Literatura académica sobre el tema "[3.3.0]furofuranone"
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Artículos de revistas sobre el tema "[3.3.0]furofuranone"
Peng, Xiao-Shui, Ridge Michael P. Ylagan, Yuk Ming Siu y Henry N. C. Wong. "Synthesis and Application of [3.3.0]Furofuranone in Total Synthesis". Chemistry - An Asian Journal 10, n.º 10 (20 de julio de 2015): 2070–83. http://dx.doi.org/10.1002/asia.201500288.
Texto completoPeng, Xiao-Shui, Ridge Michael P. Ylagan, Yuk Ming Siu y Henry N. C. Wong. "ChemInform Abstract: Synthesis and Application of [3.3.0]Furofuranone in Total Synthesis". ChemInform 46, n.º 46 (27 de octubre de 2015): no. http://dx.doi.org/10.1002/chin.201546255.
Texto completoKojic, Vesna, Milos Svircev, Sanja Djokic, Ivana Kovacevic, Marko Rodic, Bojana Sreco-Zelenovic, Velimir Popsavin y Mirjana Popsavin. "Synthesis and antiproliferative activity of new thiazole hybrids with [3.3.0]furofuranone or tetrahydrofuran scaffolds". Journal of the Serbian Chemical Society, n.º 00 (2023): 2. http://dx.doi.org/10.2298/jsc221130002k.
Texto completoAriztia, Julen, Alicia Chateau, Cédric Boura, Claude Didierjean, Sandrine Lamandé-Langle y Nadia Pellegrini Moïse. "Synthesis of anti-proliferative [3.3.0]furofuranone derivatives by lactonization and functionalization of C-glycosyl compounds". Bioorganic & Medicinal Chemistry 45 (septiembre de 2021): 116313. http://dx.doi.org/10.1016/j.bmc.2021.116313.
Texto completoRios, María Y., Yordin D. Ocampo-Acuña, M. Ángeles Ramírez-Cisneros y María E. Salazar-Rios. "Furofuranone Lignans from Leucophyllum ambiguum". Journal of Natural Products 83, n.º 5 (2 de abril de 2020): 1424–31. http://dx.doi.org/10.1021/acs.jnatprod.9b00759.
Texto completoSwain, Nigel A., Richard C. D. Brown y Gordon Bruton. "An efficient synthesis of endo,exo-furofuranone derivatives". Chemical Communications, n.º 18 (13 de agosto de 2002): 2042–43. http://dx.doi.org/10.1039/b206150c.
Texto completoMarchand, Patrice A., Norman G. Lewis y Jaroslav Zajicek. "Oxygen insertion in Sesamumindicum furanofuran lignans. Diastereoselective syntheses of enzyme substrate analogues". Canadian Journal of Chemistry 75, n.º 6 (1 de junio de 1997): 840–49. http://dx.doi.org/10.1139/v97-102.
Texto completoZhang, Wen, Lingzi Li y Chuang-Chuang Li. "Synthesis of natural products containing highly strained trans-fused bicyclo[3.3.0]octane: historical overview and future prospects". Chemical Society Reviews 50, n.º 17 (2021): 9430–42. http://dx.doi.org/10.1039/d0cs01471k.
Texto completoYates, Peter, D. Jean Burnell, Vernon J. Freer y Jeffery F. Sawyer. "Synthesis of cedranoid sesquiterpenes. III. Functionalization at carbon 4". Canadian Journal of Chemistry 65, n.º 1 (1 de enero de 1987): 69–77. http://dx.doi.org/10.1139/v87-012.
Texto completoYates, Peter, Rupinder S. Grewal, Peter C. Hayes y Jeffery F. Sawyer. "Synthesis of cedranoid sesquiterpenes. V. The biotols". Canadian Journal of Chemistry 66, n.º 11 (1 de noviembre de 1988): 2805–15. http://dx.doi.org/10.1139/v88-434.
Texto completoTesis sobre el tema "[3.3.0]furofuranone"
Dubbert, Robert Allen. "Iron carbonyl assisted cyclocarbonylation of 1,6-enynes to bicyclo(3.3.0)octenones". Case Western Reserve University School of Graduate Studies / OhioLINK, 1993. http://rave.ohiolink.edu/etdc/view?acc_num=case1060615827.
Texto completoHewitt, Jacqueline Diane. "Enantioselective preparation of cis-bicycolo[3.3.0]octane derivatives using chiral lithium amide bases". Thesis, University of Salford, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.292871.
Texto completoAtalar, Taner. "Synthetic Strategy Directed Towards The Synthesis Of Bicyclo[3.3.0]octa-3,5,8-triene-2,7-dione". Master's thesis, METU, 2004. http://etd.lib.metu.edu.tr/upload/12605089/index.pdf.
Texto completoBennett, Lisa Ruth. "Enantioselective synthetic approaches to natural products based on functionalised cis-bicyclo[3.3.0]octane synthons". Thesis, University of Salford, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.262622.
