джерелаHammershoei, Anders, Richard M. Hartshorn, and Alan M. Sargeson. "Oxidation of chelated amino acids to imine derivatives with thionyl chloride." Inorganic Chemistry 29, no. 22 (October 1990): 4525–30. http://dx.doi.org/10.1021/ic00347a039.
Повний текст джерелаKOBAYASHI, S., and H. ISHITANI. "ChemInform Abstract: Catalytic Activation of Imine Derivatives Using Novel Lewis Acids." ChemInform 29, no. 42 (June 19, 2010): no. http://dx.doi.org/10.1002/chin.199842298.
Повний текст джерелаTrifonov, Latchezar S., and Alexander S. Orahovats. "Cycloaddition of Carbodiimides and Triphenylketen-imine to Allenic Acids. Preliminary Communication." Helvetica Chimica Acta 69, no. 7 (October 29, 1986): 1585–87. http://dx.doi.org/10.1002/hlca.19860690711.
Повний текст джерелаZahardis, J., S. Geddes, and G. A. Petrucci. "The ozonolysis of primary aliphatic amines in single and multicomponent fine particles." Atmospheric Chemistry and Physics Discussions 7, no. 5 (October 15, 2007): 14603–38. http://dx.doi.org/10.5194/acpd-7-14603-2007.
Повний текст джерелаZahardis, J., S. Geddes, and G. A. Petrucci. "The ozonolysis of primary aliphatic amines in fine particles." Atmospheric Chemistry and Physics 8, no. 5 (February 29, 2008): 1181–94. http://dx.doi.org/10.5194/acp-8-1181-2008.
Повний текст джерелаBacha, Katia, Julien Estager, Sylvie Brassart-Pasco, Catherine Chemotti, Antony E. Fernandes, Jean-Pierre Mbakidi, Magali Deleu, and Sandrine Bouquillon. "Synthesis and Activity of Ionic Antioxidant-Functionalized PAMAMs and PPIs Dendrimers." Polymers 14, no. 17 (August 27, 2022): 3513. http://dx.doi.org/10.3390/polym14173513.
Повний текст джерелаWu, Anxin, Jungang Wang, Yan Cheng та Jiachen Xiang. "Synthesis of 2,5-Disubstituted Oxazoles from Arylacetylenes and α-Amino Acids through an I2/Cu(NO3)2•3H2O-Assisted Domino Sequence". Synlett 30, № 06 (7 лютого 2019): 743–47. http://dx.doi.org/10.1055/s-0037-1612087.
Повний текст джерелаCarvalho, M. Fernanda N. N., M. João Ferreira, Ana S. O. Knittel, Maria da Conceição Oliveira, João Costa Pessoa, Rudolf Herrmann, and Gabriele Wagner. "Strecker degradation of amino acids promoted by a camphor-derived sulfonamide." Beilstein Journal of Organic Chemistry 12 (April 18, 2016): 732–44. http://dx.doi.org/10.3762/bjoc.12.73.
Повний текст джерелаSenthil Kumar Raju, Archana Settu, Archana Thiyagarajan, Divya Rama, Praveen Sekar, and Shridharshini Kumar. "Synthetic approaches of medicinally important Schiff bases: An updated Review." World Journal of Advanced Research and Reviews 16, no. 3 (December 30, 2022): 838–52. http://dx.doi.org/10.30574/wjarr.2022.16.3.1394.
Повний текст джерелаShavrina, Oksana, Lyudmyla Bezgubenko, Andrii Bezdudny, Petro Onys’ko та Yuliya Rassukana. "α-(Imino)pyridyldifluoroethyl Phosphonates: Novel Promising Building Blocks in Synthesis of Biorelevant Aminophosphonic Acids Derivatives". Organics 2, № 2 (23 квітня 2021): 72–83. http://dx.doi.org/10.3390/org2020007.
Повний текст джерелаRössner, J., J. Velíšek, F. Pudil, and J. Davídek. "Strecker degradation products of aspartic and glutamic acids and their amides." Czech Journal of Food Sciences 19, No. 2 (February 7, 2013): 41–45. http://dx.doi.org/10.17221/6573-cjfs.
Повний текст джерелаTruong, Vouy Linh, and Jennifer Y. Pfeiffer. "Rhodium-catalyzed diastereoselective 1,2-addition of arylboronic acids to chiral trifluoroethyl imine." Tetrahedron Letters 50, no. 14 (April 2009): 1633–35. http://dx.doi.org/10.1016/j.tetlet.2009.01.112.
