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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. 10 (20 luglio 2015): 2070–83. http://dx.doi.org/10.1002/asia.201500288.
Peng, 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. 46 (27 ottobre 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 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. 00 (2023): 2. http://dx.doi.org/10.2298/jsc221130002k.
Ariztia, 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 (settembre 2021): 116313. http://dx.doi.org/10.1016/j.bmc.2021.116313.
Rios, 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. 5 (2 aprile 2020): 1424–31. http://dx.doi.org/10.1021/acs.jnatprod.9b00759.
Swain, Nigel A., Richard C. D. Brown e Gordon Bruton. "An efficient synthesis of endo,exo-furofuranone derivatives". Chemical Communications, n. 18 (13 agosto 2002): 2042–43. http://dx.doi.org/10.1039/b206150c.
Marchand, 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. 6 (1 giugno 1997): 840–49. http://dx.doi.org/10.1139/v97-102.
Zhang, 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. 17 (2021): 9430–42. http://dx.doi.org/10.1039/d0cs01471k.
Yates, 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. 1 (1 gennaio 1987): 69–77. http://dx.doi.org/10.1139/v87-012.
Yates, Peter, Rupinder S. Grewal, Peter C. Hayes e Jeffery F. Sawyer. "Synthesis of cedranoid sesquiterpenes. V. The biotols". Canadian Journal of Chemistry 66, n. 11 (1 novembre 1988): 2805–15. http://dx.doi.org/10.1139/v88-434.
Delamere, C., C. Jakins e E. Lewars. "Tests for aromaticity applied to the pentalenoquinones A computational study". Canadian Journal of Chemistry 79, n. 10 (1 ottobre 2001): 1492–504. http://dx.doi.org/10.1139/v01-164.
Guthrie, J. Peter, Roger T. Gallant e Michael C. Jennings. "Preparation and characterization of bicyclic amide acetals and monothioacetals". Canadian Journal of Chemistry 82, n. 2 (1 febbraio 2004): 268–78. http://dx.doi.org/10.1139/v03-204.
Riaz, 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. 12 (1 dicembre 2000): 1216–20. http://dx.doi.org/10.1515/znb-2000-1217.
Yu, Zhi-Xiang, e Cheng-Hang Liu. "Rh(I)-Catalyzed Intramolecular [3+2] Cycloaddition of trans-2-Allene-Vinylcyclopropanes". Synlett 29, n. 06 (18 gennaio 2018): 764–68. http://dx.doi.org/10.1055/s-0037-1609199.
Tănase, 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. 46 (2020): 20405–10. http://dx.doi.org/10.1039/d0nj04594b.
Robertson, Jeremy, e Kiri Stevens. "Pyrrolizidine alkaloids". Nat. Prod. Rep. 31, n. 12 (2014): 1721–88. http://dx.doi.org/10.1039/c4np00055b.
Deslongchamps, 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. 4 (1 aprile 1994): 1162–64. http://dx.doi.org/10.1139/v94-148.
Krech, Friedrich, Babett Krauss, Adolf Zschunke e Clemens Mügge. "Cis-1-phosphabicyclo[3.3.0]octan". Zeitschrift für anorganische und allgemeine Chemie 629, n. 9 (agosto 2003): 1475–76. http://dx.doi.org/10.1002/zaac.200300096.
Gimazetdinov, 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. 14 (2022): 6708–14. http://dx.doi.org/10.1039/d2nj01003h.
Robertson, Jeremy, e Kiri Stevens. "Pyrrolizidine alkaloids: occurrence, biology, and chemical synthesis". Natural Product Reports 34, n. 1 (2017): 62–89. http://dx.doi.org/10.1039/c5np00076a.
Antoniadis, 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. 7 (1 luglio 1987): 1557–62. http://dx.doi.org/10.1139/v87-262.
Aurich, 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. 1 (1 gennaio 1999): 87–95. http://dx.doi.org/10.1515/znb-1999-0117.
Brandstätter, 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. 35 (2019): 8219–23. http://dx.doi.org/10.1039/c9sc02828e.
Bhat, 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. 11 (13 ottobre 2020): 1726–53. http://dx.doi.org/10.1002/ajoc.202000401.
Flippen-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. 9 (23 agosto 2002): o1018—o1020. http://dx.doi.org/10.1107/s1600536802014101.
Baumeister, U., H. Hartung e F. Krech. "1-Phosphabicyclo[3.3.0]octane 1-sulfide". Acta Crystallographica Section C Crystal Structure Communications 46, n. 4 (15 aprile 1990): 634–37. http://dx.doi.org/10.1107/s0108270189008085.
