Artículos de revistas sobre el tema "241D"
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Murali, R. V. N. S. y S. Chandrasekhar. "Stereocontrolled synthesis of piperidine alkaloids, (−)-241D and (−)-isosolenopsin". Tetrahedron Letters 53, n.º 27 (julio de 2012): 3467–70. http://dx.doi.org/10.1016/j.tetlet.2012.04.115.
Texto completoCiblat, Stéphane, Pierre Calinaud, Jean-Louis Canet y Yves Troin. "A simple synthesis of (+)- and (−)-alkaloid 241D and C-4 epimers". Journal of the Chemical Society, Perkin Transactions 1, n.º 3 (2000): 353–57. http://dx.doi.org/10.1039/a908265d.
Texto completoSaha, Nemai y Shital K. Chattopadhyay. "Enantiodivergency and Enantioconvergency in the Synthesis of the Dendrobate Alkaloid 241D". Journal of Organic Chemistry 77, n.º 24 (11 de diciembre de 2012): 11056–63. http://dx.doi.org/10.1021/jo3019329.
Texto completoSateesh Chandra Kumar, R., G. Venkateswar Reddy, G. Shankaraiah, K. Suresh Babu y J. Madhusudana Rao. "Stereoselective synthesis of dendrobate alkaloid (+)-241D and its C-4 epimer". Tetrahedron Letters 51, n.º 7 (febrero de 2010): 1114–16. http://dx.doi.org/10.1016/j.tetlet.2009.12.111.
Texto completoGirard, Nicolas y Jean-Pierre Hurvois. "Anodic cyanation of C-4 hydroxylated piperidines: total synthesis of (±)-alkaloid 241D". Tetrahedron Letters 48, n.º 23 (junio de 2007): 4097–99. http://dx.doi.org/10.1016/j.tetlet.2007.04.010.
Texto completoYang, Yang. "Building polyfunctional piperidines: a stereoselective strategy of a three-component Mannich reaction inspired by biosynthesis and applications in the synthesis of natural alkaloids (+)-241D; (−)-241D; isosolenopsin A and (−)-epimyrtine". RSC Advances 5, n.º 24 (2015): 18894–908. http://dx.doi.org/10.1039/c4ra14418j.
Texto completoCiblat, Stephane, Pierre Calinaud, Jean-Louis Canet y Yves Troin. "ChemInform Abstract: A Simple Synthesis of (+)- and (-)-Alkaloid 241D and C-4 Epimers." ChemInform 31, n.º 22 (8 de junio de 2010): no. http://dx.doi.org/10.1002/chin.200022193.
Texto completoYang, Yang. "ChemInform Abstract: Building Polyfunctional Piperidines: A Stereoselective Strategy of a Three-Component Mannich Reaction Inspired by Biosynthesis and Applications in the Synthesis of Natural Alkaloids (+)-241D; (-)-241D; Isosolenopsin A and (-)-Epimyrti". ChemInform 46, n.º 28 (25 de junio de 2015): no. http://dx.doi.org/10.1002/chin.201528260.
Texto completoGouault, Nicolas, Myriam Le Roch, Gisele de Campos Pinto y Michèle David. "Total synthesis of dendrobate alkaloid (+)-241D, isosolenopsin and isosolenopsin A: application of a gold-catalyzed cyclization". Organic & Biomolecular Chemistry 10, n.º 29 (2012): 5541. http://dx.doi.org/10.1039/c2ob25685a.
Texto completoMonfray, Jérémy, Yvonne Gelas-Mialhe, Jean-Claude Gramain y Roland Remuson. "A new asymmetric synthesis of 2,6-cis-disubstituted 4-methylenepiperidines: total synthesis of (+)-alkaloid 241D and (+)-isosolenopsin A". Tetrahedron: Asymmetry 16, n.º 5 (marzo de 2005): 1025–34. http://dx.doi.org/10.1016/j.tetasy.2005.01.018.
Texto completoChênevert, Robert y Michael Dickman. "Enzymatic Route to Chiral, Nonracemiccis-2,6- andcis,cis-2,4,6-Substituted Piperidines. Synthesis of (+)-Dihydropinidine and Dendrobate Alkaloid (+)-241D". Journal of Organic Chemistry 61, n.º 10 (enero de 1996): 3332–41. http://dx.doi.org/10.1021/jo9519569.
Texto completoHarkiss, Alexander H. y Andrew Sutherland. "Access to 2,6-Disubstituted 4-Oxopiperidines Using a 6-Endo-trig Cyclization: Stereoselective Synthesis of Spruce Alkaloid and (+)-241D". Journal of Organic Chemistry 83, n.º 1 (18 de diciembre de 2017): 535–42. http://dx.doi.org/10.1021/acs.joc.7b02799.
