Artykuły w czasopismach na temat „Hexahydropyrimidines”
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Moser, Shasta, Ryan Church, M. Brad Peori i Keith Vaughan. "Triazene derivatives of (1,x)-diazacycloalkanes. Part IV.1 Synthesis and characterization of 1-[2-aryl-1-diazenyl]-3-(3-[2-aryl-1-diazenyl]hexahydro-1-pyrimidinylmethyl)hexahydropyrimidines and 1-(5,5-dimethyl-3-[2-aryl-1-diazenyl]hexahydro-1-pyrimidinylmethyl)-5,5-dimethyl-3-[2-aryl-1-diazenyl]hexahydropyrimidines from the reaction of diazonium salts with mixtures of formaldehyde and 1,3-diaminopropanes". Canadian Journal of Chemistry 83, nr 8 (1.08.2005): 1071–83. http://dx.doi.org/10.1139/v05-131.
Pełny tekst źródłaBadamshin, A. G., D. R. Latypova i V. A. Dokichev. "Synthesis of Polyfunctionalized Hexahydropyrimidines". Russian Journal of Organic Chemistry 55, nr 2 (luty 2019): 168–73. http://dx.doi.org/10.1134/s1070428019020076.
Pełny tekst źródłaZelenin, Kirill N., Valeriy V. Alekseyev, Ilya V. Ukraintsev i Igor V. Tselinsky. "2-SUBSTITUTED HEXAHYDROPYRIMIDINES AND THEIR TAUTOMERISM". Organic Preparations and Procedures International 30, nr 1 (luty 1998): 53–61. http://dx.doi.org/10.1080/00304949809355259.
Pełny tekst źródłaKatritzky, Alan R., Sandeep K. Singh i Hai-Ying He. "Novel Syntheses of Hexahydropyrimidines and Tetrahydroquinazolines". Journal of Organic Chemistry 67, nr 9 (maj 2002): 3115–17. http://dx.doi.org/10.1021/jo010927x.
Pełny tekst źródłaLuk'yanov, O. A., G. V. Pokhvisneva i T. V. Ternikova. "N,N?-Diacylated imidazolidines and hexahydropyrimidines". Russian Chemical Bulletin 43, nr 8 (sierpień 1994): 1376–80. http://dx.doi.org/10.1007/bf00703698.
Pełny tekst źródłaFarrell, Joshua R., Jonathan Niconchuk, Christine S. Higham i Brittany W. Bergeron. "Phenol derivatized hexahydropyrimidines prepared from Mannich condensations". Tetrahedron Letters 48, nr 45 (listopad 2007): 8034–36. http://dx.doi.org/10.1016/j.tetlet.2007.09.038.
Pełny tekst źródłaShafikova, E. A., D. V. Petrov, T. A. Sapozhnikova, N. J. Baschenko i V. A. Dokichev. "Synthesis of norbornane series tetra- and hexahydropyrimidines". Chemistry of Heterocyclic Compounds 45, nr 6 (czerwiec 2009): 685–90. http://dx.doi.org/10.1007/s10593-009-0328-1.
Pełny tekst źródłaTingley, Reid, M. Brad Peori, Ryan Church i Keith Vaughan. "Triazene derivatives of (1,x)-diazacycloalkanes. Part V.1 Synthesis and characterization of 4-ethyl-3-({6-ethyl-3-[2-aryl-1-diazenyl]hexahydro-1-pyrimidinyl}methyl)-1-[2-aryl-1-diazenyl)hexa- hydropyrimidines from the reaction of diazonium salts with mixtures of formaldehyde and 1,3-diaminopentane". Canadian Journal of Chemistry 83, nr 10 (1.10.2005): 1799–807. http://dx.doi.org/10.1139/v05-192.
Pełny tekst źródłaBergeron, Raymond J., i Howard W. Seligsohn. "Hexahydropyrimidines as masked spermidine vectors in drug delivery". Bioorganic Chemistry 14, nr 4 (grudzień 1986): 345–55. http://dx.doi.org/10.1016/0045-2068(86)90001-5.