Eberle, 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. 5 (30 aprile 2001): o461—o462. http://dx.doi.org/10.1107/s1600536801006808.
Ma, Chenxi, e Anthony F. Hill. "Methimazolyl based diptych bicyclo-[3.3.0]-ruthenaboratranes". Dalton Transactions 48, n. 6 (2019): 1976–92. http://dx.doi.org/10.1039/c8dt04813d.
Xiang, Yuejun, Raymond F. Schinazi e Kang Zhao. "Synthesis of [3.3.0] bicyclic isoxazolidinyl nucleosides". Bioorganic & Medicinal Chemistry Letters 6, n. 13 (luglio 1996): 1475–78. http://dx.doi.org/10.1016/s0960-894x(96)00262-4.
Vega, 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. 4 (8 marzo 2008): o199—o204. http://dx.doi.org/10.1107/s0108270108004290.
Knotnerus, 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. 11 (2 settembre 2010): 1185–90. http://dx.doi.org/10.1002/recl.19640831110.
Muhit, 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 (settembre 2016): 74–79. http://dx.doi.org/10.1016/j.fitote.2016.07.004.
Gund, Machhindra, Martin Déry e Claude Spino. "Synthesis of carotol using a formal (4+1)-cycloaddition of chiral dialkoxycarbenes". Canadian Journal of Chemistry 96, n. 3 (marzo 2018): 311–27. http://dx.doi.org/10.1139/cjc-2017-0594.
Grygorenko, 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. 14 (13 aprile 2017): 3112–17. http://dx.doi.org/10.1055/s-0036-1588785.
Tanase, 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. 2 (7 maggio 2021): 156–77. http://dx.doi.org/10.37358/rc.21.2.8428.
Quast, 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. 5 (19 maggio 1992): 495–511. http://dx.doi.org/10.1002/jlac.199219920188.
Becheanu, 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. 5 (1 maggio 2006): 589–96. http://dx.doi.org/10.1515/znb-2006-0514.
Kliegel, 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. 7 (1 luglio 1992): 2022–26. http://dx.doi.org/10.1139/v92-254.
Bird, C. W., E. C. J. Coffee e B. W. C. Schmidl. "Bicyclo [3.3.0]Octane Derivatives for Carbaprostacyclin Synthesis". Synthetic Communications 23, n. 5 (1 marzo 1993): 613–20. http://dx.doi.org/10.1080/00397919308009819.
Lachaise, I., K. Nohair, M. Hakiki e J. Y. Nédélec. "A Straightforward Synthesis of [3.3.0]Bicyclic Compounds". Synthetic Communications 25, n. 22 (novembre 1995): 3529–36. http://dx.doi.org/10.1080/00397919508015487.
Archibald, T. G., e K. Baum. "Synthesis of Polynitro-2,6-dioxabicyclo[3.3.0]octanes". Synthetic Communications 19, n. 9-10 (giugno 1989): 1493–98. http://dx.doi.org/10.1080/00397918908051042.
Tanaka, 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. 9 (settembre 2003): 535–37. http://dx.doi.org/10.3184/030823403322597207.
Bartmann, 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. 1 (1989): 189–95. http://dx.doi.org/10.1135/cccc19890189.
Stachel, 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. 3 (1997): 510–15. http://dx.doi.org/10.1135/cccc19970510.
Butcher, 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. 9 (21 agosto 2004): o1543—o1545. http://dx.doi.org/10.1107/s160053680401880x.
Cronan 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. 6 (15 giugno 1990): 1176–78. http://dx.doi.org/10.1107/s0108270190001445.
Zharkikh, 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. 7 (luglio 1992): 738–41. http://dx.doi.org/10.1007/bf00474484.
Hodgson, David M., e Iain D. Cameron. "Functionalized Bicyclo[3.3.0]octanes by Enantioselective Transannular Desymmetrization". Organic Letters 3, n. 3 (febbraio 2001): 441–44. http://dx.doi.org/10.1021/ol006947n.
XIANG, Y., R. F. SCHINAZI e K. ZHAO. "ChemInform Abstract: Synthesis of (3.3.0) Bicyclic Isoxazolidinyl Nucleosides." ChemInform 27, n. 47 (4 agosto 2010): no. http://dx.doi.org/10.1002/chin.199647233.
Lee, 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. 8 (aprile 1996): 1499–505. http://dx.doi.org/10.1080/00397919608003516.