Texto completoPazinatto, Mariane. "Síntese de compostos 4-azabiciclo[3.3.0]octano intermediários avançados para a preparação de alcalóides hiacintacina". reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2012. http://hdl.handle.net/10183/37802.
Texto completoIn this work it was developed a short and convergent route for obtention of 4- azabicyclo[3.3.0]octane skeleton, advanced intermediates that possesses all existent carbons in the structure of hiacintacine pirrolizidinic alkaloids. Initially Michael reactions between activated alkynes and proline ethyl ester were performed, in mild conditions, leading to enaminocarbonylic adducts stereoselectively for isomer E, with yields higher than 80%. Further reduction of these enaminocarbonyl compounds, by hydrogenation or hydride addition, furnished the corresponding aminodiesters with yields between 75 and 85%. For the (2S)-1-benziloximethyl-3-ethoxi-3- oxopropylpirrolidine-2-ethyl carboxylate reduction has shown to be stereoselective in a 3:1 ratio. These aminodiesters were submitted to Dieckmann condensations through two distinct methodologies: using metallic sodium in refluxing THF, and with potassium hydride at ambient temperature, affording the obtention of bicyclic enolesters, with yields between 60 and 65%. In parallel, reduction reactions with LiAlH4 of these aminodiesters were performed leading to obtention of the corresponding diols, with yields between 75 and 80%. An a-hydroxyester was obtained from oxidation of the bicyclic enolester promoted by CeCl3.7H2O, in 95% yield. The importance of this methodology is the fact that it provided the insertion of an hydroxyl group in the a-ester position, a substituent present in the target compounds.
Mannchen, Fabian [Verfasser]. "Übergangsmetall-katalysierte Vinylcyclopropan-Umlagerung und Studien zur Struktur-Wirkungsbeziehung von Bicyclo[3.3.0]octan-Derivaten / Fabian Mannchen". München : Verlag Dr. Hut, 2015. http://d-nb.info/1075409160/34.
Texto completoSpieler, Jan. "Synthese chiraler Liganden mit [3.3.0]- und [3.3.1]-bicyclischem Grundgerüst und ihre Anwendung in der enantioselektiven Übergangsmetall-Katalyse". [S.l. : s.n.], 2000. http://deposit.ddb.de/cgi-bin/dokserv?idn=961741309.
Texto completoJacquet, Fabienne. "Obtention de l'hydroxy-4 dioxa-2,6 bicyclo (3.3.0) octanone-8 (1S,4S,5R) par voie catalytique, et selon un procédé d'électrosynthèse organique". Grenoble 2 : ANRT, 1986. http://catalogue.bnf.fr/ark:/12148/cb37598417t.
Texto completoPisoni, Diego dos Santos. "Preparação e funcionalização da (5R)-4,8-dimetilbiciclo[3.3.0]octa-1(8),3-dien-2-ona: um bloco de construção para a síntese de terpenóides". reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2006. http://hdl.handle.net/10183/24007.
Texto completoThis work describes the enantioselective preparation of (5R)-4,8-dimethylbicyclo[3.3.0]oct-1(8),3-dien-2-one (128) from (-)-limonene oxide (127). This compound holds the prospect of serving as useful building block or intermediate to prepare a variety of compounds having a bicyclo[3.3.0]octane framework. The key step is the conversion of the chiral aldehyde 163 to bicyclic cyanohydrin 165, through intramolecular alkylation of cyanohydrin TMS eter 164, according to Strok-Takahashi protocol. The stereoselective hydrogenation of dienone 128 led to monosaturated product 20, which is a important intermediate on the ent-kelsoene preparation. Also, catalytic hydrogenation of the two carbon-carbon double bonds of 128, produced 129a, which is a intermediate to formal synthesis of iridoid cis,cis-dihydronepetalactone 13. Further, a new methodology to allylic chlorination of terminal olefins which employ InCl3 in the presence of NaClO was developed. This method was applied to different compounds and furnished allylic chlorides in satisfactory yields.
鍾慧容. "Synthesis of 2,3,7-triazabicyclp[3.3.0]oct-2-enes and 2,3,7-triazabicyclo[3.3.0]oct-3-ene derivatives". Thesis, 1997. http://ndltd.ncl.edu.tw/handle/34001478867006978412.
Texto completo中原大學
化學學系
85
Michael addition and Substitution reaction of 1-methoxycarbonyl-2,3,7-triaza bicyclo[3.3.0]oct-2-enes 2a to electron-deficient dipolarphiles(vinyl ketone、ester)、 alkyl halides , give 7-substituted 1- methoxycarbonyl-2,3,7-triaza bicyclo[3.3.0]oct-2-enes 5. 6. in good yields. Furthermore, 1-methoxycarbonyl-2,3,7-triaza bicyclo[3.3.0] oct-3-enes 7. 8. 9. , are prepared by isomerization of 1-methoxycarbonyl-2,3,7-triaza bicyclo[3.3.0]oct-2-enes 2. 5. 6. .
Libros sobre el tema "[3.3.0]furofuranone"
Hewitt, Jacqueline Diane. Enantioselective preparation of CIS-Bicyclo [3.3.0] octane derivatives using chiral lithium amide bases. Salford: University of Salford, 1990.
