Artigos de revistas sobre o tema "[3.3.0]furofuranone"
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Peng, Xiao-Shui, Ridge Michael P. Ylagan, Yuk Ming Siu e 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 julho de 2015): 2070–83. http://dx.doi.org/10.1002/asia.201500288.
Texto completo da fontePeng, Xiao-Shui, Ridge Michael P. Ylagan, Yuk Ming Siu e Henry N. C. Wong. "ChemInform Abstract: Synthesis and Application of [3.3.0]Furofuranone in Total Synthesis". ChemInform 46, n.º 46 (27 de outubro de 2015): no. http://dx.doi.org/10.1002/chin.201546255.
Texto completo da fonteKojic, Vesna, Milos Svircev, Sanja Djokic, Ivana Kovacevic, Marko Rodic, Bojana Sreco-Zelenovic, Velimir Popsavin e 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 completo da fonteAriztia, Julen, Alicia Chateau, Cédric Boura, Claude Didierjean, Sandrine Lamandé-Langle e Nadia Pellegrini Moïse. "Synthesis of anti-proliferative [3.3.0]furofuranone derivatives by lactonization and functionalization of C-glycosyl compounds". Bioorganic & Medicinal Chemistry 45 (setembro de 2021): 116313. http://dx.doi.org/10.1016/j.bmc.2021.116313.
Texto completo da fonteRios, María Y., Yordin D. Ocampo-Acuña, M. Ángeles Ramírez-Cisneros e 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 completo da fonteSwain, Nigel A., Richard C. D. Brown e 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 completo da fonteMarchand, Patrice A., Norman G. Lewis e Jaroslav Zajicek. "Oxygen insertion in Sesamumindicum furanofuran lignans. Diastereoselective syntheses of enzyme substrate analogues". Canadian Journal of Chemistry 75, n.º 6 (1 de junho de 1997): 840–49. http://dx.doi.org/10.1139/v97-102.
Texto completo da fonteZhang, Wen, Lingzi Li e 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 completo da fonteYates, Peter, D. Jean Burnell, Vernon J. Freer e Jeffery F. Sawyer. "Synthesis of cedranoid sesquiterpenes. III. Functionalization at carbon 4". Canadian Journal of Chemistry 65, n.º 1 (1 de janeiro de 1987): 69–77. http://dx.doi.org/10.1139/v87-012.
Texto completo da fonteYates, Peter, Rupinder S. Grewal, Peter C. Hayes e Jeffery F. Sawyer. "Synthesis of cedranoid sesquiterpenes. V. The biotols". Canadian Journal of Chemistry 66, n.º 11 (1 de novembro de 1988): 2805–15. http://dx.doi.org/10.1139/v88-434.
Texto completo da fonteDelamere, C., C. Jakins e E. Lewars. "Tests for aromaticity applied to the pentalenoquinones A computational study". Canadian Journal of Chemistry 79, n.º 10 (1 de outubro de 2001): 1492–504. http://dx.doi.org/10.1139/v01-164.
Texto completo da fonteGuthrie, J. Peter, Roger T. Gallant e Michael C. Jennings. "Preparation and characterization of bicyclic amide acetals and monothioacetals". Canadian Journal of Chemistry 82, n.º 2 (1 de fevereiro de 2004): 268–78. http://dx.doi.org/10.1139/v03-204.
Texto completo da fonteRiaz, Muhammad, Nisar Ullah, Arshad Mehmood, Hafiz Rab Nawaz, Abdul Malik e Nighat Afza. "Furanoid and Furofuranoid Lignans from Daphne oleoides". Zeitschrift für Naturforschung B 55, n.º 12 (1 de dezembro de 2000): 1216–20. http://dx.doi.org/10.1515/znb-2000-1217.
Texto completo da fonteYu, Zhi-Xiang, e Cheng-Hang Liu. "Rh(I)-Catalyzed Intramolecular [3+2] Cycloaddition of trans-2-Allene-Vinylcyclopropanes". Synlett 29, n.º 06 (18 de janeiro de 2018): 764–68. http://dx.doi.org/10.1055/s-0037-1609199.
Texto completo da fonteTănase, Constantin I., Constantin Drăghici e Miron Teodor Caproiu. "New β-ketophosphonates for the synthesis of prostaglandin analogues. 2 Phosphonates with bicyclo[3.3.0]octene and bicyclo[3.3.0]octane scaffolds linked to the β-keto group". New Journal of Chemistry 44, n.º 46 (2020): 20405–10. http://dx.doi.org/10.1039/d0nj04594b.
