Artículos de revistas sobre el tema "Spiro compound"
Crea una cita precisa en los estilos APA, MLA, Chicago, Harvard y otros
Consulte los 50 mejores artículos de revistas para su investigación sobre el tema "Spiro compound".
Junto a cada fuente en la lista de referencias hay un botón "Agregar a la bibliografía". Pulsa este botón, y generaremos automáticamente la referencia bibliográfica para la obra elegida en el estilo de cita que necesites: APA, MLA, Harvard, Vancouver, Chicago, etc.
También puede descargar el texto completo de la publicación académica en formato pdf y leer en línea su resumen siempre que esté disponible en los metadatos.
Explore artículos de revistas sobre una amplia variedad de disciplinas y organice su bibliografía correctamente.
DANSHPAJUH, Marjan y Neda HASANZADEH. "Study of influence of anomeric effect on conformational preferences using hybrid density functional theory (DFT) and natural bond orbital (NBO) interpretation". Revue Roumaine de Chimie 68, n.º 1-2 (17 de enero de 2023): 61–74. http://dx.doi.org/10.33224/rrch.2023.68.1-2.06.
Texto completoTripathi, Rahul R. y Ratnamala P. Sonawane. "An Extraction of the Isatin from the Couroupita guianesis (Cannon Ball Tree) and a Novel Synthesis of the N,N'-(2-oxo-3'H-spiro[indoline-3,2'-[1,3,4]thiadiazole]-3',5'-diyl]diacetamidefrom the Isatin". International Letters of Chemistry, Physics and Astronomy 15 (septiembre de 2013): 119–25. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.15.119.
Texto completoTripathi, Rahul R. y Ratnamala P. Sonawane. "An Extraction of the Isatin from the <i>Couroupita guianesis</i> (Cannon Ball Tree) and a Novel Synthesis of the N,N'-(2-oxo-3'H-spiro[indoline-3,2'-[1,3,4]thiadiazole]-3',5'-diyl]diacetamidefrom the Isatin". International Letters of Chemistry, Physics and Astronomy 15 (29 de junio de 2013): 119–25. http://dx.doi.org/10.56431/p-h7k957.
Texto completoHafez, Hend N., Abdel-Rhman B. A. El-Gazzar y Magdi E. A. Zaki. "Simple approach to thieno[3,2-d]pyrimidines as new scaffolds of antimicrobial activities". Acta Pharmaceutica 66, n.º 3 (1 de septiembre de 2016): 331–51. http://dx.doi.org/10.1515/acph-2016-0029.
Texto completoMacháček, Vladimír, Makky M. M. Hassanien y Vojeslav Štěrba. "Kinetics and mechanism of spiro adduct formation from and smiles rearrangement of N-methyl-N-(2,4,6-trinitrophenyl)aminoacetanilide. Base-catalyzed transformation of N-(2,4,6-trinitrophenylamino)acetanilide into 2-nitroso-4,6-dinitroaniline". Collection of Czechoslovak Chemical Communications 52, n.º 9 (1987): 2225–40. http://dx.doi.org/10.1135/cccc19872225.
Texto completoNakano, Koji, Ko Takase y Keiichi Noguchi. "Furan-Containing Chiral Spiro-Fused Polycyclic Aromatic Compounds: Synthesis and Photophysical Properties". Molecules 27, n.º 16 (11 de agosto de 2022): 5103. http://dx.doi.org/10.3390/molecules27165103.
Texto completoKonyar, Dilan, Cenk A. Andac y Erdem Buyukbingol. "Design, Synthesis and Cytotoxic Activity of Spiro(oxindole-3-3'- pyrrolidine) Derivatives". Letters in Drug Design & Discovery 15, n.º 1 (3 de enero de 2018): 37–45. http://dx.doi.org/10.2174/1570180814666170810120634.
Texto completoBarakat, Assem, Mohammad Shahidul Islam, M. Ali, Abdullah Mohammed Al-Majid, Saeed Alshahrani, Abdullah Saleh Alamary, Sammer Yousuf y M. Iqbal Choudhary. "Regio- and Stereoselective Synthesis of a New Series of Spirooxindole Pyrrolidine Grafted Thiochromene Scaffolds as Potential Anticancer Agents". Symmetry 13, n.º 8 (4 de agosto de 2021): 1426. http://dx.doi.org/10.3390/sym13081426.