Buscar texto completoBennett, Lisa Ruth. Enantioselective synthetic approaches tp natural products based on functionalised CIS-bicyclo[3.3.0]octane synthons. Salford: University of Salford, 1995.
Buscar texto completoFreer, Vernon John. The synthesis of bicyclo (3.3.0) octane derivatives related to the biotols. 1985.
Buscar texto completoCapítulos de libros sobre el tema "[3.3.0]furofuranone"
Whitesell, James K. y Mark A. Minton. "Bicyclo[3.3.0]octanes". En Stereochemical Analysis of Alicyclic Compounds by C-13 NMR Spectroscopy, 137–50. Dordrecht: Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3161-9_13.
Texto completo"2-Oxa-4-azabicyclo[3.3.0]oct-3-ene to 3,7-Diferrabicyclo[3.3.0]oct-1(5)-ene". En Substance Index, editado por Backes, Fröhlich y Padeken. Stuttgart: Georg Thieme Verlag, 2000. http://dx.doi.org/10.1055/b-0035-114015.
Texto completo"5-Ethyl-3,7-dioxa-1-azabicyclo[3.3.0]octan". En Gesundheitsschädliche Arbeitsstoffe, 1–4. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527603441.ch34.
Texto completo"2,4,6-Trioxabicyclo[3.3.0]octane to Thieno[3,4-d]-1,3-dithiol-1-ium". En Substance Index, editado por Backes, Fröhlich y Padeken. Stuttgart: Georg Thieme Verlag, 2000. http://dx.doi.org/10.1055/b-0035-114016.
Texto completo"4λ6,8,9-Trithiabicyclo[5.2.0]non-1(7)-ene to Bicyclo[3.3.0]octa-1,3-diene". En Substance Index, editado por Backes, Fröhlich y Padeken. Stuttgart: Georg Thieme Verlag, 2000. http://dx.doi.org/10.1055/b-0035-114012.
Texto completo"Bicyclo[3.3.0]octa-1(5),2-diene to Bicyclo[2.2.1]heptan-7-ium". En Substance Index, editado por Backes, Fröhlich y Padeken. Stuttgart: Georg Thieme Verlag, 2000. http://dx.doi.org/10.1055/b-0035-114013.
Texto completo"Bicyclo[2.2.1]heptane-2,5-bis[ium] to 2-Oxa-4-azabicyclo[3.3.0]octane". En Substance Index, editado por Backes, Fröhlich y Padeken. Stuttgart: Georg Thieme Verlag, 2000. http://dx.doi.org/10.1055/b-0035-114014.
Texto completo"3-Oxa-6,7,8-triazabicyclo[3.3.0]oct-6-ene to 5H-1,2,3-Triazolo[4,5-c]-1λ4,2,5-thiadiazole". En Substance Index, editado por Backes, Fröhlich y Padeken. Stuttgart: Georg Thieme Verlag, 2000. http://dx.doi.org/10.1055/b-0035-114018.
Texto completoActas de conferencias sobre el tema "[3.3.0]furofuranone"
Levovnik, Bojan D., Aleksa P. Alargić, Miloš M. Svirčev y Goran I. Benedeković. "Building a 3D QSAR model with isopropylidene analogs of cytotoxic styryl-lactones". En 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.559l.
Texto completoПотапов, К. В., М. А. Новиков, Р. А. Новиков y Ю. В. Томилов. "КАТАЛИТИЧЕСКИЙ ЭНАНТИОСЕЛЕКТИВНЫЙ СИНТЕЗ 1,2-ДИАЗАБИЦИКЛО[3.3.0]-ОКТАНОВ. ФОРМАЛЬНОЕ [3+2]-ЦИКЛОПРИСОЕДИНЕНИЕ ДАЦ К ПИРАЗОЛИНАМ". En MedChem-Russia 2021. Издательство Волгоградского государственного медицинского университета, 2022. http://dx.doi.org/10.19163/medchemrussia2021-2022-23.
Texto completoTanase, Constantin, Constantin Draghici y Miron Theodor Caproiu. "Key Intermediates for introducing a bulky bicyclo[3.3.0]heptane skeleton in the w-side chain to reduce the enzyme inactivation of prostaglandins". En The 24th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2020. http://dx.doi.org/10.3390/ecsoc-24-08390.
Texto completoInformes sobre el tema "[3.3.0]furofuranone"
Moore, John B. Stereocontrolled Additions to a Rigid Bicyclo [3.3.0] Octane Ring System. Fort Belvoir, VA: Defense Technical Information Center, mayo de 2008. http://dx.doi.org/10.21236/ada486096.
Texto completoStevens, E. D., J. H. Boyer, C. M. Lau, I. R. Politzer y K. Tangaraj. Bimanes (1,5-Diazabicyclo(3.3.0)Octadiendiones). Laser Activity in syn- Bimanes. Fort Belvoir, VA: Defense Technical Information Center, mayo de 1990. http://dx.doi.org/10.21236/ada222800.
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