Pełny tekst źródłaLUK'YANOV, O. A., G. V. POKHVISNEVA i T. V. TERNIKOVA. "ChemInform Abstract: N,N′-Diacylated Imidazolidines and Hexahydropyrimidines." ChemInform 26, nr 12 (18.08.2010): no. http://dx.doi.org/10.1002/chin.199512067.
Pełny tekst źródłaZELENIN, K. N., V. V. ALEKSEYEV, I. V. UKRAINTSEV i I. V. TSELINSKY. "ChemInform Abstract: 2-Substituted Hexahydropyrimidines and Their Tautomerism." ChemInform 29, nr 24 (22.06.2010): no. http://dx.doi.org/10.1002/chin.199824134.
Pełny tekst źródłaKatritzky, Alan R., Sandeep K. Singh i Hai-Ying He. "ChemInform Abstract: Novel Syntheses of Hexahydropyrimidines and Tetrahydroquinazolines." ChemInform 33, nr 52 (18.05.2010): no. http://dx.doi.org/10.1002/chin.200252148.
Pełny tekst źródłaJanati, Fatemeh, Majid M. Heravi i Ahmad Mirshokraie. "Superparamagnetic Iron Oxide as an Efficient Catalyst for the One-Pot, Solvent-Free Synthesis of 5,5-Disubstituted Hexahydropyrimidines and Their Spiro Analogues". Journal of Chemistry 2013 (2013): 1–5. http://dx.doi.org/10.1155/2013/214617.
Pełny tekst źródłaKNABE, J., i J. BIWERSI. "ChemInform Abstract: Racemates and Enantiomers of 5,5-Disubstituted Hexahydropyrimidines." ChemInform 25, nr 16 (19.08.2010): no. http://dx.doi.org/10.1002/chin.199416191.
Pełny tekst źródłaGöblyös, Anikó, László Lázár i Ferenc Fülöp. "Ring-chain tautomerism of 2-aryl-substituted-hexahydropyrimidines and tetrahydroquinazolines". Tetrahedron 58, nr 5 (styczeń 2002): 1011–16. http://dx.doi.org/10.1016/s0040-4020(01)01196-6.
Pełny tekst źródłaAhmed, Nayeem, Saima Tarannum i Zeba N. Siddiqui. "Dy/chitosan: a highly efficient and recyclable heterogeneous nano catalyst for the synthesis of hexahydropyrimidines in aqueous media". RSC Advances 5, nr 63 (2015): 50691–700. http://dx.doi.org/10.1039/c5ra08160b.
Pełny tekst źródłaTolpygin, I. E. "Chemosensor activity of 2-(anthracen-9-yl)-substituted imidazolidines and hexahydropyrimidines". Russian Journal of Organic Chemistry 48, nr 1 (styczeń 2012): 104–8. http://dx.doi.org/10.1134/s1070428012010162.
Pełny tekst źródłaGarratt, Peter J., Simon N. Thorn i Roger Wrigglesworth. "Regioselective and enantiospecific synthesis of 6-substituted and 5,6-disubstituted hexahydropyrimidines". Tetrahedron Letters 32, nr 5 (styczeń 1991): 691–94. http://dx.doi.org/10.1016/s0040-4039(00)74861-1.
Pełny tekst źródłaSosnovskikh, V. Ya, i V. A. Kutsenko. "Synthesis of 2-(2-hydroxyaroylmethylene)hexahydropyrimidines from 2-trichloromethylchromones and trimethylenediamine". Russian Chemical Bulletin 48, nr 11 (listopad 1999): 2117–20. http://dx.doi.org/10.1007/bf02494859.
Pełny tekst źródłaKorbonits, Dezsö, Erzsébet Tóbiás-Héja i Pαl Kolonits. "Ring – Chain Tautomerism of 4-Hydroximino-hexahydropyrimidines Substituted in Position 2". Chemische Berichte 124, nr 5 (maj 1991): 1199–202. http://dx.doi.org/10.1002/cber.19911240536.
Pełny tekst źródłaZhou, Hui, Hetti Handi Chaminda Lakmal, Jonathan M. Baine, Henry U. Valle, Xue Xu i Xin Cui. "Catalytic [2 + 2 + 2] cycloaddition with indium(iii)-activated formaldimines: a practical and selective access to hexahydropyrimidines and 1,3-diamines from alkenes". Chemical Science 8, nr 9 (2017): 6520–24. http://dx.doi.org/10.1039/c7sc02576a.
