Статті в журналах з теми "Total Synthesis, Methodology"
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Petrovčič, Jan, Chad Nicholas Ungarean, and David Sarlah. "Recent Chemical Methodology Advances in the Total Synthesis of Meroterpenoids." Acta Chimica Slovenica 68, no. 2 (June 15, 2021): 247–67. http://dx.doi.org/10.17344/acsi.2021.6921.
Повний текст джерелаIsobe, Minoru, and Akinari Hamajima. "Ciguatoxin: developing the methodology for total synthesis." Natural Product Reports 27, no. 8 (2010): 1204. http://dx.doi.org/10.1039/b919467n.
Повний текст джерелаUmezawa, Taiki, and Fuyuhiko Matsuda. "Recent progress toward synthesis of chlorosulfolipids: total synthesis and methodology." Tetrahedron Letters 55, no. 19 (May 2014): 3003–12. http://dx.doi.org/10.1016/j.tetlet.2014.03.082.
Повний текст джерелаWilliams, Craig, and Rebecca Pouwer. "Method in the Madness - Methodology from Total Synthesis." Synlett 23, no. 10 (May 29, 2012): 1446–58. http://dx.doi.org/10.1055/s-0031-1290967.
Повний текст джерелаVedejs, Edwin, and Chutima Kongkittingam. "A Total Synthesis of (−)-Hemiasterlin UsingN-Bts Methodology." Journal of Organic Chemistry 66, no. 22 (November 2001): 7355–64. http://dx.doi.org/10.1021/jo0104882.
Повний текст джерелаKeck, Gary E., Eugene P. Boden, and Michael R. Wiley. "Total synthesis of (+)-colletodiol: new methodology for the synthesis of macrolactones." Journal of Organic Chemistry 54, no. 4 (February 1989): 896–906. http://dx.doi.org/10.1021/jo00265a033.
Повний текст джерелаUmezawa, Taiki, and Fuyuhiko Matsuda. "ChemInform Abstract: Recent Progress Toward Synthesis of Chlorosulfolipids: Total Synthesis and Methodology." ChemInform 45, no. 29 (July 3, 2014): no. http://dx.doi.org/10.1002/chin.201429265.
Повний текст джерелаYeung, Kay, Rory C. Mykura, and Varinder K. Aggarwal. "Lithiation–borylation methodology in the total synthesis of natural products." Nature Synthesis 1, no. 2 (February 2022): 117–26. http://dx.doi.org/10.1038/s44160-021-00012-1.
Повний текст джерелаXiang, Alan X., Donald A. Watson, Taotao Ling, and Emmanuel A. Theodorakis. "Total Synthesis of Clerocidin via a Novel, Enantioselective Homoallenylboration Methodology." Journal of Organic Chemistry 63, no. 20 (October 1998): 6774–75. http://dx.doi.org/10.1021/jo981331l.
Повний текст джерелаJohnstone, Craig, William J. Kerr, and Udo Lange. "Total synthesis of (+)-taylorione utilising modified Pauson–Khand reaction methodology." J. Chem. Soc., Chem. Commun., no. 4 (1995): 457–58. http://dx.doi.org/10.1039/c39950000457.
Повний текст джерелаPouwer, Rebecca H., and Craig M. Williams. "ChemInform Abstract: Method in the Madness - Methodology from Total Synthesis." ChemInform 43, no. 35 (August 2, 2012): no. http://dx.doi.org/10.1002/chin.201235244.
Повний текст джерелаBaati, Rachid, John R. Falck, and Charles Mioskowski. "ChemInform Abstract: Chromium in Organic Synthesis. From Methodology to Total Synthesis of Natural Products." ChemInform 41, no. 1 (January 5, 2010): no. http://dx.doi.org/10.1002/chin.201001248.
Повний текст джерелаVedejs, Edwin, and Chutima Kongkittingam. "ChemInform Abstract: A Total Synthesis of (-)-Hemiasterlin Using N-Bts Methodology." ChemInform 33, no. 15 (May 22, 2010): no. http://dx.doi.org/10.1002/chin.200215196.
Повний текст джерелаEnders, Dieter, Sylvie Dhulut, Daniel Steinbusch, and Audrey Herrbach. "Asymmetric Total Synthesis of (−)-Pironetin Employing the SAMP/RAMP Hydrazone Methodology." Chemistry - A European Journal 13, no. 14 (May 7, 2007): 3942–49. http://dx.doi.org/10.1002/chem.200601672.
