Artykuły w czasopismach na temat „Spiro compound”
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DANSHPAJUH, Marjan, i 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, nr 1-2 (17.01.2023): 61–74. http://dx.doi.org/10.33224/rrch.2023.68.1-2.06.
Pełny tekst źródłaTripathi, Rahul R., i 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 (wrzesień 2013): 119–25. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.15.119.
Pełny tekst źródłaTripathi, Rahul R., i 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 (29.06.2013): 119–25. http://dx.doi.org/10.56431/p-h7k957.
Pełny tekst źródłaHafez, Hend N., Abdel-Rhman B. A. El-Gazzar i Magdi E. A. Zaki. "Simple approach to thieno[3,2-d]pyrimidines as new scaffolds of antimicrobial activities". Acta Pharmaceutica 66, nr 3 (1.09.2016): 331–51. http://dx.doi.org/10.1515/acph-2016-0029.
Pełny tekst źródłaMacháček, Vladimír, Makky M. M. Hassanien i 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, nr 9 (1987): 2225–40. http://dx.doi.org/10.1135/cccc19872225.
Pełny tekst źródłaNakano, Koji, Ko Takase i Keiichi Noguchi. "Furan-Containing Chiral Spiro-Fused Polycyclic Aromatic Compounds: Synthesis and Photophysical Properties". Molecules 27, nr 16 (11.08.2022): 5103. http://dx.doi.org/10.3390/molecules27165103.
Pełny tekst źródłaKonyar, Dilan, Cenk A. Andac i Erdem Buyukbingol. "Design, Synthesis and Cytotoxic Activity of Spiro(oxindole-3-3'- pyrrolidine) Derivatives". Letters in Drug Design & Discovery 15, nr 1 (3.01.2018): 37–45. http://dx.doi.org/10.2174/1570180814666170810120634.
Pełny tekst źródłaBarakat, Assem, Mohammad Shahidul Islam, M. Ali, Abdullah Mohammed Al-Majid, Saeed Alshahrani, Abdullah Saleh Alamary, Sammer Yousuf i M. Iqbal Choudhary. "Regio- and Stereoselective Synthesis of a New Series of Spirooxindole Pyrrolidine Grafted Thiochromene Scaffolds as Potential Anticancer Agents". Symmetry 13, nr 8 (4.08.2021): 1426. http://dx.doi.org/10.3390/sym13081426.
Pełny tekst źródłaWestphal, Regina, Eclair Venturini Filho, Laiza Bruzadelle Loureiro, Cláudio Francisco Tormena, Claudia Pessoa, Celina de Jesus Guimarães, Mariana Palmeira Manso i in. "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, nr 22 (19.11.2022): 8051. http://dx.doi.org/10.3390/molecules27228051.
Pełny tekst źródłaWu, Mengyao, Yilin Wang, Xiaojun Tan i 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, nr 9 (2020): 1175–84. http://dx.doi.org/10.2298/jsc191217026w.
Pełny tekst źródłaWang, Yilin, Mengyao Wu, Xiaojun Tan i Jinsong Gu. "Insights into the reaction mechanism between phosphacyclopropenylidene and methyleneimine: A theoretical study". Main Group Chemistry 19, nr 3 (14.10.2020): 237–44. http://dx.doi.org/10.3233/mgc-200906.
Pełny tekst źródłaShukla, Paritosh, Ashok Sharma, Leena Fageria i 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, nr 2 (12.03.2019): 257–67. http://dx.doi.org/10.2174/1573407213666170828165512.
Pełny tekst źródłaRys, Paul, Ruth Weber i Qinglan Wu. "Light-induced change of the molecular charge in a spironaphthoxazine compound". Canadian Journal of Chemistry 71, nr 11 (1.11.1993): 1828–33. http://dx.doi.org/10.1139/v93-228.
Pełny tekst źródłaKim, Seung Hyun, Sang Hyun Sung, Soo Young Choi, Young Keun Chung, Jinwoong Kim i Young Choong Kim. "Idesolide: A New Spiro Compound fromIdesiapolycarpa". Organic Letters 7, nr 15 (lipiec 2005): 3275–77. http://dx.doi.org/10.1021/ol051105f.
