Статті в журналах з теми "Mycalamide"
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Gürel, Güliz, Gregor Blaha, Thomas A. Steitz, and Peter B. Moore. "Structures of Triacetyloleandomycin and Mycalamide A Bind to the Large Ribosomal Subunit of Haloarcula marismortui." Antimicrobial Agents and Chemotherapy 53, no. 12 (September 8, 2009): 5010–14. http://dx.doi.org/10.1128/aac.00817-09.
Повний текст джерелаRoush, William R., and Lance A. Pfeifer. "Total Synthesis of Mycalamide A and 7-epi-Mycalamide A." Organic Letters 2, no. 6 (March 2000): 859–62. http://dx.doi.org/10.1021/ol005629l.
Повний текст джерелаNakata, Tadashi, Shunya Takahashi, and Akihiro Okada. "Synthesis of Mycalamide Analogs." HETEROCYCLES 63, no. 9 (2004): 2111. http://dx.doi.org/10.3987/com-04-10162.
Повний текст джерелаToyota, M., N. Kagawa, and M. Ihara. "Synthesis of (+)-Mycalamide A." Synfacts 2006, no. 8 (August 2006): 0750. http://dx.doi.org/10.1055/s-2006-941928.
Повний текст джерелаKocienski, Philip J., Robert Narquizian, Piotr Raubo, Christopher Smith, and F. Thomas Boyle. "A Synthesis of Mycalamide B." Synlett 1998, no. 8 (August 1998): 869–72. http://dx.doi.org/10.1055/s-1998-1803.
Повний текст джерелаSohn, Jeong-Hun, Nobuaki Waizumi, H. Marlon Zhong, and Viresh H. Rawal. "Total Synthesis of Mycalamide A." Journal of the American Chemical Society 127, no. 20 (May 2005): 7290–91. http://dx.doi.org/10.1021/ja050728l.
Повний текст джерелаKagawa, Natsuko, Masataka Ihara, and Masahiro Toyota. "Total Synthesis of (+)-Mycalamide A." Organic Letters 8, no. 5 (March 2006): 875–78. http://dx.doi.org/10.1021/ol052943c.
Повний текст джерелаRoush, William R., and Lance A. Pfeifer. "ChemInform Abstract: Total Synthesis of Mycalamide A (IX) and 7-epi-Mycalamide A (V)." ChemInform 31, no. 27 (June 7, 2010): no. http://dx.doi.org/10.1002/chin.200027232.
Повний текст джерелаTrost, Barry M., Hanbiao Yang, and Gary D. Probst. "A Formal Synthesis of (−)-Mycalamide A." Journal of the American Chemical Society 126, no. 1 (January 2004): 48–49. http://dx.doi.org/10.1021/ja038787r.
Повний текст джерелаKagawa, Natsuko, Masataka Ihara, and Masahiro Toyota. "Convergent Total Synthesis of (+)-Mycalamide A." Journal of Organic Chemistry 71, no. 18 (September 2006): 6796–805. http://dx.doi.org/10.1021/jo060803q.
Повний текст джерелаKOCIENSKI, P. J., R. NARQUIZIAN, P. RAUBO, C. SMITH, and F. T. BOYLE. "ChemInform Abstract: A Synthesis of Mycalamide B." ChemInform 29, no. 47 (June 18, 2010): no. http://dx.doi.org/10.1002/chin.199847279.
Повний текст джерелаFUKUI, H., H. MATSUKURA, and T. NAKATA. "ChemInform Abstract: Total Synthesis of Mycalamide A." ChemInform 29, no. 7 (June 24, 2010): no. http://dx.doi.org/10.1002/chin.199807293.
Повний текст джерелаKocienski, Philip, Piotr Raubo, Justin K. Davis, F. Thomas Boyle, Donna E. Davies, and Audrey Richter. "A synthesis of 18-O-methyl mycalamide B." Journal of the Chemical Society, Perkin Transactions 1, no. 15 (1996): 1797. http://dx.doi.org/10.1039/p19960001797.
Повний текст джерелаHoffmann, Reinhard W., and Achim Schlapbach. "Synthesis of the trioxadecalin-part of mycalamide B." Tetrahedron Letters 34, no. 49 (December 1993): 7903–6. http://dx.doi.org/10.1016/s0040-4039(00)61506-x.