Повний текст джерелаNicolaou, K. C., Hui Li, Christopher N. C. Boddy, Joshi M. Ramanjulu, Tai-Yuen Yue, Swaminathan Natarajan, Xin-Jie Chu, Stefan Bräse, and Frank Rübsam. "Total Synthesis of Vancomycin—Part 1: Design and Development of Methodology." Chemistry - A European Journal 5, no. 9 (September 3, 1999): 2584–601. http://dx.doi.org/10.1002/(sici)1521-3765(19990903)5:9<2584::aid-chem2584>3.0.co;2-b.
Повний текст джерелаKatoh, Tadashi. "Enantioselective Total Synthesis of Otteliones A and B, Novel and Powerful Antitumor Agents from the Freshwater Plant Ottelia alismoides." Natural Product Communications 8, no. 7 (July 2013): 1934578X1300800. http://dx.doi.org/10.1177/1934578x1300800724.
Повний текст джерелаFukuyama, Tohru. "Total Synthesis of Nitrogen-Containing Natural Products and Development of Synthetic Methodology." Journal of Synthetic Organic Chemistry, Japan 61, no. 6 (2003): 620–30. http://dx.doi.org/10.5059/yukigoseikyokaishi.61.620.
Повний текст джерелаTarrade, Aurélie, Philippe Dauban та Robert H. Dodd. "Enantiospecific Total Synthesis of (−)-Polyoxamic Acid Using 2,3-Aziridino-γ-lactone Methodology". Journal of Organic Chemistry 68, № 24 (листопад 2003): 9521–24. http://dx.doi.org/10.1021/jo035039b.
Повний текст джерелаWasserman, Harry H., and Rui Zhang. "Total synthesis of cyclotheonamides E2 and E3: application of cyano ylide methodology." Tetrahedron Letters 43, no. 20 (May 2002): 3743–46. http://dx.doi.org/10.1016/s0040-4039(02)00599-3.
Повний текст джерелаFaul, Margaret M., and Bret E. Huff. "Strategy and Methodology Development for the Total Synthesis of Polyether Ionophore Antibiotics†." Chemical Reviews 100, no. 6 (June 2000): 2407–74. http://dx.doi.org/10.1021/cr940210s.
Повний текст джерелаJOHNSTONE, C., W. J. KERR, and U. LANGE. "ChemInform Abstract: Total Synthesis of (+)-Taylorione Utilizing Modified Pauson-Khand Reaction Methodology." ChemInform 26, no. 32 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199532188.
Повний текст джерелаRoche, Stéphane P, Sophie Faure, and David J Aitken. "Total Synthesis of Cyclotheonamide C using a Tandem Backbone-Extension-Coupling Methodology." Angewandte Chemie International Edition 47, no. 36 (August 25, 2008): 6840–42. http://dx.doi.org/10.1002/anie.200802005.
Повний текст джерелаRoche, Stéphane P, Sophie Faure, and David J Aitken. "Total Synthesis of Cyclotheonamide C using a Tandem Backbone-Extension-Coupling Methodology." Angewandte Chemie 120, no. 36 (July 25, 2008): 6946–48. http://dx.doi.org/10.1002/ange.200802005.
Повний текст джерелаXIANG, A. X., D. A. WATSON, T. LING, and E. A. THEODORAKIS. "ChemInform Abstract: Total Synthesis of Clerocidin via a Novel, Enantioselective Homoallenylboration Methodology." ChemInform 30, no. 7 (June 17, 2010): no. http://dx.doi.org/10.1002/chin.199907264.
Повний текст джерелаAnderson, Oren P., Anthony GM Barrett, Jeremy J. Edmunds, Shun-Ichiro Hachiya, James A. Hendrix, Kiyoshi Horita, James W. Malecha, Christopher J. Parkinson, and Andrew VanSickle. "Applications of crotyldiisopinocampheylboranes in synthesis: a formal total synthesis of (+)-calyculin A." Canadian Journal of Chemistry 79, no. 11 (November 1, 2001): 1562–92. http://dx.doi.org/10.1139/v01-133.
Повний текст джерелаElford, Tim G., Stefan Nave, Ravindra P. Sonawane, and Varinder K. Aggarwal. "Total Synthesis of (+)-Erogorgiaene Using Lithiation–Borylation Methodology, and Stereoselective Synthesis of Each of Its Diastereoisomers." Journal of the American Chemical Society 133, no. 42 (October 26, 2011): 16798–801. http://dx.doi.org/10.1021/ja207869f.