Texto completo da fonteRobertson, Jeremy, e Kiri Stevens. "Pyrrolizidine alkaloids". Nat. Prod. Rep. 31, n.º 12 (2014): 1721–88. http://dx.doi.org/10.1039/c4np00055b.
Texto completo da fonteDeslongchamps, Ghislain, Daniel Mink, Paul D. Boyle e Nina Singh. "Unusual Weiss–Cook condensation of dimethyl 2,3-dioxobutanedioate and dimethyl 3-oxoglutarate". Canadian Journal of Chemistry 72, n.º 4 (1 de abril de 1994): 1162–64. http://dx.doi.org/10.1139/v94-148.
Texto completo da fonteKrech, Friedrich, Babett Krauss, Adolf Zschunke e Clemens Mügge. "Cis-1-phosphabicyclo[3.3.0]octan". Zeitschrift für anorganische und allgemeine Chemie 629, n.º 9 (agosto de 2003): 1475–76. http://dx.doi.org/10.1002/zaac.200300096.
Texto completo da fonteGimazetdinov, Airat M., Aidar Z. Al’mukhametov e Mansur S. Miftakhov. "Development of a new approach for the synthesis of (+)-15-deoxy-Δ12,14-prostaglandin J2 methyl ester based on the [2+2]-cycloadduct of 5-trimethylsilylcyclopentadiene and dichloroketene". New Journal of Chemistry 46, n.º 14 (2022): 6708–14. http://dx.doi.org/10.1039/d2nj01003h.
Texto completo da fonteRobertson, Jeremy, e Kiri Stevens. "Pyrrolizidine alkaloids: occurrence, biology, and chemical synthesis". Natural Product Reports 34, n.º 1 (2017): 62–89. http://dx.doi.org/10.1039/c5np00076a.
Texto completo da fonteAntoniadis, Greg A., Michael T. M. Clements, Sriyawathie Peiris e J. B. Stothers. "13C magnetic resonance studies. 131. An examination of β-enolization in an unsaturated [3.2.1] system: 3,3-dimethylbicyclo[3.2.1]oct-6-en-2-one". Canadian Journal of Chemistry 65, n.º 7 (1 de julho de 1987): 1557–62. http://dx.doi.org/10.1139/v87-262.
Texto completo da fonteAurich, Hans Günter, e Michael Soeberdt. "Darstellung enantiomerenreiner 3-Oxa-2,7-diazabicyclo[3.3.0]octane und ihre Umwandlung in andere bicyclische Ringsysteme/Preparation of Pure Enantiomeric 3-Oxa-2,7-diazabicyclo[3.3.0]octanes and their Conversion to Other Bicyclic Ring-Systems". Zeitschrift für Naturforschung B 54, n.º 1 (1 de janeiro de 1999): 87–95. http://dx.doi.org/10.1515/znb-1999-0117.
Texto completo da fonteBrandstätter, Marco, Nikolas Huwyler e Erick M. Carreira. "Gold(i)-catalyzed stereoselective cyclization of 1,3-enyne aldehydes by a 1,3-acyloxy migration/Nazarov cyclization/aldol addition cascade". Chemical Science 10, n.º 35 (2019): 8219–23. http://dx.doi.org/10.1039/c9sc02828e.
Texto completo da fonteBhat, Bilal A., Showkat Rashid e Goverdhan Mehta. "Progress in the Total Synthesis of Natural Products Embodying Diverse Furofuranone Motifs: A New Millennium Update". Asian Journal of Organic Chemistry 9, n.º 11 (13 de outubro de 2020): 1726–53. http://dx.doi.org/10.1002/ajoc.202000401.
Texto completo da fonteFlippen-Anderson, Judith L., Jeffrey R. Deschamps, Clifford George e Richard D. Gilardi. "4,4,8,8-Tetranitro-2,6-dioxabicyclo[3.3.0]octane". Acta Crystallographica Section E Structure Reports Online 58, n.º 9 (23 de agosto de 2002): o1018—o1020. http://dx.doi.org/10.1107/s1600536802014101.
Texto completo da fonteBaumeister, U., H. Hartung e F. Krech. "1-Phosphabicyclo[3.3.0]octane 1-sulfide". Acta Crystallographica Section C Crystal Structure Communications 46, n.º 4 (15 de abril de 1990): 634–37. http://dx.doi.org/10.1107/s0108270189008085.
Texto completo da fonteEberle, Marcel K., Reinhart Keese e Helen Stoeckli-Evans. "A bicyclo[3.3.0]octan-2-ylcyclopentanone". Acta Crystallographica Section E Structure Reports Online 57, n.º 5 (30 de abril de 2001): o461—o462. http://dx.doi.org/10.1107/s1600536801006808.
