Academic literature on the topic 'Azomethine imine'
Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles
Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Azomethine imine.'
Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.
You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.
Journal articles on the topic "Azomethine imine"
Svete, Jurij, Uroš Grošelj, Franc Požgan, and Bogdan Štefane. "Copper-Catalyzed Azomethine Imine–Alkyne Cycloadditions (CuAIAC)." Synthesis 50, no. 23 (October 5, 2018): 4501–24. http://dx.doi.org/10.1055/s-0037-1610284.
Full textSikervar, 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.
Full textKashinath, Dhurke, Kota Sathish, and Sakkani Nagaraju. "Synthesis of Spiro Pyrazolone-Oxindole and Bicyclic Pyrazolone Derivatives via Solvent-Dependent Regioselective Aza-1,4/1,6-Michael and Intramolecular Cycloaddition under Catalyst-Free Conditions." SynOpen 05, no. 02 (April 13, 2021): 123–33. http://dx.doi.org/10.1055/a-1480-9837.
Full textLi, Yan, and Zhiqiang Zhang. "Mechanisms of phosphine-catalyzed [3+3] cycloaddition of ynones and azomethine imines: a DFT study." New Journal of Chemistry 43, no. 34 (2019): 13600–13607. http://dx.doi.org/10.1039/c9nj01943j.
Full textZhang, Xueyun, Zisong Qi, Jian Gao, and Xingwei Li. "Rhodium(iii)-catalyzed C–H alkynylation of azomethine ylides under mild conditions." Org. Biomol. Chem. 12, no. 46 (2014): 9329–32. http://dx.doi.org/10.1039/c4ob01596g.
Full textHu, Shihe, Jian Zhang, and Qiaomei Jin. "DMAP-catalyzed alkylation of isatin N,N′-cyclic azomethine imine 1,3-dipoles with Morita–Baylis–Hillman carbonates." New Journal of Chemistry 42, no. 9 (2018): 7025–29. http://dx.doi.org/10.1039/c8nj00234g.
Full textAnsari, Arshad J., Aabid Abdullah Wani, Antim K. Maurya, Sarika Verma, Vijai K. Agnihotri, Ashoke Sharon, Prasad V. Bharatam, and Devesh M. Sawant. "An unprecedented N- to C-sulfonyl migration in the reaction of azomethine amine and allenoates: access to arylsulfonylmethyl substituted pyrazolo[1,5-c]quinazoline and mechanistic studies." Chemical Communications 55, no. 98 (2019): 14825–28. http://dx.doi.org/10.1039/c9cc06751e.
Full textSuga, Hiroyuki, Masahiro Yoshiwara, Takaaki Yamaguchi, Takashi Bando, Mizuki Taguchi, Ayano Inaba, Yuichi Goto, Ayaka Kikuchi, Kennosuke Itoh, and Yasunori Toda. "Enantioselective synthesis of 8-azabicyclo[3.2.1]octanes via asymmetric 1,3-dipolar cycloadditions of cyclic azomethine ylides using a dual catalytic system." Chemical Communications 55, no. 11 (2019): 1552–55. http://dx.doi.org/10.1039/c8cc09224a.
Full textInturi, Surendra Babu, Biswajit Kalita, and A. Jafar Ahamed. "I2-TBHP-catalyzed one-pot highly efficient synthesis of 4,3-fused 1,2,4-triazoles from N-tosylhydrazones and aromatic N-heterocycles via intermolecular formal 1,3-dipolar cycloaddition." Organic & Biomolecular Chemistry 14, no. 47 (2016): 11061–64. http://dx.doi.org/10.1039/c6ob01926a.
Full textLiu, Anan, Dongge Ma, Yuhang Qian, Jundan Li, Shan Zhai, Yi Wang, and Chuncheng Chen. "A powerful azomethine ylide route mediated by TiO2 photocatalysis for the preparation of polysubstituted imidazolidines." Organic & Biomolecular Chemistry 19, no. 10 (2021): 2192–97. http://dx.doi.org/10.1039/d0ob02277b.
Full textDissertations / Theses on the topic "Azomethine imine"
Lavergne, Kaitlyn. "Synthesis of Azomethine Imines via Alkene Aminocarbonylation and their Derivatization into Pyrazolones." Thesis, Université d'Ottawa / University of Ottawa, 2015. http://hdl.handle.net/10393/32516.
Full textHunt, Ashley D. "Intramolecular Cope-type Hydroamination of Alkenes and Alkynes Using Hydrazides." Thèse, Université d'Ottawa / University of Ottawa, 2011. http://hdl.handle.net/10393/19881.
Full textLemire, Philippe. "Hydrolyse d’α-aminoesters et de 1-amino diesters phosphoniques par intramolécularité temporaire organocatalysée & Synthèse de pyrazolones et de triazolium-olates par isomérisation d’azométhine imines N,N’-cycliques." Thesis, Université d'Ottawa / University of Ottawa, 2019. http://hdl.handle.net/10393/38738.
Full textBongers, Amanda L. "Intermolecular [3+2] Cycloadditions of Imino-isocyanates to Access β-Amino Carbonyl Compounds." Thesis, Université d'Ottawa / University of Ottawa, 2017. http://hdl.handle.net/10393/35698.
Full textGarbay, Guillaume. "Nouvelles voies de synthèse sans métaux d'oligomères et de polymères π-conjugués pour l'électronique organique." Thesis, Bordeaux, 2016. http://www.theses.fr/2016BORD0240/document.