Повний текст джерелаKocienski, Philip J. "A Formal Synthesis of 18-O-Methyl Mycalamide B." Synthesis 1999, no. 12 (December 1999): 2087–95. http://dx.doi.org/10.1055/s-1999-3633.
Повний текст джерелаNakata, Tadashi, Shunya Takahashi, Akihiro Okada, and Miho Nishiwaki. "Synthesis and Biological Activities of Sugar Analogs of Mycalamide A." HETEROCYCLES 69, no. 1 (2006): 487. http://dx.doi.org/10.3987/com-06-s(o)35.
Повний текст джерелаFukui, Hideto, Yoshinori Tsuchiya, Keiko Fujita, Tadakiyo Nakagawa, Hiroyuki Koshino, and Tadashi Nakata. "Synthesis and biological activity of artificial analogs of mycalamide A." Bioorganic & Medicinal Chemistry Letters 7, no. 16 (August 1997): 2081–86. http://dx.doi.org/10.1016/s0960-894x(97)00365-x.
Повний текст джерелаHOFFMANN, R. W., and A. SCHLAPBACH. "ChemInform Abstract: Synthesis of the Trioxadecalin Part of Mycalamide B." ChemInform 25, no. 14 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199414299.
Повний текст джерелаKOCIENSKI, P., P. RAUBO, J. K. DAVIS, F. T. BOYLE, D. E. DAVIES, and A. RICHTER. "ChemInform Abstract: A Synthesis of 18-O-Methyl Mycalamide B." ChemInform 28, no. 10 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199710186.
Повний текст джерелаThompson, Andrew M., John W. Blunt, Murray H. G. Munro, and Bruce M. Clark. "Chemistry of the mycalamides, antiviral and antitumour compounds from a marine sponge. Part 4. Reactions of mycalamide A and alkyl derivatives with basic nucleophiles." Journal of the Chemical Society, Perkin Transactions 1, no. 8 (1994): 1025. http://dx.doi.org/10.1039/p19940001025.
Повний текст джерелаNakata, Tadashi, Hideto Fukui, Tadakiyo Nakagawa, and Hiroko Matsukura. "Total Synthesis of Mycalamide A. Further Synthetic Study of the Right Half." HETEROCYCLES 42, no. 1 (1996): 159. http://dx.doi.org/10.3987/com-95-s64.
Повний текст джерелаDang, Y., T. Schneider-Poetsch, D. E. Eyler, J. C. Jewett, S. Bhat, V. H. Rawal, R. Green, and J. O. Liu. "Inhibition of eukaryotic translation elongation by the antitumor natural product Mycalamide B." RNA 17, no. 8 (June 21, 2011): 1578–88. http://dx.doi.org/10.1261/rna.2624511.
Повний текст джерелаNakata, Tadashi, Hiroko Matsukura, Dunlong Jian, and Hiroaki Nagashima. "Synthesis of the right half of mycalamide A. A formal total synthesis." Tetrahedron Letters 35, no. 44 (October 1994): 8229–32. http://dx.doi.org/10.1016/0040-4039(94)88289-4.
Повний текст джерелаWest, Lyndon M., Peter T. Northcote, Kylie A. Hood, John H. Miller, and Michael J. Page. "Mycalamide D, a New Cytotoxic Amide from the New Zealand Marine SpongeMycaleSpecies." Journal of Natural Products 63, no. 5 (May 2000): 707–9. http://dx.doi.org/10.1021/np9904511.
Повний текст джерелаFUKUI, H., Y. TSUCHIYA, K. FUJITA, T. NAKAGAWA, H. KOSHINO, and T. NAKATA. "ChemInform Abstract: Synthesis and Biological Activity of Artificial Analogues of Mycalamide A." ChemInform 28, no. 51 (August 2, 2010): no. http://dx.doi.org/10.1002/chin.199751279.
Повний текст джерелаMarron, Thomas G., and William R. Roush. "Diastereoselective synthesis of N-benzoyl mycalamine, the fully elaborated trioxadecalin nucleus of mycalamide. A. Control of the key N-acyl aminal stereocenter via carbamate acylation." Tetrahedron Letters 36, no. 10 (March 1995): 1581–84. http://dx.doi.org/10.1016/0040-4039(95)00093-r.