Texto completo da fonteMa, Chenxi, e Anthony F. Hill. "Methimazolyl based diptych bicyclo-[3.3.0]-ruthenaboratranes". Dalton Transactions 48, n.º 6 (2019): 1976–92. http://dx.doi.org/10.1039/c8dt04813d.
Texto completo da fonteXiang, Yuejun, Raymond F. Schinazi e Kang Zhao. "Synthesis of [3.3.0] bicyclic isoxazolidinyl nucleosides". Bioorganic & Medicinal Chemistry Letters 6, n.º 13 (julho de 1996): 1475–78. http://dx.doi.org/10.1016/s0960-894x(96)00262-4.
Texto completo da fonteVega, Andrés, Oscar Donoso-Tauda, Andres Ibañez e Carlos A. Escobar. "Five bicyclo[3.3.0]octa-2,6-dienes". Acta Crystallographica Section C Crystal Structure Communications 64, n.º 4 (8 de março de 2008): o199—o204. http://dx.doi.org/10.1107/s0108270108004290.
Texto completo da fonteKnotnerus, J., e H. Schilling. "Bicyclanes: V. New syntheses of cis-bicyclo[3.3.0]octane and cis-bicyclo[3.3.0]oct-2-ene". Recueil des Travaux Chimiques des Pays-Bas 83, n.º 11 (2 de setembro de 2010): 1185–90. http://dx.doi.org/10.1002/recl.19640831110.
Texto completo da fonteMuhit, Md Abdul, Kaoru Umehara e Hiroshi Noguchi. "Five furofuranone lignan glucosides from Terminalia citrina inhibit in vitro E 2 -enhanced breast cancer cell proliferation". Fitoterapia 113 (setembro de 2016): 74–79. http://dx.doi.org/10.1016/j.fitote.2016.07.004.
Texto completo da fonteGund, Machhindra, Martin Déry e Claude Spino. "Synthesis of carotol using a formal (4+1)-cycloaddition of chiral dialkoxycarbenes". Canadian Journal of Chemistry 96, n.º 3 (março de 2018): 311–27. http://dx.doi.org/10.1139/cjc-2017-0594.
Texto completo da fonteGrygorenko, Oleksandr, Yevhenii Sokolenko, Eugeniy Ostapchuk e Artem Artemenko. "An Approach to 3-Oxa-7-azabicyclo[3.3.0]octanes – Bicyclic Morpholine Surrogates". Synthesis 49, n.º 14 (13 de abril de 2017): 3112–17. http://dx.doi.org/10.1055/s-0036-1588785.
Texto completo da fonteTanase, Constantin I., Anamaria Hanganu e Constantin Draghici. "Trifluoroacetylation of Alcohols During NMR Study of Compounds with Bicyclo[2.2.1]heptane, Oxabicyclo[3.3.0]octane and Bicyclo[3.3.0]octane Skeleton". Revista de Chimie 72, n.º 2 (7 de maio de 2021): 156–77. http://dx.doi.org/10.37358/rc.21.2.8428.
Texto completo da fonteQuast, Helmut, Jürgen Carlsen, Thomas Herkert, Rolf Janiak, Horst Röschert, Eva-Maria Peters, Karl Peters e Hans Georg von Schnering. "Stereochemie der Addition von Phenylmetall-Reagenzien an Bicyclo[3.3.0]octandione und -octadiendione. — Synthese phenylsubstituierter Bicyclo[3.3.0]octadiene". Liebigs Annalen der Chemie 1992, n.º 5 (19 de maio de 1992): 495–511. http://dx.doi.org/10.1002/jlac.199219920188.
Texto completo da fonteBecheanu, Armand, Thomas Bell, Sabine Laschat, Angelika Baro, Wolfgang Frey, Nelli Steinke e Peter Fischer. "Synthesis of Pentalene Systems Employing a Sequence of Pauson-Khand Reaction, Michael Reaction, and Desilylation". Zeitschrift für Naturforschung B 61, n.º 5 (1 de maio de 2006): 589–96. http://dx.doi.org/10.1515/znb-2006-0514.
Texto completo da fonteKliegel, Wolfgang, Gottfried Lubkowitz, Steven J. Rettig e James Trotter. "Structural studies of organoboron compounds. LIII. N,N-Diethylhydroxylamine-(O-B)1,7-dimethyl-3,5-diphenyl-2,4,6-trioxa-7-aza-1-azonia-3-bora-5- boratabicyclo[3.3.0]octane". Canadian Journal of Chemistry 70, n.º 7 (1 de julho de 1992): 2022–26. http://dx.doi.org/10.1139/v92-254.
