Статті в журналах з теми "Synthesis of Allocolchicine"
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Fedorov, Alexey, Ekaterina Shchegravina, Elena Svirshchevskaya, and Hans-Günther Schmalz. "A Facile Synthetic Approach to Nonracemic Substituted Pyrrolo-allocolchicinoids Starting from Natural Colchicine." Synthesis 51, no. 07 (December 13, 2018): 1611–22. http://dx.doi.org/10.1055/s-0037-1610673.
Повний текст джерелаSitnikov, Nikolay S., Alexander V. Sinzov, Diane Allegro, Pascale Barbier, Sebastien Combes, Liliane Abodo Onambele, Aram Prokop, Hans-Günther Schmalz, and Alexey Yu Fedorov. "Synthesis of indole-derived allocolchicine congeners exhibiting pronounced anti-proliferative and apoptosis-inducing properties." MedChemComm 6, no. 12 (2015): 2158–62. http://dx.doi.org/10.1039/c5md00320b.
Повний текст джерелаDjurdjevic, Sinisa, Fei Yang, and James R. Green. "Intramolecular Nicholas Reactions in the Synthesis of Dibenzocycloheptanes. Synthesis of Allocolchicine NSC 51046 and Analogues and the Formal Synthesis of (−)-Allocolchicine." Journal of Organic Chemistry 75, no. 23 (December 3, 2010): 8241–51. http://dx.doi.org/10.1021/jo101953n.
Повний текст джерелаFedorov, Alexey, Iuliia Gracheva, Elena Svirshchevskaya, Vladimir Faerman, and Irina Beletskaya. "Synthesis and Antiproliferative Properties of Bifunctional Allocolchicine Derivatives." Synthesis 50, no. 14 (May 28, 2018): 2753–60. http://dx.doi.org/10.1055/s-0037-1610146.
Повний текст джерелаZotov, A. S., E. S. Shchegravina, and A. Yu Fedorov. "Synthesis of Allocolchicine Conjugates with a Cetirizine Analog." Russian Journal of Organic Chemistry 54, no. 10 (October 2018): 1498–504. http://dx.doi.org/10.1134/s107042801810010x.
Повний текст джерелаBanwell, MG, JM Cameron, M. Corbett, JR Dupuche, E. Hamel, JN Lambert, CM Lin, and MF Mackay. "Synthesis and Tubulin-Binding Properties of Some AC- and ABC-Ring Analogs of Allocolchicine." Australian Journal of Chemistry 45, no. 12 (1992): 1967. http://dx.doi.org/10.1071/ch9921967.
Повний текст джерелаDjurdjevic, Sinisa, Fei Yang, and James R. Green. "ChemInform Abstract: Intramolecular Nicholas Reactions in the Synthesis of Dibenzocycloheptanes. Synthesis of Allocolchicine NSC 51046 (IVa) and Analogues and the Formal Synthesis of (-)-Allocolchicine (V)." ChemInform 42, no. 11 (February 17, 2011): no. http://dx.doi.org/10.1002/chin.201111108.
Повний текст джерелаJoncour, Agnès, Anne Décor, Jian-Miao Liu, Marie-Elise Tran Huu Dau, and Olivier Baudoin. "Asymmetric Synthesis of Antimicrotubule Biaryl Hybrids of Allocolchicine and Steganacin." Chemistry - A European Journal 13, no. 19 (June 25, 2007): 5450–65. http://dx.doi.org/10.1002/chem.200601764.
Повний текст джерелаKrasniqi, Besir, and Wim Dehaen. "Synthesis of 1,2,3-Triazolo-Fused Allocolchicine Analogs via Intramolecular Oxidative Biaryl Coupling." Organic Letters 21, no. 13 (June 26, 2019): 5002–5. http://dx.doi.org/10.1021/acs.orglett.9b01707.
Повний текст джерелаSitnikov, Nikolay, Janna Velder, Liliane Abodo, Nicole Cuvelier, Jörg Neudörfl, Aram Prokop, Günter Krause, Aleksey Y. Fedorov, and Hans-Günther Schmalz. "Total Synthesis of Indole-Derived Allocolchicine Analogues Exhibiting Strong Apoptosis-Inducing Activity." Chemistry - A European Journal 18, no. 38 (August 27, 2012): 12096–102. http://dx.doi.org/10.1002/chem.201200083.