Texto completoDas, Biswanath y Kongara Damodar. "(N-tert-Butanesulfinyl)imines in Alkaloid Synthesis: Concise Formal Syntheses of the Dendrobate Alkaloid (+)-241D and Its C-4 Epimer¹". Synthesis 44, n.º 01 (2 de diciembre de 2011): 83–86. http://dx.doi.org/10.1055/s-0031-1289634.
Texto completoKhandare, Sopan P., Polimera Obula Reddy y Kavirayani R. Prasad. "Addition of Lithium Anion of (Acetylmethylene)triphenylphosphorane to Nonracemic Sulfinimines: Total Synthesis of (+)-241D and Formal Total Synthesis of (+)-Preussin". Organic Letters 22, n.º 18 (27 de agosto de 2020): 7273–77. http://dx.doi.org/10.1021/acs.orglett.0c02608.
Texto completoMa, Dawei y Haiying Sun. "A Simple and Stereospecfic Route to 2,6-Disubstituted 4-Hydroxypiperidines. Synthesis of Dendrobate Alkaloid (+)-241D and Formal Synthesis of (−)-Indolizidine 167B". Organic Letters 2, n.º 16 (agosto de 2000): 2503–5. http://dx.doi.org/10.1021/ol006176n.
Texto completoEdwards, Michael W., H. Martin Garraffo y John W. Daly. "Facile Synthesis of 4-Piperidones by Condensation of an α,β-Unsaturated Ketone, an Aldehyde and Ammonia: Synthesis of theDendrobatidFrog Alkaloid 241D". Synthesis 1994, n.º 11 (1994): 1167–70. http://dx.doi.org/10.1055/s-1994-25665.
Texto completoDavis, Franklin A., Bin Chao y Ashwin Rao. "Intramolecular Mannich Reaction in the Asymmetric Synthesis of Polysubstituted Piperidines: Concise Synthesis of the Dendrobate Alkaloid (+)-241D and Its C-4 Epimer". Organic Letters 3, n.º 20 (octubre de 2001): 3169–71. http://dx.doi.org/10.1021/ol0164839.
Texto completoAbrunhosa-Thomas, Isabelle, Aurélie Plas, Alexandre Vogrig, Nishanth Kandepedu, Pierre Chalard y Yves Troin. "Access to 2,6-Disubstituted Piperidines: Control of the Diastereoselectivity, Scope, and Limitations. Applications to the Stereoselective Synthesis of (−)-Solenopsine A and Alkaloid (+)-241D". Journal of Organic Chemistry 78, n.º 6 (28 de febrero de 2013): 2511–26. http://dx.doi.org/10.1021/jo302712f.
Texto completoCHENEVERT, R. y M. DICKMAN. "ChemInform Abstract: Enzymatic Route to Chiral, Nonracemic cis-2,6- and cis,cis-2,4,6- Substituted Piperidines. Synthesis of (+)-Dihydropinidine (VI) and Dendrobate Alkaloid (+)-241D (VII)." ChemInform 27, n.º 37 (5 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199637193.
Texto completoAbrunhosa-Thomas, Isabelle, Aurelie Plas, Alexandre Vogrig, Nishanth Kandepedu, Pierre Chalard y Yves Troin. "ChemInform Abstract: Access to 2,6-Disubstituted Piperidines: Control of the Diastereoselectivity, Scope, and Limitations. Applications to the Stereoselective Synthesis of (-)-Solenopsine A and Alkaloid (+)-241D." ChemInform 44, n.º 30 (4 de julio de 2013): no. http://dx.doi.org/10.1002/chin.201330164.
Texto completoMa, Dawei y Haiying Sun. "ChemInform Abstract: A Simple and Stereospecific Route to 2,6-Disubstituted 4-Hydroxypiperidines. Synthesis of Dendrobate Alkaloid (+)-241D (XII) and Formal Synthesis of (-)-Indolizidine 167B (XVII)." ChemInform 31, n.º 45 (7 de noviembre de 2000): no. http://dx.doi.org/10.1002/chin.200045155.
Texto completoKazi, Aslamuzzaman, Adam Carie, Michelle A. Blaskovich, Cynthia Bucher, Van Thai, Stacy Moulder, Hairuo Peng et al. "Blockade of Protein Geranylgeranylation Inhibits Cdk2-Dependent p27Kip1 Phosphorylation on Thr187 and Accumulates p27Kip1 in the Nucleus: Implications for Breast Cancer Therapy". Molecular and Cellular Biology 29, n.º 8 (9 de febrero de 2009): 2254–63. http://dx.doi.org/10.1128/mcb.01029-08.