Pełny tekst źródłaTada, Masahiro, Masashi Nagai, Chieko Okumura, Yasuko Osano i Takao Matsuzaki. "Novel Spiro-Compound, Hyperolactone fromHypericum chinenseL." Chemistry Letters 18, nr 4 (kwiecień 1989): 683–86. http://dx.doi.org/10.1246/cl.1989.683.
Pełny tekst źródłaFlefel, Eman M., Walaa I. El-Sofany, Reem A. K. Al-Harbi i Mahmoud El-Shahat. "Development of a Novel Series of Anticancer and Antidiabetic: Spirothiazolidines Analogs". Molecules 24, nr 13 (9.07.2019): 2511. http://dx.doi.org/10.3390/molecules24132511.
Pełny tekst źródłaSepsey Für, Csilla, i Hedvig Bölcskei. "New Spiro[cycloalkane-pyridazinone] Derivatives with Favorable Fsp3 Character". Chemistry 2, nr 4 (6.10.2020): 837–48. http://dx.doi.org/10.3390/chemistry2040055.
Pełny tekst źródłaSong, Fuhang, Rui Lin, Na Yang, Jia Jia, Shangzhu Wei, Jiahui Han, Jiangpeng Li, Hongkai Bi i Xiuli Xu. "Antibacterial Secondary Metabolites from Marine-Derived Fungus Aspergillus sp. IMCASMF180035". Antibiotics 10, nr 4 (3.04.2021): 377. http://dx.doi.org/10.3390/antibiotics10040377.
Pełny tekst źródłaMohamed, Magda F., Amr Mohamed Abdelmoniem, Ahmed H. M. Elwahy i 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, nr 4 (6.04.2018): 372–81. http://dx.doi.org/10.2174/1568009617666170630143311.
Pełny tekst źródłaBernet, Bruno, Paul M. Bishop, Maurice Caron, Takeshi Kawamata, Bernard L. Roy, Luc Ruest, Gilles Sauvé, Pierre Soucy i 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, nr 10 (1.10.1985): 2814–18. http://dx.doi.org/10.1139/v85-469.
Pełny tekst źródłaKotha, Sambasivarao, Mohammad Saifuddin, Rashid Ali i Gaddamedi Sreevani. "Spiro annulation of cage polycycles via Grignard reaction and ring-closing metathesis as key steps". Beilstein Journal of Organic Chemistry 11 (5.08.2015): 1367–72. http://dx.doi.org/10.3762/bjoc.11.147.
Pełny tekst źródłaMacháček, Vladimír, Makky M. M. Hassanien, Vojeslav Štěrba i 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, nr 9 (1986): 1972–85. http://dx.doi.org/10.1135/cccc19861972.
Pełny tekst źródłaSayed, Hayam, Hebat-Allah Abbas, Eman Morsi, Abd Amr i Nayera Abdelwahad. "Antimicrobial activity of some synthesized glucopyranosyl-pyrimidine carbonitrile and fused pyrimidine systems". Acta Pharmaceutica 60, nr 4 (1.12.2010): 479–91. http://dx.doi.org/10.2478/v10007-010-0033-8.
Pełny tekst źródłaMaihesuti, L., P. Lan, M. Imerhasan, K. A. Eshbakova i X. Jia. "A New Spiro Compound from Caragana acanthophylla". Chemistry of Natural Compounds 53, nr 4 (lipiec 2017): 646–48. http://dx.doi.org/10.1007/s10600-017-2081-5.
Pełny tekst źródłaSilva, 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 i in. "Antitumor Effect of a Novel Spiro-Acridine Compound is Associated with Up-Regulation of Th1-Type Responses and Antiangiogenic Action". Molecules 25, nr 1 (20.12.2019): 29. http://dx.doi.org/10.3390/molecules25010029.
Pełny tekst źródłaEl-Ossaily, Y. A. B., R. M. Zaki i S. A. Metwally. "Investigation and Synthesis of Some Novel Spiro Heterocycles Related to Indoline Moiety". Journal of Scientific Research 6, nr 2 (22.04.2014): 293–307. http://dx.doi.org/10.3329/jsr.v6i2.17590.