Texto completoWestphal, Regina, Eclair Venturini Filho, Laiza Bruzadelle Loureiro, Cláudio Francisco Tormena, Claudia Pessoa, Celina de Jesus Guimarães, Mariana Palmeira Manso et al. "Green Synthesis of Spiro Compounds with Potential Anticancer Activity through Knoevenagel/Michael/Cyclization Multicomponent Domino Reactions Organocatalyzed by Ionic Liquid and Microwave-Assisted". Molecules 27, n.º 22 (19 de noviembre de 2022): 8051. http://dx.doi.org/10.3390/molecules27228051.
Texto completoWu, Mengyao, Yilin Wang, Xiaojun Tan y Jinsong Gu. "Theoretical study on the reaction between phosphacyclopropenylidene and ethylene: An alternative approach to the formation of phosphorus-bearing heterocyclic compound". Journal of the Serbian Chemical Society 85, n.º 9 (2020): 1175–84. http://dx.doi.org/10.2298/jsc191217026w.
Texto completoWang, Yilin, Mengyao Wu, Xiaojun Tan y Jinsong Gu. "Insights into the reaction mechanism between phosphacyclopropenylidene and methyleneimine: A theoretical study". Main Group Chemistry 19, n.º 3 (14 de octubre de 2020): 237–44. http://dx.doi.org/10.3233/mgc-200906.
Texto completoShukla, Paritosh, Ashok Sharma, Leena Fageria y Rajdeep Chowdhury. "Novel Spiro/non-Spiro Pyranopyrazoles: Eco-Friendly Synthesis, In-vitro Anticancer Activity, DNA Binding, and In-silico Docking Studies". Current Bioactive Compounds 15, n.º 2 (12 de marzo de 2019): 257–67. http://dx.doi.org/10.2174/1573407213666170828165512.
Texto completoRys, Paul, Ruth Weber y Qinglan Wu. "Light-induced change of the molecular charge in a spironaphthoxazine compound". Canadian Journal of Chemistry 71, n.º 11 (1 de noviembre de 1993): 1828–33. http://dx.doi.org/10.1139/v93-228.
Texto completoKim, Seung Hyun, Sang Hyun Sung, Soo Young Choi, Young Keun Chung, Jinwoong Kim y Young Choong Kim. "Idesolide: A New Spiro Compound fromIdesiapolycarpa". Organic Letters 7, n.º 15 (julio de 2005): 3275–77. http://dx.doi.org/10.1021/ol051105f.
Texto completoTada, Masahiro, Masashi Nagai, Chieko Okumura, Yasuko Osano y Takao Matsuzaki. "Novel Spiro-Compound, Hyperolactone fromHypericum chinenseL." Chemistry Letters 18, n.º 4 (abril de 1989): 683–86. http://dx.doi.org/10.1246/cl.1989.683.
Texto completoFlefel, Eman M., Walaa I. El-Sofany, Reem A. K. Al-Harbi y Mahmoud El-Shahat. "Development of a Novel Series of Anticancer and Antidiabetic: Spirothiazolidines Analogs". Molecules 24, n.º 13 (9 de julio de 2019): 2511. http://dx.doi.org/10.3390/molecules24132511.
Texto completoSepsey Für, Csilla y Hedvig Bölcskei. "New Spiro[cycloalkane-pyridazinone] Derivatives with Favorable Fsp3 Character". Chemistry 2, n.º 4 (6 de octubre de 2020): 837–48. http://dx.doi.org/10.3390/chemistry2040055.
Texto completoSong, Fuhang, Rui Lin, Na Yang, Jia Jia, Shangzhu Wei, Jiahui Han, Jiangpeng Li, Hongkai Bi y Xiuli Xu. "Antibacterial Secondary Metabolites from Marine-Derived Fungus Aspergillus sp. IMCASMF180035". Antibiotics 10, n.º 4 (3 de abril de 2021): 377. http://dx.doi.org/10.3390/antibiotics10040377.
Texto completoMohamed, Magda F., Amr Mohamed Abdelmoniem, Ahmed H. M. Elwahy y Ismail A. Abdelhamid. "DNA Fragmentation, Cell Cycle Arrest, and Docking Study of Novel Bis Spiro-cyclic 2-oxindole of Pyrimido[4,5-b]quinoline-4,6-dione Derivatives Against Breast Carcinoma". Current Cancer Drug Targets 18, n.º 4 (6 de abril de 2018): 372–81. http://dx.doi.org/10.2174/1568009617666170630143311.