Pełny tekst źródłaLatypova, D. R. "Mannich-Type Reaction for Synthesis of Hexahydropyrimidines and 3,7-Diazabicyclo[3.3.1]Nonanes". Bashkir chemistry journal 25, nr 2 (sierpień 2018): 10. http://dx.doi.org/10.17122/bcj-2018-2-10-23.
Pełny tekst źródłaLorente, Antonio, José L. Garacia Navio, José C. Lopez Perez i José L. Soto. "A Simple Synthesis of 4-Amino-6-aryl-2-thioxotetra-and -hexahydropyrimidines". Synthesis 1985, nr 01 (1985): 89–92. http://dx.doi.org/10.1055/s-1985-31121.
Pełny tekst źródłaShakirov, R. R., T. V. Dokichev, R. Z. Biglova, N. M. Vlasova, N. Z. Baibulatova i R. F. Talipov. "Methyl nitroacetate and 3-nitropropionate in the synthesis of hexahydropyrimidines and piperidines". Chemistry of Heterocyclic Compounds 44, nr 1 (styczeń 2008): 43–49. http://dx.doi.org/10.1007/s10593-008-0011-y.
Pełny tekst źródłaPokhvisneva, G. V., i O. A. Luk’yanov. "Synthesis of 2-substituted 1-tosyl-3-(1-tosyliminoalkyl)imidazolidines and-hexahydropyrimidines". Russian Chemical Bulletin 55, nr 5 (maj 2006): 903–6. http://dx.doi.org/10.1007/s11172-006-0350-8.
Pełny tekst źródłaKALYANAM, N., P. C. PARTHASARATHY, L. ANANTHAN, S. G. MANJUNATHA i M. A. LIKHATE. "ChemInform Abstract: Studies on Antiamoebic Compounds. Part 4. Synthesis of Hexahydropyrimidines and Tetrahydroimidazoles." ChemInform 23, nr 28 (21.08.2010): no. http://dx.doi.org/10.1002/chin.199228071.
Pełny tekst źródłaZohdi, Hussein F., Nora M. Rateb i Sherif M. Elnagdy. "Green synthesis and antimicrobial evaluation of some new trifluoromethyl-substituted hexahydropyrimidines by grinding". European Journal of Medicinal Chemistry 46, nr 11 (listopad 2011): 5636–40. http://dx.doi.org/10.1016/j.ejmech.2011.09.036.
Pełny tekst źródłaHwang, Jong Yeon, Hee-Young Kim, Suyeon Jo, Eunjung Park, Jihyun Choi, Sunju Kong, Dong-Sik Park i in. "Synthesis and evaluation of hexahydropyrimidines and diamines as novel hepatitis C virus inhibitors". European Journal of Medicinal Chemistry 70 (grudzień 2013): 315–25. http://dx.doi.org/10.1016/j.ejmech.2013.09.055.
Pełny tekst źródłaSosnovskikh, V. Ya, i V. A. Kutsenko. "ChemInform Abstract: Synthesis of 2-(2-Hydroxyaroylmethylene)hexahydropyrimidines from 2-Trichloromethylchromones and Trimethylenediamine." ChemInform 31, nr 14 (9.06.2010): no. http://dx.doi.org/10.1002/chin.200014136.
Pełny tekst źródłaGARRATT, P. J., S. N. THORN i R. WRIGGLESWORTH. "ChemInform Abstract: Regioselective and Enantiospecific Synthesis of 6-Substituted and 5,6- Disubstituted Hexahydropyrimidines." ChemInform 22, nr 50 (22.08.2010): no. http://dx.doi.org/10.1002/chin.199150159.
Pełny tekst źródłaTolpygin, I. E. "ChemInform Abstract: Chemosensor Activity of 2-(Anthracen-9-yl)-Substituted Imidazolidines and Hexahydropyrimidines." ChemInform 43, nr 29 (21.06.2012): no. http://dx.doi.org/10.1002/chin.201229176.