Pełny tekst źródłaWang, Guisheng, Yilin Yuan, Zhaokun Li, Junhao Zhu, Zhigang She i Yan Chen. "Cytosporones with Anti-Inflammatory Activities from the Mangrove Endophytic Fungus Phomopsis sp. QYM-13". Marine Drugs 21, nr 12 (7.12.2023): 631. http://dx.doi.org/10.3390/md21120631.
Pełny tekst źródłaTourneur, P., F. Lucas, C. Quinton, Y. Olivier, R. Lazzaroni, P. Viville, J. Cornil i 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, nr 41 (2020): 14462–68. http://dx.doi.org/10.1039/d0tc03285a.
Pełny tekst źródłaGovindan, E., PanneerSelvam Yuvaraj, Boreddy Siva Rami Reddy, K. Premalatha i 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, nr 2 (18.01.2014): o173. http://dx.doi.org/10.1107/s1600536814000191.
Pełny tekst źródłaMohamed, Abou-El-Hamd H., Ali K. Khalafallah i Afifi H. Yousof. "Biotransformation of Glabratephrin, a Rare Type of Isoprenylated Flavonoids, by Aspergillus niger". Zeitschrift für Naturforschung C 63, nr 7-8 (1.08.2008): 561–64. http://dx.doi.org/10.1515/znc-2008-7-816.
Pełny tekst źródłaSchaefer, W. P., i J. Abulū. "An Indanyl Precursor to a Chiral Spiro Compound". Acta Crystallographica Section C Crystal Structure Communications 51, nr 11 (15.11.1995): 2364–66. http://dx.doi.org/10.1107/s0108270195005609.
Pełny tekst źródłaSchaefer, W. P., L. M. Henling, H. C. McBay i J. Abulū. "A Pinacol Precursor to a Chiral Spiro Compound". Acta Crystallographica Section C Crystal Structure Communications 52, nr 1 (15.01.1996): 104–7. http://dx.doi.org/10.1107/s0108270195010213.
Pełny tekst źródłaAugustine, T., V. Ramkumar, S. Arul Antony i 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, nr 11 (26.10.2007): o4412. http://dx.doi.org/10.1107/s1600536807051264.
Pełny tekst źródłaKuznetsova, Juliana V., Varvara T. Tkachenko, Lada M. Petrovskaya, Maria E. Filkina, Dmitry E. Shybanov, Yuri K. Grishin, Vitaly A. Roznyatovsky i in. "[3+2]-Cycloaddition of Nitrile Imines to Parabanic Acid Derivatives—An Approach to Novel Spiroimidazolidinediones". International Journal of Molecular Sciences 25, nr 1 (19.12.2023): 18. http://dx.doi.org/10.3390/ijms25010018.
Pełny tekst źródłaGuan, Zong, Jan C. Namyslo, Martin H. H. Drafz, Martin Nieger i Andreas Schmidt. "Dimerisation, rhodium complex formation and rearrangements of N-heterocyclic carbenes of indazoles". Beilstein Journal of Organic Chemistry 10 (10.04.2014): 832–40. http://dx.doi.org/10.3762/bjoc.10.79.
Pełny tekst źródłaHu, Bin-Yuan, Da-Peng Qin, Shao-Xiang Wang, Jing-Jing Qi i Yong-Xian Cheng. "Novel Terpenoids with Potent Cytotoxic Activities from Resina Commiphora". Molecules 23, nr 12 (7.12.2018): 3239. http://dx.doi.org/10.3390/molecules23123239.
Pełny tekst źródłaBando, Masayoshi, Yuki Mizukami, Kiyohiko Nakajima, Zhiyi Song i Tamotsu Takahashi. "Formation of a spiro compound via coupling of a cyclopentadienyl ligand with a diene moiety of titanacyclopentadiene". Dalton Transactions 46, nr 47 (2017): 16408–11. http://dx.doi.org/10.1039/c7dt03789a.
Pełny tekst źródłaSharma, Sakshi, Goutam Brahmachari, Rajni Kant i 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, nr 3 (13.05.2016): 335–43. http://dx.doi.org/10.1107/s2052520616005060.