Повний текст джерелаMaity, Arindam, Avishek Roy, Mrinal Kanti Das, Subhadip De, Malay Naskar, and Alakesh Bisai. "Oxidative cyanation of 2-oxindoles: formal total synthesis of (±)-gliocladin C." Organic & Biomolecular Chemistry 18, no. 8 (2020): 1679–84. http://dx.doi.org/10.1039/c9ob02752a.
Повний текст джерелаKingsbury, Jason S., та E. J. Corey. "Enantioselective Total Synthesis of Isoedunol and β-Araneosene Featuring Unconventional Strategy and Methodology". Journal of the American Chemical Society 127, № 40 (жовтень 2005): 13813–15. http://dx.doi.org/10.1021/ja055137+.
Повний текст джерелаSrikrishna, A., T. Jagadeeswar Reddy, P. Praveen Kumar, and D. Vijaykumar. "A Methodology for Spirocyclopentannulation. Stereoselective Total Synthesis of (±)-Tochuinyl Acetate and (±)-Dihydrotochuinyl Acetate." Synlett 1996, no. 01 (January 1996): 67–68. http://dx.doi.org/10.1055/s-1996-5318.
Повний текст джерелаVicario, Jose L., Andreas Job, Michael Wolberg, Michael Müller, and Dieter Enders. "Asymmetric Total Synthesis of (−)-Callystatin A Employing the SAMP/RAMP Hydrazone Alkylation Methodology." Organic Letters 4, no. 6 (March 2002): 1023–26. http://dx.doi.org/10.1021/ol0256116.
Повний текст джерелаCampbell, Andrew D., Richard J. K. Taylor та Tony M. Raynham. "The total synthesis of (−)-α-kainic acid using titanium-mediated diene metallabicyclisation methodology". Chemical Communications, № 3 (1999): 245–46. http://dx.doi.org/10.1039/a809598a.
Повний текст джерелаWang, Qian, and Jie-Ping Zhu. "ChemInform Abstract: Total Synthesis of Natural Products and the Synergy with Synthetic Methodology." ChemInform 44, no. 23 (May 16, 2013): no. http://dx.doi.org/10.1002/chin.201323207.
Повний текст джерелаWeinreb, Steven M. "Development of methodology for amide oxidation and its application to total synthesis ofsecurinegaalkaloids." Journal of Heterocyclic Chemistry 33, no. 5 (September 1996): 1437–43. http://dx.doi.org/10.1002/jhet.5570330503.
Повний текст джерелаDubasi, Narsimhaswamy, and Ravi Varala. "Studies towards the Total Synthesis of (+)-Discodermolide: Desymmetrization Approach." Caribbean Journal of Science and Technology 10, no. 01 (2022): 28–35. http://dx.doi.org/10.55434/cbi.2022.10105.
Повний текст джерелаMunda, Mintu, Sovan Niyogi, Kundan Shaw, Sourav Kundu, Rhituparna Nandi, and Alakesh Bisai. "Electrocatalysis as a key strategy for the total synthesis of natural products." Organic & Biomolecular Chemistry 20, no. 4 (2022): 727–48. http://dx.doi.org/10.1039/d1ob02115j.
Повний текст джерелаGueyrard, David. "Extension of the Modified Julia Olefination on Carboxylic Acid Derivatives: Scope and Applications." Synlett 29, no. 01 (October 16, 2017): 34–45. http://dx.doi.org/10.1055/s-0036-1590916.
Повний текст джерелаCorey, E. J., and Michael A. Letavic. "Enantioselective Total Synthesis of Gracilins B and C Using Catalytic Asymmetric Diels-Alder Methodology." Journal of the American Chemical Society 117, no. 37 (September 1995): 9616–17. http://dx.doi.org/10.1021/ja00142a051.
Повний текст джерелаHeathcock, Clayton H., and Stephen H. Montgomery. "Acyclic stereoselection. 28. Use of stereoselective aldol methodology in the total synthesis of cladinose." Tetrahedron Letters 26, no. 8 (January 1985): 1001–4. http://dx.doi.org/10.1016/s0040-4039(00)98496-x.
Повний текст джерелаGareau, Yves, Robert Zamboni, and Alexander W. Wong. "Total synthesis of N-methyl LTC4: a novel methodology for the monomethylation of amines." Journal of Organic Chemistry 58, no. 6 (March 1993): 1582–85. http://dx.doi.org/10.1021/jo00058a049.
