Статті в журналах з теми "Ketenimine"
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Baradarani, M., RH Prager, and K. Schafer. "The Chemistry of 5-Oxodihydroisoxazoles. XV. Reaction of Derived Ketenimines With Enamines and Enolates." Australian Journal of Chemistry 49, no. 8 (1996): 911. http://dx.doi.org/10.1071/ch9960911.
Повний текст джерелаAng, KH, RH Prager, and CM Williams. "The Chemistry of 5-Oxodihydroisoxazoles. XII. Trapping of Derived Ketenimines With Lithium Amides and Alkyllithiums." Australian Journal of Chemistry 48, no. 1 (1995): 55. http://dx.doi.org/10.1071/ch9950055.
Повний текст джерелаYavari, Issa, Farough Nasiri, Hoorieh Djahaniani, and Hamid R. Bijanzadeh. "Synthesis and Dynamic NMR Study of Fluorinated Dialkyl 2-[(tert-butylimino)-methylene]-3-[(2-alkoxy-2-oxoacetyl)-2-fluoroanilino]-succinates." Journal of Chemical Research 2005, no. 8 (August 2005): 537–39. http://dx.doi.org/10.3184/030823405774663372.
Повний текст джерелаAlajarín, Mateo, Baltasar Bonillo, Pilar Sánchez-Andrada, Ángel Vidal, and Delia Bautista. "Intramolecular Ketenimine−Ketenimine [2 + 2] and [4 + 2] Cycloadditions†." Journal of Organic Chemistry 72, no. 15 (July 2007): 5863–66. http://dx.doi.org/10.1021/jo0704661.
Повний текст джерелаHe, Wenxing, Xiaojun Tan, Nana Wang, and Hong Zhang. "Theoretical study on the mechanism of the cycloaddition reaction between ketenimine and hydrogen cyanide." Journal of the Serbian Chemical Society 81, no. 2 (2016): 187–95. http://dx.doi.org/10.2298/jsc150504091h.
Повний текст джерелаBrown, RFC, KJ Coulston, and FW Eastwood. "Intramolecular Trapping of a Ketenimine Carbene Formed on Flash Vacuum Pyrolysis of 3-Phenylimino-3H-indazole and 3-Phenyliminoisobenzofuran-1-one." Australian Journal of Chemistry 47, no. 1 (1994): 47. http://dx.doi.org/10.1071/ch9940047.
Повний текст джерелаSaraví Cisneros, Hebe, Sergio Laurella, Danila L. Ruiz, Agustín Ponzinibbio, Patricia E. Allegretti, and Jorge J. P. Furlong. "Spectrometric Study of the Nitrile-Ketenimine Tautomerism." International Journal of Spectroscopy 2009 (September 9, 2009): 1–18. http://dx.doi.org/10.1155/2009/408345.
Повний текст джерелаCapuano, Lilly, and Keramatollah Djokar. "N-Funktionalisierte Ketenimine, II." Liebigs Annalen der Chemie 1985, no. 12 (December 22, 1985): 2305–12. http://dx.doi.org/10.1002/jlac.198519851202.
Повний текст джерелаCen, Mengjie, Qiaoyi Xiang, Yiwen Xu, Shengguo Duan, Yaohong Lv, Ze-Feng Xu та Chuan-Ying Li. "Synthesis of α-cyano sulfone via thermal rearrangement of 1,4-disubstituted triazole mediated by carbene and radical species". Organic Chemistry Frontiers 7, № 3 (2020): 596–601. http://dx.doi.org/10.1039/c9qo01340g.
Повний текст джерелаChauhan, Dinesh Pratapsinh, Sreejith J. Varma, Mahesh Gudem, Nihar Panigrahi, Khushboo Singh, Anirban Hazra, and Pinaki Talukdar. "Intramolecular cascade rearrangements of enynamine derived ketenimines: access to acyclic and cyclic amidines." Organic & Biomolecular Chemistry 15, no. 22 (2017): 4822–30. http://dx.doi.org/10.1039/c7ob00499k.
Повний текст джерелаWolf, Reinhard, Ming Wah Wong, Colin H. L. Kennard, and Curt Wentrup. "A Remarkably Stable Linear Ketenimine." Journal of the American Chemical Society 117, no. 25 (June 1995): 6789–90. http://dx.doi.org/10.1021/ja00130a023.
Повний текст джерелаAlajarin, Mateo, Marta Marin-Luna, and Angel Vidal. "Recent Highlights in Ketenimine Chemistry." European Journal of Organic Chemistry 2012, no. 29 (June 6, 2012): 5637–53. http://dx.doi.org/10.1002/ejoc.201200383.