Texto completoVu, Van Ha, Fadila Louafi, Nicolas Girard, Ronan Marion, Thierry Roisnel, Vincent Dorcet y Jean-Pierre Hurvois. "Electrochemical Access to 8-(1-Phenyl-ethyl)-1,4-dioxa-8-aza-spiro[4.5]decane-7-carbonitrile. Application to the Asymmetric Syntheses of (+)-Myrtine and Alkaloid (+)-241D". Journal of Organic Chemistry 79, n.º 8 (3 de abril de 2014): 3358–73. http://dx.doi.org/10.1021/jo500104c.
Texto completoDavis, Franklin A., Bin Chao y Ashwin Rao. "ChemInform Abstract: Intramolecular Mannich Reaction in the Asymmetric Synthesis of Polysubstituted Piperidines: Concise Synthesis of the Dendrobate Alkaloid (+)-241D (I) and Its C-4 Epimer (II)." ChemInform 33, n.º 5 (23 de mayo de 2010): no. http://dx.doi.org/10.1002/chin.200205207.
Texto completoEDWARDS, M. W., H. M. GARRAFFO y J. W. DALY. "ChemInform Abstract: Facile Synthesis of 4-Piperidones by Condensation of an α,β- Unsaturated Ketone, an Aldehyde and Ammonia: Synthesis of the Dendrobatid Frog Alkaloid 241D (XII)." ChemInform 26, n.º 18 (18 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199518264.
Texto completoVu, Van Ha, Fadila Louafi, Nicolas Girard, Ronan Marion, Thierry Roisnel, Vincent Dorcet y Jean-Pierre Hurvois. "ChemInform Abstract: Electrochemical Access to 8-(1-Phenyl-ethyl)-1,4-dioxa-8-aza-spiro[4.5]decane-7-carbonitrile. Application to the Asymmetric Syntheses of (+)-Myrtine and Alkaloid (+)-241D." ChemInform 45, n.º 41 (25 de septiembre de 2014): no. http://dx.doi.org/10.1002/chin.201441210.
Texto completoHu, Mingxing, Chao Yang, Yi Luo, Fan Chen, Fangfang Yang, Shuping Yang, Hao Chen, Zhiqiang Cheng, Kun Li y Yongmei Xie. "Correction: A hypoxia-specific and mitochondria-targeted anticancer theranostic agent with high selectivity for cancer cells". Journal of Materials Chemistry B 6, n.º 26 (2018): 4385. http://dx.doi.org/10.1039/c8tb90081g.
Texto completoLangyan, Sapna, Zahoor A. Dar, D. P. Chaudhary, J. C. Shekhar, Susila Herlambang, Hesham El Enshasy, R. Z. Sayyed y S. Rakshit. "Analysis of Nutritional Quality Attributes and Their Inter-Relationship in Maize Inbred Lines for Sustainable Livelihood". Sustainability 13, n.º 11 (29 de mayo de 2021): 6137. http://dx.doi.org/10.3390/su13116137.
Texto completoWeng, Leiyun, Yuichi Hirata, Masaaki Arai, Michinori Kohara, Takaji Wakita, Koichi Watashi, Kunitada Shimotohno, Ying He, Jin Zhong y Tetsuya Toyoda. "Sphingomyelin Activates Hepatitis C Virus RNA Polymerase in a Genotype-Specific Manner". Journal of Virology 84, n.º 22 (15 de septiembre de 2010): 11761–70. http://dx.doi.org/10.1128/jvi.00638-10.
Texto completoSriratanasak, Nicharat, Worawat Wattanathana y Pithi Chanvorachote. "6,6′-((Methylazanedyl)bis(methylene))bis(2,4-dimethylphenol) Induces Autophagic Associated Cell Death through mTOR-Mediated Autophagy in Lung Cancer". Molecules 27, n.º 19 (22 de septiembre de 2022): 6230. http://dx.doi.org/10.3390/molecules27196230.
Texto completoReddy, Arava Amaranadha, Polimera Obula Reddy y Kavirayani R. Prasad. "Synthesis of β-Amino-Substituted Enones by Addition of Substituted Methyl Enones to Sulfinimines: Application to the Total Synthesis of Alkaloids (+)-Lasubine II and (+)-241D and the Formal Total Synthesis of (−)-Lasubine I". Journal of Organic Chemistry 81, n.º 22 (20 de octubre de 2016): 11363–71. http://dx.doi.org/10.1021/acs.joc.6b01541.
Texto completoGao, X., S. Lester, B. Matheson, B. Boettcher y J. McCluskey. "Three newly identified A*24 alleles: A*2406, A*2413 and A*2414". Tissue Antigens 50, n.º 2 (agosto de 1997): 192–96. http://dx.doi.org/10.1111/j.1399-0039.1997.tb02858.x.
Texto completoComstock, Laurie E. "Small RNAs Repress Expression of Polysaccharide Utilization Loci of Gut Bacteroides Species". Journal of Bacteriology 198, n.º 18 (11 de julio de 2016): 2396–98. http://dx.doi.org/10.1128/jb.00514-16.