Pełny tekst źródłaKORBONITS, D., E. TOBIAS-HEJA i P. KOLONITS. "ChemInform Abstract: Ring-Chain Tautomerism of 4-Hydroximino-hexahydropyrimidines Substituted in Position 2." ChemInform 22, nr 31 (22.08.2010): no. http://dx.doi.org/10.1002/chin.199131084.
Pełny tekst źródłaKORBONITS, D., E. TOBIAS-HEJA, K. SIMON i P. KOLONITS. "ChemInform Abstract: Solvent-Dependent Reversible Rearrangement of 4-(Hydroxyimino) hexahydropyrimidines to 4-Aminotetrahydropyrimidine 3-Oxides." ChemInform 25, nr 20 (19.08.2010): no. http://dx.doi.org/10.1002/chin.199420072.
Pełny tekst źródłaOrelli, Liliana R., María B. García, Isabel A. Perillo, Loris Tonidandel i Pietro Traldi. "A comparison of the electron ionization and electrospray behaviour of some N,N′-disubstituted hexahydropyrimidines". Rapid Communications in Mass Spectrometry 20, nr 5 (7.02.2006): 823–28. http://dx.doi.org/10.1002/rcm.2375.
Pełny tekst źródłaSubramaniyan, Vasudevan, Ashok Kumar, Anbarasu Govindaraj i Ganesan Mani. "Crystal structure and DFT analyses of a pentacoordinated PCP pincer nickel(II) complex". Acta Crystallographica Section C Structural Chemistry 75, nr 6 (21.05.2019): 734–39. http://dx.doi.org/10.1107/s2053229619006211.
Pełny tekst źródłaKireeva, D. R., i A. I. Kamalova. "Synthesis of Hexahydropyrimidines and 1,2,3,4-Tetrahydropyridines by Reaction of Ethyl Benzoylacetate with Formaldehyde and Primary Amines". Russian Journal of Organic Chemistry 56, nr 10 (październik 2020): 1733–37. http://dx.doi.org/10.1134/s1070428020100103.
Pełny tekst źródłaBerges, David A., Jianmei Fan, Sylvie Devinck i Kendall Mower. "Preference for AxialN-Alkylation of Tetrahydro-1,3-oxazines and Hexahydropyrimidines: Manifestation of a Kinetic Anomeric Effect". Journal of Organic Chemistry 65, nr 3 (luty 2000): 889–94. http://dx.doi.org/10.1021/jo991752i.
Pełny tekst źródłaDandia, Anshu, Anuj K. Jain i Sonam Sharma. "Indium triflate catalyzed one-pot multicomponent synthesis of spiro-hexahydropyrimidines explained by multiple covalent bond formation". Tetrahedron Letters 53, nr 39 (wrzesień 2012): 5270–74. http://dx.doi.org/10.1016/j.tetlet.2012.07.079.
Pełny tekst źródłaMaloshitskaya, Olga, Jari Sinkkonen, Vladimir V. Ovcharenko, Kirill N. Zelenin i Kalevi Pihlaja. "Chain-ring-chain tautomerism in 2-aryl-substituted hexahydropyrimidines and 1H-2,3-dihydroperimidines. Does it appear?" Tetrahedron 60, nr 32 (sierpień 2004): 6913–21. http://dx.doi.org/10.1016/j.tet.2004.05.092.
Pełny tekst źródłaShephard, MJ, i MN Paddonrow. "A Caveat Concerning the Use of the AM1 and PM3 Semiempirical Methods in Calculating Conformational Preferences in Acyclic Amines and Saturated Azaheterocycles". Australian Journal of Chemistry 46, nr 4 (1993): 547. http://dx.doi.org/10.1071/ch9930547.
Pełny tekst źródłaBesse, Richard, Peter J. Garratt, Christopher J. Hobbs, Helen M. Rogers, A. Mannan Sueleiman, Christopher S.J. Walpole i Roger Wrigglesworth. "Ring size preference in the intramolecular cyclisation of amines with esters. Synthesis of aminoacid derived hexahydropyrimidines and tetrahydroimidazoles". Tetrahedron 46, nr 23 (styczeń 1990): 7803–12. http://dx.doi.org/10.1016/s0040-4020(01)90077-8.