Texto completoBernet, Bruno, Paul M. Bishop, Maurice Caron, Takeshi Kawamata, Bernard L. Roy, Luc Ruest, Gilles Sauvé, Pierre Soucy y Pierre Deslongchamps. "Formal total synthesis of erythromycin A. Part II. Preparation of a 1,7-dioxaspiro[5.5]undecane derivative of erythronolide A seco acid methyl ester from erythromycin A". Canadian Journal of Chemistry 63, n.º 10 (1 de octubre de 1985): 2814–18. http://dx.doi.org/10.1139/v85-469.
Texto completoKotha, Sambasivarao, Mohammad Saifuddin, Rashid Ali y Gaddamedi Sreevani. "Spiro annulation of cage polycycles via Grignard reaction and ring-closing metathesis as key steps". Beilstein Journal of Organic Chemistry 11 (5 de agosto de 2015): 1367–72. http://dx.doi.org/10.3762/bjoc.11.147.
Texto completoMacháček, Vladimír, Makky M. M. Hassanien, Vojeslav Štěrba y Antonín Lyčka. "Formation of the Meisenheimer spiro adduct of N-(2,4,6-trinitrophenyl)alanine methylamide and its rearrangement to 2-amino-N-methyl-N-(2,4,6-trinitrophenyl)propanamide". Collection of Czechoslovak Chemical Communications 51, n.º 9 (1986): 1972–85. http://dx.doi.org/10.1135/cccc19861972.
Texto completoSayed, Hayam, Hebat-Allah Abbas, Eman Morsi, Abd Amr y Nayera Abdelwahad. "Antimicrobial activity of some synthesized glucopyranosyl-pyrimidine carbonitrile and fused pyrimidine systems". Acta Pharmaceutica 60, n.º 4 (1 de diciembre de 2010): 479–91. http://dx.doi.org/10.2478/v10007-010-0033-8.
Texto completoMaihesuti, L., P. Lan, M. Imerhasan, K. A. Eshbakova y X. Jia. "A New Spiro Compound from Caragana acanthophylla". Chemistry of Natural Compounds 53, n.º 4 (julio de 2017): 646–48. http://dx.doi.org/10.1007/s10600-017-2081-5.
Texto completoSilva, Daiana K. Frade, Sâmia S. Duarte, Thaís M. H. Lisboa, Rafael C. Ferreira, Ana Luíza de O. Lopes, Deyse C. M. Carvalho, Sandra Rodrigues-Mascarenhas et al. "Antitumor Effect of a Novel Spiro-Acridine Compound is Associated with Up-Regulation of Th1-Type Responses and Antiangiogenic Action". Molecules 25, n.º 1 (20 de diciembre de 2019): 29. http://dx.doi.org/10.3390/molecules25010029.
Texto completoEl-Ossaily, Y. A. B., R. M. Zaki y S. A. Metwally. "Investigation and Synthesis of Some Novel Spiro Heterocycles Related to Indoline Moiety". Journal of Scientific Research 6, n.º 2 (22 de abril de 2014): 293–307. http://dx.doi.org/10.3329/jsr.v6i2.17590.
Texto completoWang, Guisheng, Yilin Yuan, Zhaokun Li, Junhao Zhu, Zhigang She y Yan Chen. "Cytosporones with Anti-Inflammatory Activities from the Mangrove Endophytic Fungus Phomopsis sp. QYM-13". Marine Drugs 21, n.º 12 (7 de diciembre de 2023): 631. http://dx.doi.org/10.3390/md21120631.
Texto completoTourneur, P., F. Lucas, C. Quinton, Y. Olivier, R. Lazzaroni, P. Viville, J. Cornil y C. Poriel. "White-light electroluminescence from a layer incorporating a single fully-organic spiro compound with phosphine oxide substituents". Journal of Materials Chemistry C 8, n.º 41 (2020): 14462–68. http://dx.doi.org/10.1039/d0tc03285a.
Texto completoGovindan, E., PanneerSelvam Yuvaraj, Boreddy Siva Rami Reddy, K. Premalatha y A. SubbiahPandi. "(4S)-5′-Chloro-3,7,7-trimethyl-5,6,7,8-tetrahydro-4H-spiro[1,2-oxazolo[5,4-b]quinoline-4,3′-indole]-2′,5-dione". Acta Crystallographica Section E Structure Reports Online 70, n.º 2 (18 de enero de 2014): o173. http://dx.doi.org/10.1107/s1600536814000191.
Texto completoMohamed, Abou-El-Hamd H., Ali K. Khalafallah y Afifi H. Yousof. "Biotransformation of Glabratephrin, a Rare Type of Isoprenylated Flavonoids, by Aspergillus niger". Zeitschrift für Naturforschung C 63, n.º 7-8 (1 de agosto de 2008): 561–64. http://dx.doi.org/10.1515/znc-2008-7-816.