Повний текст джерелаRoy, Susmita, Tanmay Chatterjee, Biplab Banerjee, Noor Salam, Asim Bhaumik, and Sk Manirul Islam. "Cu(ii) anchored nitrogen-rich covalent imine network (CuII-CIN-1): an efficient and recyclable heterogeneous catalyst for the synthesis of organoselenides from aryl boronic acids in a green solvent." RSC Adv. 4, no. 86 (2014): 46075–83. http://dx.doi.org/10.1039/c4ra08909j.
Повний текст джерелаMcGregor, Nicholas, Christophe Pardin, and W. G. Skene. "Using Quenching Kinetics and Thermodynamics of Amino-Fluorophores as Empirical Tools for Predicting Boronic Acid Sensors Suitable for Use in Physiological Conditions." Australian Journal of Chemistry 64, no. 11 (2011): 1438. http://dx.doi.org/10.1071/ch11297.
Повний текст джерелаDurai, Chandramathi R. Sherman, and Margaret M. Harding. "Targeting Nucleic Acids using Dynamic Combinatorial Chemistry." Australian Journal of Chemistry 64, no. 6 (2011): 671. http://dx.doi.org/10.1071/ch11023.
Повний текст джерелаFilatov, Vadim E., Dmitrii A. Iuzabchuk, Viktor A. Tafeenko, Yuri K. Grishin, Vitaly A. Roznyatovsky, Dmitrii A. Lukianov, Yulia A. Fedotova та ін. "Dispirooxindole-β-Lactams: Synthesis via Staudinger Ketene-Imine Cycloaddition and Biological Evaluation". International Journal of Molecular Sciences 23, № 12 (15 червня 2022): 6666. http://dx.doi.org/10.3390/ijms23126666.
Повний текст джерелаFulton, Ronnie L., and Diana M. Downs. "DadY (PA5303) is required for fitness of Pseudomonas aeruginosa when growth is dependent on alanine catabolism." microbial Cell 9, no. 12 (December 5, 2022): 190–201. http://dx.doi.org/10.15698/mic2022.12.788.
Повний текст джерелаYao, Suyang, Yanxi Pu, Lulu Ren, Manli Cao та Baohui Ye. "Photooxidative Dehydrogenation of Chiral Ir (III) Amino Acid Complexes Based on [Λ-Ir(ppy)2(MeCN)2](PF6)". Inorganics 11, № 10 (25 вересня 2023): 380. http://dx.doi.org/10.3390/inorganics11100380.
Повний текст джерелаHAMMERSHOEI, A., R. M. HARTSHORN, and A. M. SARGESON. "ChemInform Abstract: Oxidation of Chelated Amino Acids to Imine Derivatives with Thionyl Chloride." ChemInform 22, no. 8 (August 23, 2010): no. http://dx.doi.org/10.1002/chin.199108117.
Повний текст джерелаCossette, Daniel, and Daniel Vocelle. "A 13C and 15N nuclear magnetic resonance study of the protonation of a retinal Schiff base by acids of different pKas and in solvents of different polarities." Canadian Journal of Chemistry 65, no. 7 (July 1, 1987): 1576–83. http://dx.doi.org/10.1139/v87-265.
Повний текст джерелаMondal, Sanjoy, Partha Bairi, Sujoy Das, and Arun K. Nandi. "Phase selective organogel from an imine based gelator for use in oil spill recovery." Journal of Materials Chemistry A 7, no. 1 (2019): 381–92. http://dx.doi.org/10.1039/c8ta09732a.
Повний текст джерелаBissonnette, Martine, Hoa Le Thanh, and Daniel Vocelle. "Étude d'un modèle simplifié de la rhodopsine: la toute trans-rétinylidène tert-butylamine en présence de divers acides carboxyliques." Canadian Journal of Chemistry 63, no. 7 (July 1, 1985): 1480–86. http://dx.doi.org/10.1139/v85-254.
Повний текст джерелаFisyuk, Alexander, Ivan Kulakov, Anton Shatsauskas, Mariya Matsukevich, Irina Palamarchuk, Tulegen Seilkhanov, and Yuriy Gatilov. "A New Approach to the Synthesis of Benzo[c][1,7]naphthyridin-4(3H)-ones." Synthesis 49, no. 16 (June 7, 2017): 3700–3709. http://dx.doi.org/10.1055/s-0036-1590470.
Повний текст джерелаMikami, Koichi, Masami Kaneko та Tomoko Yajima. "Asymmetric imine-ene reactions with chiral glyoxylate-derived α-imino esters: An efficient route to asymmetric synthesis of α-amino acids". Tetrahedron Letters 34, № 30 (липень 1993): 4841–42. http://dx.doi.org/10.1016/s0040-4039(00)74104-9.
Повний текст джерела