Academic literature on the topic '[3.3.0]furofuranone'
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 '[3.3.0]furofuranone.'
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 "[3.3.0]furofuranone":
Peng, Xiao-Shui, Ridge Michael P. Ylagan, Yuk Ming Siu, and Henry N. C. Wong. "Synthesis and Application of [3.3.0]Furofuranone in Total Synthesis." Chemistry - An Asian Journal 10, no. 10 (July 20, 2015): 2070–83. http://dx.doi.org/10.1002/asia.201500288.
Peng, Xiao-Shui, Ridge Michael P. Ylagan, Yuk Ming Siu, and Henry N. C. Wong. "ChemInform Abstract: Synthesis and Application of [3.3.0]Furofuranone in Total Synthesis." ChemInform 46, no. 46 (October 27, 2015): no. http://dx.doi.org/10.1002/chin.201546255.
Kojic, Vesna, Milos Svircev, Sanja Djokic, Ivana Kovacevic, Marko Rodic, Bojana Sreco-Zelenovic, Velimir Popsavin, and Mirjana Popsavin. "Synthesis and antiproliferative activity of new thiazole hybrids with [3.3.0]furofuranone or tetrahydrofuran scaffolds." Journal of the Serbian Chemical Society, no. 00 (2023): 2. http://dx.doi.org/10.2298/jsc221130002k.
Ariztia, Julen, Alicia Chateau, Cédric Boura, Claude Didierjean, Sandrine Lamandé-Langle, and Nadia Pellegrini Moïse. "Synthesis of anti-proliferative [3.3.0]furofuranone derivatives by lactonization and functionalization of C-glycosyl compounds." Bioorganic & Medicinal Chemistry 45 (September 2021): 116313. http://dx.doi.org/10.1016/j.bmc.2021.116313.
Rios, María Y., Yordin D. Ocampo-Acuña, M. Ángeles Ramírez-Cisneros, and María E. Salazar-Rios. "Furofuranone Lignans from Leucophyllum ambiguum." Journal of Natural Products 83, no. 5 (April 2, 2020): 1424–31. http://dx.doi.org/10.1021/acs.jnatprod.9b00759.
Swain, Nigel A., Richard C. D. Brown, and Gordon Bruton. "An efficient synthesis of endo,exo-furofuranone derivatives." Chemical Communications, no. 18 (August 13, 2002): 2042–43. http://dx.doi.org/10.1039/b206150c.
Marchand, Patrice A., Norman G. Lewis, and Jaroslav Zajicek. "Oxygen insertion in Sesamumindicum furanofuran lignans. Diastereoselective syntheses of enzyme substrate analogues." Canadian Journal of Chemistry 75, no. 6 (June 1, 1997): 840–49. http://dx.doi.org/10.1139/v97-102.
Zhang, Wen, Lingzi Li, and 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, no. 17 (2021): 9430–42. http://dx.doi.org/10.1039/d0cs01471k.
Yates, Peter, D. Jean Burnell, Vernon J. Freer, and Jeffery F. Sawyer. "Synthesis of cedranoid sesquiterpenes. III. Functionalization at carbon 4." Canadian Journal of Chemistry 65, no. 1 (January 1, 1987): 69–77. http://dx.doi.org/10.1139/v87-012.
Yates, Peter, Rupinder S. Grewal, Peter C. Hayes, and Jeffery F. Sawyer. "Synthesis of cedranoid sesquiterpenes. V. The biotols." Canadian Journal of Chemistry 66, no. 11 (November 1, 1988): 2805–15. http://dx.doi.org/10.1139/v88-434.
Dissertations / Theses on the topic "[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.
Hewitt, 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.
Atalar, 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.
Bennett, 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.
Pazinatto, 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.
In 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.
Spieler, 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.
Jacquet, 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.
Pisoni, 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.
This 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.
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. .
Books on the topic "[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.
Bennett, Lisa Ruth. Enantioselective synthetic approaches tp natural products based on functionalised CIS-bicyclo[3.3.0]octane synthons. Salford: University of Salford, 1995.