Texto completoSchaefer, W. P. y J. Abulū. "An Indanyl Precursor to a Chiral Spiro Compound". Acta Crystallographica Section C Crystal Structure Communications 51, n.º 11 (15 de noviembre de 1995): 2364–66. http://dx.doi.org/10.1107/s0108270195005609.
Texto completoSchaefer, W. P., L. M. Henling, H. C. McBay y J. Abulū. "A Pinacol Precursor to a Chiral Spiro Compound". Acta Crystallographica Section C Crystal Structure Communications 52, n.º 1 (15 de enero de 1996): 104–7. http://dx.doi.org/10.1107/s0108270195010213.
Texto completoAugustine, T., V. Ramkumar, S. Arul Antony y Charles C. Kanakam. "6′′-Methoxy-1′-methyl-4′-phenylacenaphthene-1-spiro-2′-pyrrolidine-3′-spiro-3′′-chroman-2,4′′-dione". Acta Crystallographica Section E Structure Reports Online 63, n.º 11 (26 de octubre de 2007): o4412. http://dx.doi.org/10.1107/s1600536807051264.
Texto completoKuznetsova, Juliana V., Varvara T. Tkachenko, Lada M. Petrovskaya, Maria E. Filkina, Dmitry E. Shybanov, Yuri K. Grishin, Vitaly A. Roznyatovsky et al. "[3+2]-Cycloaddition of Nitrile Imines to Parabanic Acid Derivatives—An Approach to Novel Spiroimidazolidinediones". International Journal of Molecular Sciences 25, n.º 1 (19 de diciembre de 2023): 18. http://dx.doi.org/10.3390/ijms25010018.
Texto completoGuan, Zong, Jan C. Namyslo, Martin H. H. Drafz, Martin Nieger y Andreas Schmidt. "Dimerisation, rhodium complex formation and rearrangements of N-heterocyclic carbenes of indazoles". Beilstein Journal of Organic Chemistry 10 (10 de abril de 2014): 832–40. http://dx.doi.org/10.3762/bjoc.10.79.
Texto completoHu, Bin-Yuan, Da-Peng Qin, Shao-Xiang Wang, Jing-Jing Qi y Yong-Xian Cheng. "Novel Terpenoids with Potent Cytotoxic Activities from Resina Commiphora". Molecules 23, n.º 12 (7 de diciembre de 2018): 3239. http://dx.doi.org/10.3390/molecules23123239.
Texto completoBando, Masayoshi, Yuki Mizukami, Kiyohiko Nakajima, Zhiyi Song y Tamotsu Takahashi. "Formation of a spiro compound via coupling of a cyclopentadienyl ligand with a diene moiety of titanacyclopentadiene". Dalton Transactions 46, n.º 47 (2017): 16408–11. http://dx.doi.org/10.1039/c7dt03789a.
Texto completoSharma, Sakshi, Goutam Brahmachari, Rajni Kant y Vivek K. Gupta. "One-pot green synthesis of biologically relevant novel spiro[indolin-2-one-3,4′-pyrano[2,3-c]pyrazoles] and studies on their spectral and X-ray crystallographic behaviors". Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 72, n.º 3 (13 de mayo de 2016): 335–43. http://dx.doi.org/10.1107/s2052520616005060.
Texto completoTong, Junjie, Yang Zhang, Yang Xu, Yangyang Han, Chuan Li, Wenying Zhuang y Yongsheng Che. "Spirocitrinols A and B, citrinin derivatives with a spiro[chromane-2,3′-isochromane] skeleton from Penicillium citrinum". RSC Advances 13, n.º 9 (2023): 6124–29. http://dx.doi.org/10.1039/d3ra00665d.
Texto completoRether, Jan, Gerhard Erkel, Timm Anke y Olov Sterner. "Inhibition of inducible TNF-α expression by oxaspirodion, a novel spiro-compound from the ascomycete Chaetomium subspirale". Biological Chemistry 385, n.º 9 (1 de septiembre de 2004): 829–34. http://dx.doi.org/10.1515/bc.2004.108.
Texto completoTan, Xiaojun y Xiuhui Lu. "Ab initio study of the mechanism of formation of a spiro-Sn-heterocyclic ring compound by the cycloaddition reaction of H2C=Sn: and ethylene". Journal of the Serbian Chemical Society 84, n.º 3 (2019): 293–301. http://dx.doi.org/10.2298/jsc180603072t.