Повний текст джерелаFaul, Margaret M., and Bret E. Huff. "ChemInform Abstract: Strategy and Methodology Development for the Total Synthesis of Polyether Ionorephore Antibiotics." ChemInform 31, no. 34 (June 3, 2010): no. http://dx.doi.org/10.1002/chin.200034265.
Повний текст джерелаWasserman, Harry H., and Rui Zhang. "ChemInform Abstract: Total Synthesis of Cyclotheonamides E2 and E3: Application of Cyano Ylide Methodology." ChemInform 33, no. 36 (May 20, 2010): no. http://dx.doi.org/10.1002/chin.200236189.
Повний текст джерелаHashimoto, Hajime, Shinnosuke Wakamori, Kazutada Ikeuchi, and Hidetoshi Yamada. "Divergent Synthesis of Four Monomeric Ellagitannins toward the Total Synthesis of an Oligomeric Ellagitannin, Nobotanin K." Organics 3, no. 3 (September 6, 2022): 293–303. http://dx.doi.org/10.3390/org3030022.
Повний текст джерелаZhu, Bin, and James S. Panek. "Methodology Based on Chiral Silanes in the Synthesis of Polypropionate-Derived Natural Products − Total Synthesis of Epothilone A." European Journal of Organic Chemistry 2001, no. 9 (May 2001): 1701–14. http://dx.doi.org/10.1002/1099-0690(200105)2001:9<1701::aid-ejoc1701>3.0.co;2-#.
Повний текст джерелаRoesner, Stefan, and Varinder K. Aggarwal. "Enantioselective synthesis of (R)-tolterodine using lithiation/borylation–protodeboronation methodology." Canadian Journal of Chemistry 90, no. 11 (November 2012): 965–74. http://dx.doi.org/10.1139/v2012-069.
Повний текст джерелаIsoda, Yuta, Norihiko Sasaki, Kei Kitamura, Shuji Takahashi, Sujit Manmode, Naoko Takeda-Okuda, Jun-ichi Tamura, Toshiki Nokami, and Toshiyuki Itoh. "Total synthesis of TMG-chitotriomycin based on an automated electrochemical assembly of a disaccharide building block." Beilstein Journal of Organic Chemistry 13 (May 16, 2017): 919–24. http://dx.doi.org/10.3762/bjoc.13.93.
Повний текст джерелаLübken, Dennis, Marius Saxarra, and Markus Kalesse. "Tris(acetylacetonato) Iron(III): Recent Developments and Synthetic Applications." Synthesis 51, no. 01 (November 27, 2018): 161–77. http://dx.doi.org/10.1055/s-0037-1610393.
Повний текст джерелаYao, Sulan, Mogens Johannsen, Rita G. Hazell, and Karl Anker Jørgensen. "Total Synthesis of (R)-Dihydroactinidiolide and (R)-Actinidiolide Using Asymmetric Catalytic Hetero-Diels−Alder Methodology." Journal of Organic Chemistry 63, no. 1 (January 1998): 118–21. http://dx.doi.org/10.1021/jo971528y.
Повний текст джерелаSRIKRISHNA, A., T. J. REDDY, P. P. KUMAR, and D. VIJAYKUMAR. "ChemInform Abstract: A Methodology for Spirocyclopentannulation. Stereoselective Total Synthesis of (.+-.)-Tochuinyl Acetate and (.+-.)-Dihydrotochuinyl Acetate." ChemInform 27, no. 19 (August 5, 2010): no. http://dx.doi.org/10.1002/chin.199619094.
Повний текст джерелаCampbell, Andrew D., Tony M. Raynham та Richard J. K. Taylor. "ChemInform Abstract: The Total Synthesis of (-)-α-Kainic Acid Using Titanium-Mediated Diene Metallabicyclization Methodology." ChemInform 30, № 22 (15 червня 2010): no. http://dx.doi.org/10.1002/chin.199922197.
Повний текст джерелаVicario, Jose L., Andreas Job, Michael Wolberg, Michael Mueller, and Dieter Enders. "ChemInform Abstract: Asymmetric Total Synthesis of (-)-Callystatin A Employing the SAMP/RAMP Hydrazone Alkylation Methodology." ChemInform 33, no. 36 (May 20, 2010): no. http://dx.doi.org/10.1002/chin.200236220.
Повний текст джерела