Pełny tekst źródłaTong, Junjie, Yang Zhang, Yang Xu, Yangyang Han, Chuan Li, Wenying Zhuang i Yongsheng Che. "Spirocitrinols A and B, citrinin derivatives with a spiro[chromane-2,3′-isochromane] skeleton from Penicillium citrinum". RSC Advances 13, nr 9 (2023): 6124–29. http://dx.doi.org/10.1039/d3ra00665d.
Pełny tekst źródłaRether, Jan, Gerhard Erkel, Timm Anke i Olov Sterner. "Inhibition of inducible TNF-α expression by oxaspirodion, a novel spiro-compound from the ascomycete Chaetomium subspirale". Biological Chemistry 385, nr 9 (1.09.2004): 829–34. http://dx.doi.org/10.1515/bc.2004.108.
Pełny tekst źródłaTan, Xiaojun, i 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, nr 3 (2019): 293–301. http://dx.doi.org/10.2298/jsc180603072t.
Pełny tekst źródłaLutz, Marlon R., Matthias Zeller i 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, nr 11 (24.10.2007): o4390—o4391. http://dx.doi.org/10.1107/s1600536807051136.
Pełny tekst źródłaZhang, Xiu-Ling, Ai-Zhen Liu i 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, nr 7 (23.06.2006): o2961—o2962. http://dx.doi.org/10.1107/s1600536806022847.
Pełny tekst źródłaMa, Xican, Bing Han, Aoyu Wang, Lu Yang, Menghao Huang, Kushan Chowdhury, Jian Gu, Kai Zhang i Kai Lv. "Identification of benzothiazones containing a hexahydropyrrolo[3,4-c]pyrrol moiety as antitubercular agents against MDR-MTB". RSC Advances 10, nr 24 (2020): 14410–14. http://dx.doi.org/10.1039/d0ra00750a.
Pełny tekst źródłavan der Haas, Richard, Jeroen Dekker, Jorma Hassfeld, Anastasia Hager, Peter Fey, Philipp Rubenbauer i Eric Damen. "Synthesis and Properties of 2-Oxa-6-azaspiro[3.3]heptane Sulfonate Salts". Synthesis 49, nr 11 (2.03.2017): 2394–401. http://dx.doi.org/10.1055/s-0036-1588733.
Pełny tekst źródłaSennikova, Valeriia V., Alena V. Zalaltdinova, Yulia M. Sadykova, Ayrat R. Khamatgalimov, Almir S. Gazizov, Alexandra D. Voloshina, Anna P. Lyubina i in. "Diastereoselective Synthesis of Novel Spiro-Phosphacoumarins and Evaluation of Their Anti-Cancer Activity". International Journal of Molecular Sciences 23, nr 22 (18.11.2022): 14348. http://dx.doi.org/10.3390/ijms232214348.
Pełny tekst źródłaZhang, Yu-Hua, Xiao-Hui Wang, Shan Liu i 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, nr 7 (9.06.2006): o2620—o2621. http://dx.doi.org/10.1107/s1600536806020605.
Pełny tekst źródłaVrábel, Viktor, Július Sivý, Ľubomír Švorc, Jan Světlík i Šafař Peter. "Crystal and electronic structure, N–H⋯N and C–H⋯O interactions in novel spiro-[chroman-chromene]-carboxylate". Acta Chimica Slovaca 10, nr 1 (25.04.2017): 74–78. http://dx.doi.org/10.1515/acs-2017-0013.
Pełny tekst źródłaDastoorani, Parvaneh, Mohammad A. Khalilzadeh, Fatemeh Khaleghi, Malek Taher Maghsoodlou, Werner Kaminsky i Ali Shokuhi Rad. "Experimental and computational studies on the synthesis of diastereoselective natural-based Meldrum spiro dibenzofuran derivatives". New Journal of Chemistry 43, nr 17 (2019): 6615–21. http://dx.doi.org/10.1039/c9nj00766k.
Pełny tekst źródłaEngelhardt, Udo, i 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, nr 5 (1.05.1989): 612–14. http://dx.doi.org/10.1515/znb-1989-0518.
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