Повний текст джерелаXu, Ze-Feng, Xing Yu, Dongdong Yang, and Chuan-Ying Li. "Metal-free synthesis of 2-aminonaphthalenes by intramolecular transannulation of 1-sulfonyl-4-(2-alkenylphenyl)-1,2,3-triazoles." Organic & Biomolecular Chemistry 15, no. 15 (2017): 3161–64. http://dx.doi.org/10.1039/c7ob00637c.
Повний текст джерелаAlajarin, Mateo, Baltasar Bonillo, Maria-Mar Ortin, and Angel Vidal. "Ketenimine for Nitrile Rearrangements in N-Arylmethyl Ketenimines: [1,n] Migrations of Bulky Arylmethyl Groups." Letters in Organic Chemistry 7, no. 7 (October 1, 2010): 528–32. http://dx.doi.org/10.2174/157017810793362280.
Повний текст джерелаLi, Guofeng, Man Zhao, Junqiu Xie, Ying Yao, Lingyun Mou, Xiaowei Zhang, Xiaomin Guo та ін. "Efficient synthesis of cyclic amidine-based fluorophores via 6π-electrocyclic ring closure". Chemical Science 11, № 14 (2020): 3586–91. http://dx.doi.org/10.1039/d0sc00798f.
Повний текст джерелаSun, Jiarui, Xiangsheng Cheng, John Kamanda Mansaray, Weihong Fei, Jieping Wan та Weijun Yao. "A copper-catalyzed three component reaction of aryl acetylene, sulfonyl azide and enaminone to form iminolactone via 6π electrocyclization". Chemical Communications 54, № 99 (2018): 13953–56. http://dx.doi.org/10.1039/c8cc06868b.
Повний текст джерелаWang, Baolin, Kota Koshino, and Rei Kinjo. "Bicyclic (amino)(borata)carbene derived from diazadiborinine and isonitrile." Chemical Communications 55, no. 86 (2019): 13012–14. http://dx.doi.org/10.1039/c9cc06453b.
Повний текст джерелаHonrado, Manuel, Sonia Sobrino, Juan Fernández-Baeza, Luis F. Sánchez-Barba, Andrés Garcés, Agustín Lara-Sánchez, and Ana M. Rodríguez. "Synthesis of an enantiopure scorpionate ligand by a nucleophilic addition to a ketenimine and a zinc initiator for the isoselective ROP of rac-lactide." Chemical Communications 55, no. 61 (2019): 8947–50. http://dx.doi.org/10.1039/c9cc04716f.
Повний текст джерелаBalueva, A. S., E. R. Mustakimov, G. N. Nikonov, Yu T. Struchkov, A. P. Pisarevsky, and R. R. Musin. "Interaction ofZ-1,2-borylphosphinoalkene with ketenimine." Russian Chemical Bulletin 45, no. 1 (January 1996): 174–79. http://dx.doi.org/10.1007/bf01433757.
Повний текст джерелаFandos, Rosa, Maurizio Lanfranchi, Antonio Otero, María Angela Pellinghelli, M. José Ruiz, and Jan H. Teuben. "Early-Transition-Metal Ketenimine Complexes: Synthesis, Reactivity, and Structure of Ketenimine-Containing Titanocene and Zirconocene Complexes." Organometallics 16, no. 24 (November 1997): 5283–88. http://dx.doi.org/10.1021/om970568p.
Повний текст джерелаPhilippova, Anna N., Daria V. Vorobyeva, Pavel S. Gribanov, Fedor M. Dolgushin, and Sergey N. Osipov. "Diastereoselective Synthesis of Highly Functionalized Proline Derivatives." Molecules 27, no. 20 (October 14, 2022): 6898. http://dx.doi.org/10.3390/molecules27206898.
Повний текст джерелаKHLEBNIKOV, A. F., M. S. NOVIKOV, and R. R. KOSTIKOV. "ChemInform Abstract: Ketenimine Ylides in the Reactions of Fluorochloro- and Dibromocarbenes with Ketenimines. Synthesis of Carbamoyl Fluorides." ChemInform 22, no. 9 (August 23, 2010): no. http://dx.doi.org/10.1002/chin.199109152.
Повний текст джерелаAlajarin, Mateo, Baltasar Bonillo, Maria-Mar Ortin, and Angel Vidal. "ChemInform Abstract: Ketenimine for Nitrile Rearrangement in N-Arylmethyl Ketenimines: [1,n] Migrations of Bulky Arylmethyl Groups." ChemInform 42, no. 14 (March 14, 2011): no. http://dx.doi.org/10.1002/chin.201114034.
Повний текст джерелаReva, Igor, Hanna Rostkowska, and Leszek Lapinski. "Phototransformations of 2,3-Diamino-2-Butenedinitrile (DAMN) Monomers Isolated in Low-Temperature Argon Matrix." Photochem 2, no. 2 (June 16, 2022): 448–62. http://dx.doi.org/10.3390/photochem2020031.