Повний текст джерелаTHOMPSON, A. M., J. W. BLUNT, M. H. G. MUNRO, and B. M. CLARK. "ChemInform Abstract: Chemistry of the Mycalamides, Antiviral and Antitumour Compounds from a Marine Sponge. Part 4. Reactions of Mycalamide A and Alkyl Derivatives with Basic Nucleophiles." ChemInform 25, no. 33 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199433295.
Повний текст джерелаIhara, Masataka, Marcellino Rudyanto, Masahiro Toyota, and Natsuko Kagawa. "A Concise Synthesis of a Potential Key Intermediate for 12-epi- Mycalamide A." HETEROCYCLES 58, no. 1 (2002): 655. http://dx.doi.org/10.3987/com-02-s(m)55.
Повний текст джерелаMARRON, T. G., and W. R. ROUSH. "ChemInform Abstract: Diastereoselective Synthesis of N-Benzoyl Mycalamine, the Fully Elaborated Trioxadecalin Nucleus of Mycalamide A. Control of the Key N- Acyl Aminal Stereocenter via Carbamate Acylation." ChemInform 26, no. 38 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199538303.
Повний текст джерелаPerry, Nigel B., John W. Blunt, Murray H. G. Munro, and Lewis K. Pannell. "Mycalamide A, an antiviral compound from a New Zealand sponge of the genus Mycale." Journal of the American Chemical Society 110, no. 14 (July 1988): 4850–51. http://dx.doi.org/10.1021/ja00222a067.
Повний текст джерелаNAKATA, T., H. FUKUI, T. NAKAGAWA, and H. MATSUKURA. "ChemInform Abstract: Total Synthesis of Mycalamide A. Further Synthetic Study of the Right Half." ChemInform 27, no. 17 (August 5, 2010): no. http://dx.doi.org/10.1002/chin.199617241.
Повний текст джерелаNAKATA, T., H. MATSUKURA, D. JIAN, and H. NAGASHIMA. "ChemInform Abstract: Synthesis of the Right Half of Mycalamide A. A Formal Total Synthesis." ChemInform 26, no. 14 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199514250.
Повний текст джерелаMosey, R. Adam, and Paul E. Floreancig. "Isolation, biological activity, synthesis, and medicinal chemistry of the pederin/mycalamide family of natural products." Natural Product Reports 29, no. 9 (2012): 980. http://dx.doi.org/10.1039/c2np20052j.
Повний текст джерелаJewett, John C., and Viresh H. Rawal. "Temporary Restraints To Overcome Steric Obstacles: An Efficient Strategy for the Synthesis of Mycalamide B." Angewandte Chemie International Edition 49, no. 46 (October 7, 2010): 8682–85. http://dx.doi.org/10.1002/anie.201003361.
Повний текст джерелаJewett, John C., and Viresh H. Rawal. "Temporary Restraints To Overcome Steric Obstacles: An Efficient Strategy for the Synthesis of Mycalamide B." Angewandte Chemie 122, no. 46 (October 7, 2010): 8864–67. http://dx.doi.org/10.1002/ange.201003361.
Повний текст джерелаDyshlovoy, Sergey A., Sergey N. Fedorov, Anatoly I. Kalinovsky, Larisa K. Shubina, Carsten Bokemeyer, Valentin A. Stonik, and Friedemann Honecker. "Mycalamide A Shows Cytotoxic Properties and Prevents EGF-Induced Neoplastic Transformation through Inhibition of Nuclear Factors." Marine Drugs 10, no. 12 (May 30, 2012): 1212–24. http://dx.doi.org/10.3390/md10061212.
Повний текст джерелаJiang, Xin, Noelle Williams, and Jef K. De Brabander. "Synthesis of Psymberin Analogues: Probing a Functional Correlation with the Pederin/Mycalamide Family of Natural Products." Organic Letters 9, no. 2 (January 2007): 227–30. http://dx.doi.org/10.1021/ol062656o.
Повний текст джерелаRust, Michael, Eric J. N. Helfrich, Michael F. Freeman, Pakjira Nanudorn, Christopher M. Field, Christian Rückert, Tomas Kündig, et al. "A multiproducer microbiome generates chemical diversity in the marine sponge Mycale hentscheli." Proceedings of the National Academy of Sciences 117, no. 17 (April 14, 2020): 9508–18. http://dx.doi.org/10.1073/pnas.1919245117.