Повний текст джерелаZhang, Yan, Zhenzhi Cai, Julia Struwe, Chanchan Ma, Wangyu Zeng, Xinyi Liao, Min Xu, and Lutz Ackermann. "Dibenzocycloheptanones construction through a removable P-centered radical: synthesis of allocolchicine analogues." Chemical Science 12, no. 47 (2021): 15727–32. http://dx.doi.org/10.1039/d1sc05404j.
Повний текст джерелаSitnikov, Nikolay S., Antonina S. Kokisheva, Georgy K. Fukin, Jörg-Martin Neudörfl, Hannah Sutorius, Aram Prokop, Valery V. Fokin, Hans-Günther Schmalz, and Alexey Yu Fedorov. "Synthesis of Indole-Derived Allocolchicine Congeners through Pd-Catalyzed Intramolecular C-H Arylation Reaction." European Journal of Organic Chemistry 2014, no. 29 (September 4, 2014): 6481–92. http://dx.doi.org/10.1002/ejoc.201402850.
Повний текст джерелаPaymode, Dinesh J., and Chepuri V. Ramana. "Total Synthesis of (±)-Allocolchicine and Its Analogues Using Co-Catalyzed Alkyne [2 + 2 + 2]-Cyclotrimerization." ACS Omega 2, no. 9 (September 8, 2017): 5591–600. http://dx.doi.org/10.1021/acsomega.7b00980.
Повний текст джерелаVorogushin, Andrei V., Alexander V. Predeus, William D. Wulff, and Hans-Jürgen Hansen. "Diels−Alder Reaction−Aromatization Approach toward Functionalized Ring C Allocolchicinoids. Enantioselective Total Synthesis of (−)-7S-Allocolchicine." Journal of Organic Chemistry 68, no. 15 (July 2003): 5826–31. http://dx.doi.org/10.1021/jo034420t.
Повний текст джерелаSchmalz, Hans-Günther, and Norman Nicolaus. "Synthesis of Novel Allocolchicine Analogues with a Pyridine C-Ring through Intermolecular Vollhardt Diyne-Nitrile Cyclotrimerization." Synlett 2010, no. 14 (July 22, 2010): 2071–74. http://dx.doi.org/10.1055/s-0030-1258512.
Повний текст джерелаBANWELL, M. G., J. M. CAMERON, M. CORBETT, J. R. DUPUCHE, E. HAMEL, J. N. LAMBERT, C. M. LIN, and M. F. MACKAY. "ChemInform Abstract: Synthesis and Tubulin-Binding Properties of Some AC- and ABC-Ring Analogues of Allocolchicine." ChemInform 24, no. 13 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199313279.
Повний текст джерелаSitnikov, Nikolay S., Antonina S. Kokisheva, Georgy K. Fukin, Joerg-Martin Neudoerfl, Hannah Sutorius, Aram Prokop, Valery V. Fokin, Hans-Guenther Schmalz, and Alexey Yu Fedorov. "ChemInform Abstract: Synthesis of Indole-Derived Allocolchicine Congeners Through Pd-Catalyzed Intramolecular C-H Arylation Reaction." ChemInform 46, no. 12 (March 2015): no. http://dx.doi.org/10.1002/chin.201512277.
Повний текст джерелаNicolaus, Norman, and Hans-Guenther Schmalz. "ChemInform Abstract: Synthesis of Novel Allocolchicine Analogues with a Pyridine C-Ring Through Intermolecular Vollhardt Diyne-Nitrile Cyclotrimerization." ChemInform 42, no. 2 (December 16, 2010): no. http://dx.doi.org/10.1002/chin.201102204.
Повний текст джерелаCorrie, Tom J. A., and Guy C. Lloyd-Jones. "Formal Synthesis of (±)-Allocolchicine Via Gold-Catalysed Direct Arylation: Implication of Aryl Iodine(III) Oxidant in Catalyst Deactivation Pathways." Topics in Catalysis 60, no. 8 (April 19, 2017): 570–79. http://dx.doi.org/10.1007/s11244-017-0742-z.