Pełny tekst źródłaKar, Purabi, Aparajita Nayak, Y. P. Bhoi i B. G. Mishra. "Preparation and catalytic application of sulfonated PVA-Zr-pillared clay nanocomposite materials towards one pot synthesis of hexahydropyrimidines". Microporous and Mesoporous Materials 223 (marzec 2016): 176–86. http://dx.doi.org/10.1016/j.micromeso.2015.11.006.
Pełny tekst źródłaDandia, Anshu, Anuj K. Jain i Sonam Sharma. "ChemInform Abstract: Indium Triflate Catalyzed One-Pot Multicomponent Synthesis of Spiro-Hexahydropyrimidines Explained by Multiple Covalent Bond Formation." ChemInform 44, nr 2 (8.01.2013): no. http://dx.doi.org/10.1002/chin.201302147.
Pełny tekst źródłaHuang, Zhi-Tang, Wei-Xing Gan i Xiao-Jun Wang. "Synthesis and X-ray structure analysis of 2-[cyano(aryl)-methylene]-imidazolidines, -hexahydropyrimidines, and -hexahydro-1H-1,3-diazepines". Journal f�r Praktische Chemie 330, nr 5 (1988): 724–34. http://dx.doi.org/10.1002/prac.19883300507.
Pełny tekst źródłaAhmed, Nayeem, Saima Tarannum i Zeba N. Siddiqui. "ChemInform Abstract: Dy/Chitosan: A Highly Efficient and Recyclable Heterogeneous Nano Catalyst for the Synthesis of Hexahydropyrimidines in Aqueous Media." ChemInform 46, nr 44 (15.10.2015): no. http://dx.doi.org/10.1002/chin.201544187.
Pełny tekst źródłaSaraswathi, K., M. Suresh i A. Pandurangan. "Synthesis, Hirshfeld surface analysis, spectral investigations, DFT calculations, ADME studies and molecular docking of Hexahydropyrimidines derivative against dimeric Apolipoprotein A-IV". Journal of Molecular Structure 1255 (maj 2022): 132447. http://dx.doi.org/10.1016/j.molstruc.2022.132447.
Pełny tekst źródłaBESSE, R., P. J. GARRATT, C. J. HOBBS, H. M. ROGERS, A. M. SUELEIMAN, C. S. J. WALPOLE i R. WRIGGLESWORTH. "ChemInform Abstract: Ring Size Preference in the Intramolecular Cyclisation of Amines with Esters. Synthesis of Amino Acid Derived Hexahydropyrimidines and Tetrahydroimidazoles." ChemInform 22, nr 9 (23.08.2010): no. http://dx.doi.org/10.1002/chin.199109085.
Pełny tekst źródłaPalermo, Valeria, Ángel Sathicq, Thierry Constantieux, Jean Rodríguez, Patricia Vázquez i Gustavo Romanelli. "New Vanadium Keggin Heteropolyacids Encapsulated in a Silica Framework: Recyclable Catalysts for the Synthesis of Highly Substituted Hexahydropyrimidines Under Suitable Conditions". Catalysis Letters 145, nr 4 (19.02.2015): 1022–32. http://dx.doi.org/10.1007/s10562-015-1498-3.
Pełny tekst źródłaHuang, Zhi-tang, i Zhi-rong Liu. "Synthesis of 2-(Benzoylmethylene)imidazolidines and -hexahydropyrimidines by Condensation of Ethyl Benzoylacetimidates With 1,2-Ethanediamine or 1,3-Propandiamine, and Some Addition Reactions". Synthesis 1987, nr 04 (1987): 357–62. http://dx.doi.org/10.1055/s-1987-27942.
Pełny tekst źródłaIshar, M. P., Gurmit Singh i Gurpinder Singh. "An Efficient Route to Novel 2-(Salicylmethylidine)imidazolidines and (Salicylmethylidene)hexahydropyrimidines through Reactions of 2-(N-Methylanilino)-3-formylchromone with Aliphatic Diamines". Synlett, nr 2 (2003): 0256–58. http://dx.doi.org/10.1055/s-2003-36780.
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