Статті в журналах з теми "[3.3.0]furofuranone"
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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.
Delamere, C., C. Jakins, and E. Lewars. "Tests for aromaticity applied to the pentalenoquinones A computational study." Canadian Journal of Chemistry 79, no. 10 (October 1, 2001): 1492–504. http://dx.doi.org/10.1139/v01-164.
Guthrie, J. Peter, Roger T. Gallant, and Michael C. Jennings. "Preparation and characterization of bicyclic amide acetals and monothioacetals." Canadian Journal of Chemistry 82, no. 2 (February 1, 2004): 268–78. http://dx.doi.org/10.1139/v03-204.
Riaz, Muhammad, Nisar Ullah, Arshad Mehmood, Hafiz Rab Nawaz, Abdul Malik, and Nighat Afza. "Furanoid and Furofuranoid Lignans from Daphne oleoides." Zeitschrift für Naturforschung B 55, no. 12 (December 1, 2000): 1216–20. http://dx.doi.org/10.1515/znb-2000-1217.
Yu, Zhi-Xiang, and Cheng-Hang Liu. "Rh(I)-Catalyzed Intramolecular [3+2] Cycloaddition of trans-2-Allene-Vinylcyclopropanes." Synlett 29, no. 06 (January 18, 2018): 764–68. http://dx.doi.org/10.1055/s-0037-1609199.
Tănase, Constantin I., Constantin Drăghici та 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, № 46 (2020): 20405–10. http://dx.doi.org/10.1039/d0nj04594b.
Robertson, Jeremy, and Kiri Stevens. "Pyrrolizidine alkaloids." Nat. Prod. Rep. 31, no. 12 (2014): 1721–88. http://dx.doi.org/10.1039/c4np00055b.
Deslongchamps, Ghislain, Daniel Mink, Paul D. Boyle, and Nina Singh. "Unusual Weiss–Cook condensation of dimethyl 2,3-dioxobutanedioate and dimethyl 3-oxoglutarate." Canadian Journal of Chemistry 72, no. 4 (April 1, 1994): 1162–64. http://dx.doi.org/10.1139/v94-148.
Krech, Friedrich, Babett Krauss, Adolf Zschunke, and Clemens Mügge. "Cis-1-phosphabicyclo[3.3.0]octan." Zeitschrift für anorganische und allgemeine Chemie 629, no. 9 (August 2003): 1475–76. http://dx.doi.org/10.1002/zaac.200300096.
Gimazetdinov, Airat M., Aidar Z. Al’mukhametov та 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, № 14 (2022): 6708–14. http://dx.doi.org/10.1039/d2nj01003h.
Robertson, Jeremy, and Kiri Stevens. "Pyrrolizidine alkaloids: occurrence, biology, and chemical synthesis." Natural Product Reports 34, no. 1 (2017): 62–89. http://dx.doi.org/10.1039/c5np00076a.
Antoniadis, Greg A., Michael T. M. Clements, Sriyawathie Peiris та 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, № 7 (1 липня 1987): 1557–62. http://dx.doi.org/10.1139/v87-262.
Aurich, Hans Günter, and 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, no. 1 (January 1, 1999): 87–95. http://dx.doi.org/10.1515/znb-1999-0117.
Brandstätter, Marco, Nikolas Huwyler, and 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, no. 35 (2019): 8219–23. http://dx.doi.org/10.1039/c9sc02828e.
Bhat, Bilal A., Showkat Rashid, and Goverdhan Mehta. "Progress in the Total Synthesis of Natural Products Embodying Diverse Furofuranone Motifs: A New Millennium Update." Asian Journal of Organic Chemistry 9, no. 11 (October 13, 2020): 1726–53. http://dx.doi.org/10.1002/ajoc.202000401.
Flippen-Anderson, Judith L., Jeffrey R. Deschamps, Clifford George, and Richard D. Gilardi. "4,4,8,8-Tetranitro-2,6-dioxabicyclo[3.3.0]octane." Acta Crystallographica Section E Structure Reports Online 58, no. 9 (August 23, 2002): o1018—o1020. http://dx.doi.org/10.1107/s1600536802014101.
Baumeister, U., H. Hartung, and F. Krech. "1-Phosphabicyclo[3.3.0]octane 1-sulfide." Acta Crystallographica Section C Crystal Structure Communications 46, no. 4 (April 15, 1990): 634–37. http://dx.doi.org/10.1107/s0108270189008085.
Eberle, Marcel K., Reinhart Keese, and Helen Stoeckli-Evans. "A bicyclo[3.3.0]octan-2-ylcyclopentanone." Acta Crystallographica Section E Structure Reports Online 57, no. 5 (April 30, 2001): o461—o462. http://dx.doi.org/10.1107/s1600536801006808.
Ma, Chenxi, and Anthony F. Hill. "Methimazolyl based diptych bicyclo-[3.3.0]-ruthenaboratranes." Dalton Transactions 48, no. 6 (2019): 1976–92. http://dx.doi.org/10.1039/c8dt04813d.
Xiang, Yuejun, Raymond F. Schinazi, and Kang Zhao. "Synthesis of [3.3.0] bicyclic isoxazolidinyl nucleosides." Bioorganic & Medicinal Chemistry Letters 6, no. 13 (July 1996): 1475–78. http://dx.doi.org/10.1016/s0960-894x(96)00262-4.