Texto completo da fonteBird, C. W., E. C. J. Coffee e B. W. C. Schmidl. "Bicyclo [3.3.0]Octane Derivatives for Carbaprostacyclin Synthesis". Synthetic Communications 23, n.º 5 (1 de março de 1993): 613–20. http://dx.doi.org/10.1080/00397919308009819.
Texto completo da fonteLachaise, I., K. Nohair, M. Hakiki e J. Y. Nédélec. "A Straightforward Synthesis of [3.3.0]Bicyclic Compounds". Synthetic Communications 25, n.º 22 (novembro de 1995): 3529–36. http://dx.doi.org/10.1080/00397919508015487.
Texto completo da fonteArchibald, T. G., e K. Baum. "Synthesis of Polynitro-2,6-dioxabicyclo[3.3.0]octanes". Synthetic Communications 19, n.º 9-10 (junho de 1989): 1493–98. http://dx.doi.org/10.1080/00397918908051042.
Texto completo da fonteTanaka, Koichi, Tomoyuki Watanabe e Masako Kato. "Guest-Dependent Organic Photochromism of 7-Bromo-1,4,8-Triphenyl-2,3-Benzo[3.3.0]Octa-2,4,7-Trien-6-One in the Solid State". Journal of Chemical Research 2003, n.º 9 (setembro de 2003): 535–37. http://dx.doi.org/10.3184/030823403322597207.
Texto completo da fonteBartmann, Wilhelm, Gerhard Beck, Wolfram Fehlhaber e Jiří Protiva. "Synthese von (8RS,9SR,11RS,13E,15R)-(±)-1,2,3,4-tetranor-9,11,15-trihydroxy-16,16-dimethyl-18-oxa-13-prostensäure". Collection of Czechoslovak Chemical Communications 54, n.º 1 (1989): 189–95. http://dx.doi.org/10.1135/cccc19890189.
Texto completo da fonteStachel, Hans-Dietrich, Želmíra Odlerová e Karel Waisser. "A New Pharmacophore of Potential Antimycobacterial Activity: The Disulfide Group in the Ring of Alicyclic Compounds". Collection of Czechoslovak Chemical Communications 62, n.º 3 (1997): 510–15. http://dx.doi.org/10.1135/cccc19970510.
Texto completo da fonteButcher, Ray J., Robin Evans e R. Gilardi. "2,4,6-Trinitro-2,4,6,8-tetraazabicyclo[3.3.0]octan-7-one". Acta Crystallographica Section E Structure Reports Online 60, n.º 9 (21 de agosto de 2004): o1543—o1545. http://dx.doi.org/10.1107/s160053680401880x.
Texto completo da fonteCronan Jnr, J. M., F. R. Fronczek e M. L. McLaughlin. "A bichromophoric difulvene from 3,7-bicyclo[3.3.0]octadione". Acta Crystallographica Section C Crystal Structure Communications 46, n.º 6 (15 de junho de 1990): 1176–78. http://dx.doi.org/10.1107/s0108270190001445.
Texto completo da fonteZharkikh, L. N., G. F. Muzychenko, V. G. Kul'nevich, V. E. Zavodnik, K. S. Pushkareva, G. V. Golovko e A. V. Ignatenko. "Reduction of 2-oxa-3,7-diazabicyclo[3.3.0]octanes". Chemistry of Heterocyclic Compounds 28, n.º 7 (julho de 1992): 738–41. http://dx.doi.org/10.1007/bf00474484.
Texto completo da fonteHodgson, David M., e Iain D. Cameron. "Functionalized Bicyclo[3.3.0]octanes by Enantioselective Transannular Desymmetrization". Organic Letters 3, n.º 3 (fevereiro de 2001): 441–44. http://dx.doi.org/10.1021/ol006947n.
Texto completo da fonteXIANG, Y., R. F. SCHINAZI e K. ZHAO. "ChemInform Abstract: Synthesis of (3.3.0) Bicyclic Isoxazolidinyl Nucleosides." ChemInform 27, n.º 47 (4 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199647233.
Texto completo da fonteLee, Jae Wook, Ho Jung Son, Yeon Eui Jung e Jae Ho Lee. "Synthesis of 2,7-Diazabicyclo[3.3.0]octane and 2,7-Diazabicyclo[3.3.0]oct-4-ene Derivatives via Cyclization Reaction and Julia Reaction". Synthetic Communications 26, n.º 8 (abril de 1996): 1499–505. http://dx.doi.org/10.1080/00397919608003516.
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