Повний текст джерелаWOLF, R., M. W. WONG, C. H. L. KENNARD, and C. WENTRUP. "ChemInform Abstract: A Remarkably Stable Linear Ketenimine." ChemInform 26, no. 43 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199543159.
Повний текст джерелаStrecker, Beate, and Helmut Werner. "Ketenimine Complexes from Metal Isocyanides and Diazoalkanes." Angewandte Chemie International Edition in English 29, no. 3 (March 1990): 275–76. http://dx.doi.org/10.1002/anie.199002751.
Повний текст джерелаAlajarin, Mateo, Marta Marin-Luna, and Angel Vidal. "ChemInform Abstract: Recent Highlights in Ketenimine Chemistry." ChemInform 44, no. 13 (March 18, 2013): no. http://dx.doi.org/10.1002/chin.201313208.
Повний текст джерелаGuan, Zhi-Rong, Shuai Liu, Zi-Ming Liu, and Ming-Wu Ding. "One-Pot Three-Component Synthesis of Pyrrolidin-2-ones via a Sequential Wittig/Nucleophilic Addition/Cyclization Reaction." Synthesis 51, no. 11 (March 4, 2019): 2402–8. http://dx.doi.org/10.1055/s-0037-1612279.
Повний текст джерелаKumar, Gadi Ranjith, Yalla Kiran Kumar, Ruchir Kant, and Maddi Sridhar Reddy. "Tandem Cu-catalyzed ketenimine formation and intramolecular nucleophile capture: Synthesis of 1,2-dihydro-2-iminoquinolines from 1-(o-acetamidophenyl)propargyl alcohols." Beilstein Journal of Organic Chemistry 10 (May 28, 2014): 1255–60. http://dx.doi.org/10.3762/bjoc.10.125.
Повний текст джерелаAndersen, Heidi Gade, David Kvaskoff, and Curt Wentrup. "Bisiminopropadienes R-N=C=C=C=N-R from Pyridopyrimidines." Australian Journal of Chemistry 65, no. 6 (2012): 686. http://dx.doi.org/10.1071/ch12039.
Повний текст джерелаWang, Bingze, and Conghao Deng. "Mechanism of the isomerization of azirinylidene to ketenimine." Chemical Physics Letters 142, no. 1-2 (December 1987): 92–95. http://dx.doi.org/10.1016/0009-2614(87)87256-1.
Повний текст джерелаLiu, Yun-Lin, Guo-Shu Chen, and Xiao-Tong Lin. "3-(2-Isocyanoethyl)indole: A Versatile Reagent for Polycyclic Spiroindoline Synthesis." Synlett 31, no. 11 (March 12, 2020): 1033–39. http://dx.doi.org/10.1055/s-0039-1690853.
Повний текст джерелаWentrup, Curt, Ales Reisinger, and David Kvaskoff. "4-Pyridylnitrene and 2-pyrazinylcarbene." Beilstein Journal of Organic Chemistry 9 (April 17, 2013): 754–60. http://dx.doi.org/10.3762/bjoc.9.85.
Повний текст джерелаHuang, Jie, Feng Li, Lei Cui, Shikuan Su, Xueshun Jia, and Jian Li. "Palladium-catalyzed cascade reactions of enynones and isocyanides: access towards functionalized ketenimine and its application." Chemical Communications 56, no. 33 (2020): 4555–58. http://dx.doi.org/10.1039/c9cc09363j.
Повний текст джерелаDegli Esposti, C., L. Dore, and L. Bizzocchi. "Accurate rest-frequencies of ketenimine (CH2CNH) at submillimetre wavelength." Astronomy & Astrophysics 565 (May 2014): A66. http://dx.doi.org/10.1051/0004-6361/201423589.
Повний текст джерелаLee, Vladimir Ya, Henri Ranaivonjatovo, Jean Escudié, Jacques Satgé, Antoine Dubourg, Jean-Paul Declercq, Mikhail P. Egorov, and Oleg M. Nefedov. "An Eight-Membered CyclicC,N-Bis(germadiyl) Bis(ketenimine)." Organometallics 17, no. 8 (April 1998): 1517–22. http://dx.doi.org/10.1021/om971014p.
Повний текст джерелаRodler, M., R. D. Brown, P. D. Godfrey, and B. Kleibömer. "The rotation-inversion spectrum of ketenimine, H2CCNH." Journal of Molecular Spectroscopy 118, no. 1 (July 1986): 267–76. http://dx.doi.org/10.1016/0022-2852(86)90240-7.