Texto completoLutz, Marlon R., Matthias Zeller y Daniel P. Becker. "2,3,5′,6,6′,7-Hexamethoxy-3′H,10H-spiro[anthracene-9,1′-isobenzofuran]-3′,10-dione". Acta Crystallographica Section E Structure Reports Online 63, n.º 11 (24 de octubre de 2007): o4390—o4391. http://dx.doi.org/10.1107/s1600536807051136.
Texto completoZhang, Xiu-Ling, Ai-Zhen Liu y Mei-Fang Jin. "1′-Methyl-4′-(1-naphthyl)-1H-indole-3-spiro-2′-pyrrolidine-3′-spiro-2′′-thiazolo[3,2-a]benzimidazole-2(3H),3′′(2′′H)-dione". Acta Crystallographica Section E Structure Reports Online 62, n.º 7 (23 de junio de 2006): o2961—o2962. http://dx.doi.org/10.1107/s1600536806022847.
Texto completoMa, Xican, Bing Han, Aoyu Wang, Lu Yang, Menghao Huang, Kushan Chowdhury, Jian Gu, Kai Zhang y Kai Lv. "Identification of benzothiazones containing a hexahydropyrrolo[3,4-c]pyrrol moiety as antitubercular agents against MDR-MTB". RSC Advances 10, n.º 24 (2020): 14410–14. http://dx.doi.org/10.1039/d0ra00750a.
Texto completovan der Haas, Richard, Jeroen Dekker, Jorma Hassfeld, Anastasia Hager, Peter Fey, Philipp Rubenbauer y Eric Damen. "Synthesis and Properties of 2-Oxa-6-azaspiro[3.3]heptane Sulfonate Salts". Synthesis 49, n.º 11 (2 de marzo de 2017): 2394–401. http://dx.doi.org/10.1055/s-0036-1588733.
Texto completoSennikova, Valeriia V., Alena V. Zalaltdinova, Yulia M. Sadykova, Ayrat R. Khamatgalimov, Almir S. Gazizov, Alexandra D. Voloshina, Anna P. Lyubina et al. "Diastereoselective Synthesis of Novel Spiro-Phosphacoumarins and Evaluation of Their Anti-Cancer Activity". International Journal of Molecular Sciences 23, n.º 22 (18 de noviembre de 2022): 14348. http://dx.doi.org/10.3390/ijms232214348.
Texto completoZhang, Yu-Hua, Xiao-Hui Wang, Shan Liu y Cheng Yao. "3,9-Bis(2-hydroxy-2-propyl)-2,4,8,10-tetraoxa-3,9-diphosphaspiro[5.5]undecane 3,9-dioxide hemihydrate". Acta Crystallographica Section E Structure Reports Online 62, n.º 7 (9 de junio de 2006): o2620—o2621. http://dx.doi.org/10.1107/s1600536806020605.
Texto completoVrábel, Viktor, Július Sivý, Ľubomír Švorc, Jan Světlík y Šafař Peter. "Crystal and electronic structure, N–H⋯N and C–H⋯O interactions in novel spiro-[chroman-chromene]-carboxylate". Acta Chimica Slovaca 10, n.º 1 (25 de abril de 2017): 74–78. http://dx.doi.org/10.1515/acs-2017-0013.
Texto completoDastoorani, Parvaneh, Mohammad A. Khalilzadeh, Fatemeh Khaleghi, Malek Taher Maghsoodlou, Werner Kaminsky y Ali Shokuhi Rad. "Experimental and computational studies on the synthesis of diastereoselective natural-based Meldrum spiro dibenzofuran derivatives". New Journal of Chemistry 43, n.º 17 (2019): 6615–21. http://dx.doi.org/10.1039/c9nj00766k.
Texto completoEngelhardt, Udo y Ursula Diefenbach. "Notizen: Cyclotriphosphazen-2-spiro-3′ -cyclodi[phosphadiazan] — Eine Spiroverbindung aus Hexachlortriphosphazen und Dihydrazidothiophosphorsäure-O-phenylester / Cyclotriphosphazene-2-spiro-3′-cyclodi[phosphadiazane] — A Spiro Compound from Hexachlorocyclotriphosphazene and Dihydrazidothiophosphoric Acid 0-Phenylester". Zeitschrift für Naturforschung B 44, n.º 5 (1 de mayo de 1989): 612–14. http://dx.doi.org/10.1515/znb-1989-0518.
Texto completo