Повний текст джерелаKocienski, Philip, Robert Narquizian, Piotr Raubo, Christopher Smith, Louis J. Farrugia, Kenneth Muir, and F. Thomas Boyle. "Synthetic studies on the pederin family of antitumour agents. Syntheses of mycalamide B, theopederin D and pederin." Journal of the Chemical Society, Perkin Transactions 1, no. 15 (2000): 2357–84. http://dx.doi.org/10.1039/a909898d.
Повний текст джерелаJewett, John C., and Viresh H. Rawal. "ChemInform Abstract: Temporary Restraints to Overcome Steric Obstacles: An Efficient Strategy for the Synthesis of Mycalamide B." ChemInform 42, no. 10 (February 10, 2011): no. http://dx.doi.org/10.1002/chin.201110214.
Повний текст джерелаDAVIS, J., P. J. KOCIENSKI, and T. BOYLE. "ChemInform Abstract: An Approach to the Synthesis of Mycalamide B. Construction of the 2,4, 7-Trioxabicyclo(4.4.0)decane Ring System (XV)." ChemInform 26, no. 16 (April 18, 1995): no. http://dx.doi.org/10.1002/chin.199516301.
Повний текст джерелаKocienski, Philip, Robert Narquizian, Piotr Raubo, Christopher Smith, Louis J. Farrugia, Kenneth Muir, and F. Thomas Boyle. "ChemInform Abstract: Synthetic Studies on the Pederin Family of Antitumor Agents. Syntheses of Mycalamide B (XIII), Theopederin D (XVI) and Pederin (XVIII)." ChemInform 31, no. 48 (November 28, 2000): no. http://dx.doi.org/10.1002/chin.200048240.
Повний текст джерелаGalvin, Frances, Gordon J. Freeman, Ziba Razi-Wolf, Baruj Benacerraf, Lee Nadler, and Hans Reiser. "Effects of cyclosporin A, FK 506, and mycalamide A on the activation of murine CD4+ T cells by the murine B7 antigen." European Journal of Immunology 23, no. 1 (January 1993): 283–86. http://dx.doi.org/10.1002/eji.1830230145.
Повний текст джерелаHong, Chang Yong, and Yoshito Kishi. "Total synthesis of mycalamides A and B." Journal of Organic Chemistry 55, no. 14 (July 1990): 4242–45. http://dx.doi.org/10.1021/jo00301a007.
Повний текст джерелаSimpson, Jamie S., Mary J. Garson, John W. Blunt, Murray H. G. Munro, and John N. A. Hooper. "Mycalamides C and D, Cytotoxic Compounds from the Marine SpongeStylinosn. Species." Journal of Natural Products 63, no. 5 (May 2000): 704–6. http://dx.doi.org/10.1021/np990431z.
Повний текст джерелаZhong, H. Marlon, Jeong-Hun Sohn, and Viresh H. Rawal. "Studies toward the Asymmetric Synthesis of the Right Part of the Mycalamides." Journal of Organic Chemistry 72, no. 2 (January 2007): 386–97. http://dx.doi.org/10.1021/jo0615145.
Повний текст джерелаTrotter, Nicholas S., Shunya Takahashi, and Tadashi Nakata. "Simple and Efficient Synthesis of (+)-Methyl 7-Benzoylpederate, a Key Intermediate toward the Mycalamides." Organic Letters 1, no. 6 (September 1999): 957–59. http://dx.doi.org/10.1021/ol990936g.
Повний текст джерелаGardiner, John M., Richard Mills, and Thomas Fessard. "Synthesis of model ring systems related to C10–C18 analogues of the mycalamides/theopederins." Tetrahedron Letters 45, no. 6 (February 2004): 1215–17. http://dx.doi.org/10.1016/j.tetlet.2003.11.141.
Повний текст джерелаJ. Witczak, Zbigniew, Ricky M. Rampulla, and Ajay Bommareddy. "Mycalamides, Pederin and Psymberin as Natural Carbohydrates and Potential Antitumor Agents: Past and Future Perspectives." Mini-Reviews in Medicinal Chemistry 12, no. 14 (November 1, 2012): 1520–32. http://dx.doi.org/10.2174/138955712803832744.
Повний текст джерелаHoffmann, Reinhard W., Steffen Breitfelder, and Achim Schlapbach. "Model Studies Towards a Novel Fragment Coupling for the Synthesis of Mycalamides and Related Natural Products." Helvetica Chimica Acta 79, no. 2 (March 20, 1996): 346–52. http://dx.doi.org/10.1002/hlca.19960790203.
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