Повний текст джерелаBALUEVA, A. S., E. R. MUSTAKIMOV, G. N. NIKONOV, YU T. STRUCHKOV, A. P. PISAREVSKII, and R. R. MUSIN. "ChemInform Abstract: Reaction of (E)-1,2-Borylphoshinoalkene with Ketenimine." ChemInform 27, no. 26 (August 5, 2010): no. http://dx.doi.org/10.1002/chin.199626217.
Повний текст джерелаKvaskoff, David, Ullrich Mitschke, Chris Addicott, Justin Finnerty, Pawel Bednarek, and Curt Wentrup. "Interconversion of Nitrenes, Carbenes, and Nitrile Ylides by Ring Expansion, Ring Opening, Ring Contraction, and Ring Closure: 3-Quinolylnitrene, 2-Quinoxalylcarbene, and 3-Quinolylcarbene." Australian Journal of Chemistry 62, no. 3 (2009): 275. http://dx.doi.org/10.1071/ch08523.
Повний текст джерелаEscandón-Mancilla, Flor María, Alberto Cedillo-Cruz, Raúl Eduardo Gordillo-Cruz, Diego Martínez-Otero, M. V. Basavanag Unnamatla, and Erick Cuevas-Yañez. "N-(p-Toluenesulfonyl)-1-(4′-acetylphenoxy)acrylimidate: Synthesis, Crystal Structure and Theoretical Studies." Molbank 2022, no. 4 (November 28, 2022): M1509. http://dx.doi.org/10.3390/m1509.
Повний текст джерела刘, 燕萍. "Recent Progress of [3,3]-Rearrangement Reaction of Allyl Ketenimine Structure." Journal of Organic Chemistry Research 09, no. 04 (2021): 50–58. http://dx.doi.org/10.12677/jocr.2021.94007.
Повний текст джерелаOsman, O. I. "Theoretical and Computational Study of Tautomerization of Ketenimine to Acetonitrile." Asian Journal of Chemistry 27, no. 8 (2015): 3091–96. http://dx.doi.org/10.14233/ajchem.2015.18907.
Повний текст джерелаRuiz, Javier, Marta P. Gonzalo, Marilín Vivanco, M. Rosario Díaz, and Santiago García-Granda. "A three-component reaction involving isocyanide, phosphine and ketenimine functionalities." Chemical Communications 47, no. 14 (2011): 4270. http://dx.doi.org/10.1039/c0cc05025c.
Повний текст джерелаRahim, Marufur, Nicholas J. Taylor, Shixuan Xin, and Scott Collins. "Synthesis and Structure of Acyclic Bis(ketenimine) Complexes of Zirconium." Organometallics 17, no. 7 (March 1998): 1315–23. http://dx.doi.org/10.1021/om970862h.
Повний текст джерелаYavari, Issa, and Daryoush Tahmassebi. "Configurational Properties of Eight-membered Rings Containing Two Ketenimine Units." Journal of Chemical Research, no. 12 (1998): 782–83. http://dx.doi.org/10.1039/a804014a.
Повний текст джерелаShustov, G. V., A. V. Kachanov, and R. G. Kostyanovskii. "Ketenimine-nitrile rearrangements of N-alkoxyketenimines under their generation conditions." Bulletin of the Russian Academy of Sciences Division of Chemical Science 41, no. 11 (November 1992): 2039–45. http://dx.doi.org/10.1007/bf00863370.
Повний текст джерелаZhao, Hongyang, Yanpeng Xing, Ping Lu, and Yanguang Wang. "Synthesis of 2,3-Disubstituted Quinolines via Ketenimine or Carbodiimide Intermediates." Chemistry - A European Journal 22, no. 42 (September 5, 2016): 15144–50. http://dx.doi.org/10.1002/chem.201603074.
Повний текст джерелаBESTMANN, H. J., and H. LEHNEN. "ChemInform Abstract: Synthesis and Reactions of N-Phenylbis(diethylphosphonato)ketenimine." ChemInform 23, no. 20 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199220248.
Повний текст джерелаWeragoda, Geethika K., Anushree Das, Sujan K. Sarkar, H. Dushanee M. Sriyarathne, Xiaoming Zhang, Bruce S. Ault, and Anna D. Gudmundsdottir. "Singlet Photoreactivity of 3-Methyl-2-phenyl-2H-azirine." Australian Journal of Chemistry 70, no. 4 (2017): 413. http://dx.doi.org/10.1071/ch16604.
Повний текст джерелаHe, Wenxing, Weihua Wang, Xiaojun Tan, and Ping Li. "Theoretical study on the cycloaddition reaction mechanism between ketenimine and acetonitrile." Main Group Chemistry 15, no. 3 (September 15, 2016): 221–30. http://dx.doi.org/10.3233/mgc-160201.
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