Повний текст джерелаBhowmik, Subhendu, Shruti Khanna, Kumkum Srivastava, Mohammad Hasanain, Jayanta Sarkar, Sandeep Verma, and Sanjay Batra. "An Efficient Combinatorial Synthesis of Allocolchicine Analogues via a Triple Cascade Reaction and their Evaluation as Inhibitors of Insulin Aggregation." ChemMedChem 8, no. 11 (September 5, 2013): 1767–72. http://dx.doi.org/10.1002/cmdc.201300302.
Повний текст джерелаCorrie, Tom J. A., and Guy C. Lloyd-Jones. "Correction to: Formal Synthesis of (±)-Allocolchicine Via Gold-Catalysed Direct Arylation: Implication of Aryl Iodine(III) Oxidant in Catalyst Deactivation Pathways." Topics in Catalysis 63, no. 19-20 (February 24, 2020): 1766. http://dx.doi.org/10.1007/s11244-020-01243-w.
Повний текст джерелаBhowmik, Subhendu, Shruti Khanna, Kumkum Srivastava, Mohammad Hasanain, Jayanta Sarkar, Sandeep Verma, and Sanjay Batra. "ChemInform Abstract: An Efficient Combinatorial Synthesis of Allocolchicine Analogues via a Triple Cascade Reaction and Their Evaluation as Inhibitors of Insulin Aggregation." ChemInform 45, no. 13 (March 14, 2014): no. http://dx.doi.org/10.1002/chin.201413048.
Повний текст джерелаDjurdjevic, Sinisa, and James R. Green. "Allocolchicines via Intramolecular Nicholas Reactions: The Synthesis of NSC 51046." Organic Letters 9, no. 26 (December 2007): 5505–8. http://dx.doi.org/10.1021/ol7024422.
Повний текст джерелаBoyer, François-Didier, and Issam Hanna. "Synthesis of Allocolchicines Using Sequential Ring-Closing Enyne Metathesis−Diels−Alder Reactions." Organic Letters 9, no. 4 (February 2007): 715–18. http://dx.doi.org/10.1021/ol0630548.
Повний текст джерелаJain, Nishant, Divya Yada, Thokhir B. Shaik, Galanki Vasantha, P. Surendra Reddy, Shasi V. Kalivendi, and B. Sreedhar. "Synthesis and Antitumor Evaluation of Nitrovinyl Biphenyls: Anticancer Agents Based on Allocolchicines." ChemMedChem 6, no. 5 (April 6, 2011): 859–68. http://dx.doi.org/10.1002/cmdc.201100019.
Повний текст джерелаGracheva, Iuliia A., Hans Günther Schmalz, Elena V. Svirshchevskaya, Ekaterina S. Shchegravina, and Alexey Fedorov. "Design of an Aryne-Platform for the Synthesis of Non-Racemic Heterocyclic Allocolchicinoids." Organic & Biomolecular Chemistry, 2023. http://dx.doi.org/10.1039/d3ob00827d.
Повний текст джерела"Synthesis of Allocolchicine Analogues through Construction and Removal of P-centered Radicals." Synfacts 18, no. 03 (February 16, 2022): 0251. http://dx.doi.org/10.1055/s-0041-1737884.
Повний текст джерелаPollok, Dennis, Florian U. Rausch, Sebastian B. Beil, Peter Franzmann, and Siegfried R. Waldvogel. "Allocolchicines─Synthesis with Electro-organic Key Transformations." Organic Letters, May 3, 2022. http://dx.doi.org/10.1021/acs.orglett.2c01084.
Повний текст джерелаDjurdjevic, Sinisa, and James R. Green. "ChemInform Abstract: Allocolchicines via Intramolecular Nicholas Reactions: The Synthesis of NSC 51046." ChemInform 39, no. 22 (May 27, 2008). http://dx.doi.org/10.1002/chin.200822201.
Повний текст джерелаBoyer, Francois-Didier, and Issam Hanna. "Synthesis of Allocolchicines Using Sequential Ring-Closing Enyne Metathesis—Diels—Alder Reactions." ChemInform 38, no. 26 (June 26, 2007). http://dx.doi.org/10.1002/chin.200726160.
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