Full textIn this work, synthesis and characterizations of new conjugated polymers are described.These polymers, developed for their integration into devices, have been synthesized via transitionmetalfree polymerizations. Carbazole based polyazomethines have been synthesized via polycondensation reactions between di-substituted carbazoles, bearing amino and formyl functionsin positions 3,6 or 2,7. Optical and electronical properties of such polymers have been studieddepending of the linkage position. A comonomer EDOT has then been integrated into the polymer chain, and impact of such insertion has been studied. Squaric and croconic acid base polymers have also been synthesized. By varying polymerization conditions, optoelectronic properties have been tuned, leading to the formation of polymers exhibiting a white emission. These polymers have then been integrated into OLED, as the active layer. Finally, more original polymers have been synthesized, using more original reactions or monomers such as by forming in situ benzobisthiazole. Other polymers integrating more originals monomers, such a tetrazine or divanillin, have been synthesized. Optoelectronic properties of such materials have been studied for the purpose of their integration into devices
Dhakal, Ram Chandra. "New Approaches To Heterocycle Synthesis: A Greener Route To Structurally Complex Protonated Azomethine Imines, And Their Use In 1,3-Dipolar Cycloadditions." ScholarWorks @ UVM, 2017. http://scholarworks.uvm.edu/graddis/777.
Full textBetit, Lyanne. "Derivatization of Azomethine Imines into beta-Aminocarbonyl Motifs." Thesis, Université d'Ottawa / University of Ottawa, 2015. http://hdl.handle.net/10393/32473.
Full textOmote, Masato. "Development of Asymmetric Syntheses Utilizing C, N-Cyclic Azomethine Imines." 京都大学 (Kyoto University), 2011. http://hdl.handle.net/2433/142393.
Full textCayuelas, Rubio Alberto. "Imino esters as precursors of azomethine ylides in 1,3-dipolar cycloaddition and Mannich reactions." Doctoral thesis, Universidad de Alicante, 2016. http://hdl.handle.net/10045/56477.
Full textNugent, Benjamin M. "Regio- and stereoselective additions to azomethines free radical cyclizations and chiral Bronsted acid catalyzed reactions of imines /." [Bloomington, Ind.] : Indiana University, 2006. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&res_dat=xri:pqdiss&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&rft_dat=xri:pqdiss:3206873.
Full textSource: Dissertation Abstracts International, Volume: 67-01, Section: B, page: 0275. Adviser: Jeffrey N. Johnston. "Title from dissertation home page (viewed Feb. 22, 2007)."
Book chapters on the topic "Azomethine imine"
Suga, Hiroyuki, and Kennosuke Itoh. "Recent Advances in Catalytic Asymmetric 1,3-Dipolar Cycloadditions of Azomethine Imines, Nitrile Oxides, Diazoalkanes, and Carbonyl Ylides." In Methods and Applications of Cycloaddition Reactions in Organic Syntheses, 175–204. Hoboken, New Jersey: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118778173.ch07.
Full textSchantl, J. G. "Reaction of Diazocyanides with Diaryldiazomethanes; Azomethine Imine Trimerization." In Heteroatom Analogues of Aldehydes and Ketones, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-027-00668.
Full textSchantl, J. G. "Acyclic Azomethine Imines." In Heteroatom Analogues of Aldehydes and Ketones, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-027-00645.
Full textSchantl, J. G. "Transformation of Oxo Azomethine Imines into Thioxo Azomethine Imines." In Heteroatom Analogues of Aldehydes and Ketones, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-027-00716.
Full textSchantl, J. G. "Nonclassical "Criss-Cross" Reaction: [3 + 2] Cycloaddition of Dialkyl and Diphenyl Azodicarboxylates and Diphenylketenes; [3 + 2] Cycloaddition of Resulting Azomethine Imine." In Heteroatom Analogues of Aldehydes and Ketones, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-027-00683.
Full text"27.19.5 Azomethine Imines (Update 2017)." In Knowledge Updates: 2017/1, edited by Joule, Krause, Oestreich, Rademann, Schaumann, Wirth, Fuerstner, Schaumann, Thomas, and Trost. Stuttgart: Georg Thieme Verlag, 2017. http://dx.doi.org/10.1055/sos-sd-127-00429.
Full text"Product Class 19: Azomethine Imines." In Category 4. Compounds with Two Carbon Heteroatom Bonds, edited by Padwa and Bellus. Stuttgart: Georg Thieme Verlag, 2005. http://dx.doi.org/10.1055/sos-sd-027-00644.
Full textSchantl, J. G. "Nonclassical "Criss-Cross" Reaction: [3 + 2] Cycloaddition of Azoalkenes with Thiocyanic Acid; [1,4]- Shift of Resulting Azomethine Imine or [3 + 2] Cycloaddition with Thiocyanic Acid." In Heteroatom Analogues of Aldehydes and Ketones, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-027-00684.
Full textSchantl, J. G. "Reaction of Hexafluoroacetone Azine with Alkenes or Alkynes To Give an Azomethine Imine (1:1 Cycloadduct) and/or "Criss-Cross" (Heterobicyclic) Product (1:2 Cycloadduct)." In Heteroatom Analogues of Aldehydes and Ketones, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-027-00710.
Full textSchantl, J. G. "Thermally or Acid-Induced Ring Enlargement of an Azomethine Imine with an Exocyclic Terminal Nitrogen into the Isomer with All Three Atoms in the Ring." In Heteroatom Analogues of Aldehydes and Ketones, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-027-00721.
Full text