Texto completoA. Nikulin, Andrey. "The Object of the Right Concept for State Ownership of Land". HELIX 8, n.º 01 (1 de enero de 2018): 2411–14. http://dx.doi.org/10.29042/2018-2411-2414.
Texto completoYu. Tumanov, Dmitriy. "The Conscience of the Jury as a Basis for Delivering a Fair Verdict in Accordance with the Judicial Reform of 1864 in Russia (Historico-Juridical Research)". HELIX 8, n.º 01 (1 de enero de 2018): 2415–19. http://dx.doi.org/10.29042/2018-2415-2419.
Texto completo&NA;. "2411". Medicine & Science in Sports & Exercise 37, Supplement (mayo de 2005): S461. http://dx.doi.org/10.1249/00005768-200505001-02411.
Texto completo&NA;. "2417". Medicine & Science in Sports & Exercise 37, Supplement (mayo de 2005): S463. http://dx.doi.org/10.1249/00005768-200505001-02417.
Texto completo&NA;. "2411". Medicine & Science in Sports & Exercise 37, Supplement (mayo de 2005): S461. http://dx.doi.org/10.1097/00005768-200505001-02411.
Texto completo&NA;. "2417". Medicine & Science in Sports & Exercise 37, Supplement (mayo de 2005): S463. http://dx.doi.org/10.1097/00005768-200505001-02417.
Texto completoHirata, M., S. Araki, T. Hirai, H. Ohishi y T. Jibiki. "2410". Ultrasound in Medicine & Biology 32, n.º 5 (mayo de 2006): P174—P175. http://dx.doi.org/10.1016/j.ultrasmedbio.2006.02.706.
Texto completoMarcelino, A., M. Pinho, P. Viana, O. Saito, A. de Oliveira, M. Chammas y G. Cerri. "2411". Ultrasound in Medicine & Biology 32, n.º 5 (mayo de 2006): P175. http://dx.doi.org/10.1016/j.ultrasmedbio.2006.02.707.
Texto completoChoi, J. Y., J. Y. Lee, J. M. Lee, S. H. Kim, M. W. Lee, J. K. Han y B. I. Choi. "2413". Ultrasound in Medicine & Biology 32, n.º 5 (mayo de 2006): P175. http://dx.doi.org/10.1016/j.ultrasmedbio.2006.02.708.
Texto completoLi, R., Y. Guo, X. Hua, J. Ding, A. Guo y X. Zhang. "2414". Ultrasound in Medicine & Biology 32, n.º 5 (mayo de 2006): P175—P176. http://dx.doi.org/10.1016/j.ultrasmedbio.2006.02.710.
Texto completoKim, S. Y., K. W. Kim, S. H. Park, S. S. Lee, Y. M. Shin, P. N. Kim, M. G. Lee y S. G. Lee. "2415". Ultrasound in Medicine & Biology 32, n.º 5 (mayo de 2006): P176. http://dx.doi.org/10.1016/j.ultrasmedbio.2006.02.711.
Texto completoLee, S. S., K. W. Kim, S. H. Park, J. H. Byun, Y. M. Shin, H. J. Won, A. Y. Kim, P. N. Kim, M. G. Lee y H. K. Ha. "2416". Ultrasound in Medicine & Biology 32, n.º 5 (mayo de 2006): P176. http://dx.doi.org/10.1016/j.ultrasmedbio.2006.02.712.
Texto completoLee, S. S., K. W. Kim, S. H. Park, Y. M. Shin, J. H. Byun, H. J. Won, A. Y. Kim, P. N. Kim, M. G. Lee y H. K. Ha. "2417". Ultrasound in Medicine & Biology 32, n.º 5 (mayo de 2006): P176. http://dx.doi.org/10.1016/j.ultrasmedbio.2006.02.713.
Texto completoZhang, Q., Z. Wang, H. Ran, X. Fu y X. Li. "2418". Ultrasound in Medicine & Biology 32, n.º 5 (mayo de 2006): P176. http://dx.doi.org/10.1016/j.ultrasmedbio.2006.02.714.
Texto completoRan, H., H. Ren, Z. Wang, Y. Zheng, Q. Zhang y C. Xu. "2419". Ultrasound in Medicine & Biology 32, n.º 5 (mayo de 2006): P176—P177. http://dx.doi.org/10.1016/j.ultrasmedbio.2006.02.715.
Texto completoMartin, Michelle. "2411". Medicine & Science in Sports & Exercise 48 (mayo de 2016): 660–61. http://dx.doi.org/10.1249/01.mss.0000486980.95766.88.
Texto completoWhitt-Glover, Melicia C. "2419". Medicine & Science in Sports & Exercise 48 (mayo de 2016): 663. http://dx.doi.org/10.1249/01.mss.0000486988.72002.54.
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