Freer, Vernon John. The synthesis of bicyclo (3.3.0) octane derivatives related to the biotols. 1985.
Book chapters on the topic "[3.3.0]furofuranone":
Whitesell, James K., and Mark A. Minton. "Bicyclo[3.3.0]octanes." In 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.
"2-Oxa-4-azabicyclo[3.3.0]oct-3-ene to 3,7-Diferrabicyclo[3.3.0]oct-1(5)-ene." In Substance Index, edited by Backes, Fröhlich, and Padeken. Stuttgart: Georg Thieme Verlag, 2000. http://dx.doi.org/10.1055/b-0035-114015.
"5-Ethyl-3,7-dioxa-1-azabicyclo[3.3.0]octan." In Gesundheitsschädliche Arbeitsstoffe, 1–4. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527603441.ch34.
"2,4,6-Trioxabicyclo[3.3.0]octane to Thieno[3,4-d]-1,3-dithiol-1-ium." In Substance Index, edited by Backes, Fröhlich, and Padeken. Stuttgart: Georg Thieme Verlag, 2000. http://dx.doi.org/10.1055/b-0035-114016.
"4λ6,8,9-Trithiabicyclo[5.2.0]non-1(7)-ene to Bicyclo[3.3.0]octa-1,3-diene." In Substance Index, edited by Backes, Fröhlich, and Padeken. Stuttgart: Georg Thieme Verlag, 2000. http://dx.doi.org/10.1055/b-0035-114012.
"Bicyclo[3.3.0]octa-1(5),2-diene to Bicyclo[2.2.1]heptan-7-ium." In Substance Index, edited by Backes, Fröhlich, and Padeken. Stuttgart: Georg Thieme Verlag, 2000. http://dx.doi.org/10.1055/b-0035-114013.
"Bicyclo[2.2.1]heptane-2,5-bis[ium] to 2-Oxa-4-azabicyclo[3.3.0]octane." In Substance Index, edited by Backes, Fröhlich, and Padeken. Stuttgart: Georg Thieme Verlag, 2000. http://dx.doi.org/10.1055/b-0035-114014.
"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." In Substance Index, edited by Backes, Fröhlich, and Padeken. Stuttgart: Georg Thieme Verlag, 2000. http://dx.doi.org/10.1055/b-0035-114018.
Conference papers on the topic "[3.3.0]furofuranone":
Levovnik, Bojan D., Aleksa P. Alargić, Miloš M. Svirčev, and Goran I. Benedeković. "Building a 3D QSAR model with isopropylidene analogs of cytotoxic styryl-lactones." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.559l.
Потапов, К. В., М. А. Новиков, Р. А. Новиков, and Ю. В. Томилов. "КАТАЛИТИЧЕСКИЙ ЭНАНТИОСЕЛЕКТИВНЫЙ СИНТЕЗ 1,2-ДИАЗАБИЦИКЛО[3.3.0]-ОКТАНОВ. ФОРМАЛЬНОЕ [3+2]-ЦИКЛОПРИСОЕДИНЕНИЕ ДАЦ К ПИРАЗОЛИНАМ." In MedChem-Russia 2021. Издательство Волгоградского государственного медицинского университета, 2022. http://dx.doi.org/10.19163/medchemrussia2021-2022-23.
Tanase, Constantin, Constantin Draghici, and 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." In The 24th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2020. http://dx.doi.org/10.3390/ecsoc-24-08390.
Reports on the topic "[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, May 2008. http://dx.doi.org/10.21236/ada486096.
Stevens, E. D., J. H. Boyer, C. M. Lau, I. R. Politzer, and K. Tangaraj. Bimanes (1,5-Diazabicyclo(3.3.0)Octadiendiones). Laser Activity in syn- Bimanes. Fort Belvoir, VA: Defense Technical Information Center, May 1990. http://dx.doi.org/10.21236/ada222800.