Vega, Andrés, Oscar Donoso-Tauda, Andres Ibañez, and Carlos A. Escobar. "Five bicyclo[3.3.0]octa-2,6-dienes." Acta Crystallographica Section C Crystal Structure Communications 64, no. 4 (March 8, 2008): o199—o204. http://dx.doi.org/10.1107/s0108270108004290.
Knotnerus, J., and 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, no. 11 (September 2, 2010): 1185–90. http://dx.doi.org/10.1002/recl.19640831110.
Muhit, Md Abdul, Kaoru Umehara, and Hiroshi Noguchi. "Five furofuranone lignan glucosides from Terminalia citrina inhibit in vitro E 2 -enhanced breast cancer cell proliferation." Fitoterapia 113 (September 2016): 74–79. http://dx.doi.org/10.1016/j.fitote.2016.07.004.
Gund, Machhindra, Martin Déry, and Claude Spino. "Synthesis of carotol using a formal (4+1)-cycloaddition of chiral dialkoxycarbenes." Canadian Journal of Chemistry 96, no. 3 (March 2018): 311–27. http://dx.doi.org/10.1139/cjc-2017-0594.
Grygorenko, Oleksandr, Yevhenii Sokolenko, Eugeniy Ostapchuk, and Artem Artemenko. "An Approach to 3-Oxa-7-azabicyclo[3.3.0]octanes – Bicyclic Morpholine Surrogates." Synthesis 49, no. 14 (April 13, 2017): 3112–17. http://dx.doi.org/10.1055/s-0036-1588785.
Tanase, Constantin I., Anamaria Hanganu, and 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, no. 2 (May 7, 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, and 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, no. 5 (May 19, 1992): 495–511. http://dx.doi.org/10.1002/jlac.199219920188.
Becheanu, Armand, Thomas Bell, Sabine Laschat, Angelika Baro, Wolfgang Frey, Nelli Steinke, and Peter Fischer. "Synthesis of Pentalene Systems Employing a Sequence of Pauson-Khand Reaction, Michael Reaction, and Desilylation." Zeitschrift für Naturforschung B 61, no. 5 (May 1, 2006): 589–96. http://dx.doi.org/10.1515/znb-2006-0514.
Kliegel, Wolfgang, Gottfried Lubkowitz, Steven J. Rettig, and 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, no. 7 (July 1, 1992): 2022–26. http://dx.doi.org/10.1139/v92-254.
Bird, C. W., E. C. J. Coffee, and B. W. C. Schmidl. "Bicyclo [3.3.0]Octane Derivatives for Carbaprostacyclin Synthesis." Synthetic Communications 23, no. 5 (March 1, 1993): 613–20. http://dx.doi.org/10.1080/00397919308009819.
Lachaise, I., K. Nohair, M. Hakiki, and J. Y. Nédélec. "A Straightforward Synthesis of [3.3.0]Bicyclic Compounds." Synthetic Communications 25, no. 22 (November 1995): 3529–36. http://dx.doi.org/10.1080/00397919508015487.
Archibald, T. G., and K. Baum. "Synthesis of Polynitro-2,6-dioxabicyclo[3.3.0]octanes." Synthetic Communications 19, no. 9-10 (June 1989): 1493–98. http://dx.doi.org/10.1080/00397918908051042.
Tanaka, Koichi, Tomoyuki Watanabe, and 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, no. 9 (September 2003): 535–37. http://dx.doi.org/10.3184/030823403322597207.
Bartmann, Wilhelm, Gerhard Beck, Wolfram Fehlhaber, and 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, no. 1 (1989): 189–95. http://dx.doi.org/10.1135/cccc19890189.
Stachel, Hans-Dietrich, Želmíra Odlerová, and Karel Waisser. "A New Pharmacophore of Potential Antimycobacterial Activity: The Disulfide Group in the Ring of Alicyclic Compounds." Collection of Czechoslovak Chemical Communications 62, no. 3 (1997): 510–15. http://dx.doi.org/10.1135/cccc19970510.
Butcher, Ray J., Robin Evans, and 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, no. 9 (August 21, 2004): o1543—o1545. http://dx.doi.org/10.1107/s160053680401880x.
Cronan Jnr, J. M., F. R. Fronczek, and M. L. McLaughlin. "A bichromophoric difulvene from 3,7-bicyclo[3.3.0]octadione." Acta Crystallographica Section C Crystal Structure Communications 46, no. 6 (June 15, 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, and A. V. Ignatenko. "Reduction of 2-oxa-3,7-diazabicyclo[3.3.0]octanes." Chemistry of Heterocyclic Compounds 28, no. 7 (July 1992): 738–41. http://dx.doi.org/10.1007/bf00474484.
Hodgson, David M., and Iain D. Cameron. "Functionalized Bicyclo[3.3.0]octanes by Enantioselective Transannular Desymmetrization." Organic Letters 3, no. 3 (February 2001): 441–44. http://dx.doi.org/10.1021/ol006947n.
XIANG, Y., R. F. SCHINAZI, and K. ZHAO. "ChemInform Abstract: Synthesis of (3.3.0) Bicyclic Isoxazolidinyl Nucleosides." ChemInform 27, no. 47 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199647233.
Lee, Jae Wook, Ho Jung Son, Yeon Eui Jung, and 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, no. 8 (April 1996): 1499–505. http://dx.doi.org/10.1080/00397919608003516.