Artículos de revistas sobre el tema "Stereoselective reaction"
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Misra, Anup Kumar, Arin Gucchait y Monalisa Kundu. "Synthesis of Pentasaccharide Repeating Unit Corresponding to the Cell Wall O-Polysaccharide of Salmonella enterica O55 Strain Containing a Rare Sugar 3-Acetamido-3-deoxy-d-fucose". Synthesis 53, n.º 19 (24 de junio de 2021): 3613–20. http://dx.doi.org/10.1055/s-0037-1610777.
Texto completoRossi, Sergio, Tiziana Benincori, Laura Maria Raimondi y Maurizio Benaglia. "3,3′-Bithiophene-Based Chiral Bisphosphine Oxides as Organocatalysts in Silicon-Derived Lewis Acid Mediated Reactions". Synlett 31, n.º 06 (7 de enero de 2020): 535–46. http://dx.doi.org/10.1055/s-0039-1690777.
Texto completoKlegraf, Ellen y Horst Kunz. "Stereoselective Synthesis of 3-Substituted and 3,4-Disubstituted Piperidine und Piperidin-2-one Derivatives". Zeitschrift für Naturforschung B 67, n.º 4 (1 de abril de 2012): 389–405. http://dx.doi.org/10.1515/znb-2012-0413.
Texto completoWoo, Simon, Masood Parvez y Brian A. Keay. "Regio- and stereoselective ring openings of unsymmetrical oxatricyclo adducts". Canadian Journal of Chemistry 75, n.º 6 (1 de junio de 1997): 665–80. http://dx.doi.org/10.1139/v97-081.
Texto completoPenumati, Nageshwar Rao y Nagaiah Kommu. "Stereoselective Synthesis of (+)-α-Conhydrine from R-(+)-Glyceraldehyde". Organic Chemistry International 2014 (20 de octubre de 2014): 1–7. http://dx.doi.org/10.1155/2014/982716.
Texto completoSchultz, Jeremy F., Bing Yang y Nan Jiang. "Direct observation of the geometric isomer selectivity of a reaction controlled via adsorbed bromine". Nanoscale 12, n.º 4 (2020): 2726–31. http://dx.doi.org/10.1039/c9nr09857g.
Texto completoLiu, Yuxiao, Yongming Deng, Peter Y. Zavalij, Renhua Liu y Michael P. Doyle. "An efficient route to highly enantioenriched tetrahydroazulenes and β-tetralones by desymmetrization reactions of δ,δ-diaryldiazoaceto-acetates". Chemical Communications 51, n.º 3 (2015): 565–68. http://dx.doi.org/10.1039/c4cc08255a.
Texto completoRoss, Günther y Ivar Ugi. "Stereoselective syntheses of α-amino acid and peptide derivatives by the U-4CR of 5-desoxy-5-thio-D-xylopyranosylamine". Canadian Journal of Chemistry 79, n.º 12 (1 de diciembre de 2001): 1934–39. http://dx.doi.org/10.1139/v01-186.
Texto completoCantin, Michel, Yao-Chang Xu y Pierre Deslongchamps. "Stereocontrolled construction of A.B.C.[6.6.6] tricycle via transannular Diels–Alder reaction of 14-membered triene macrocycle". Canadian Journal of Chemistry 68, n.º 12 (1 de diciembre de 1990): 2144–52. http://dx.doi.org/10.1139/v90-329.
Texto completoSugita, Kazuyuki, Motoi Kuwabara, Ami Matsuo, Shogo Kamo y Akinobu Matsuzawa. "Stereoselective Convergent Synthesis of Carbon Skeleton of Cotylenin A Aglycone". Synthesis 53, n.º 12 (1 de febrero de 2021): 2092–102. http://dx.doi.org/10.1055/s-0040-1706684.
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 completoYajima, Tomoko, Eriko Yoshida y Masako Hamano. "Diastereoselective radical addition to γ-alkyl-α-methylene-γ-butyrolactams and the synthesis of a chiral pyroglutamic acid derivative". Beilstein Journal of Organic Chemistry 9 (17 de julio de 2013): 1432–36. http://dx.doi.org/10.3762/bjoc.9.161.
Texto completoFischer, Róbert, Ondrej Záborský, Radka Štadániová, Jana Doháňošová y Ján Moncol. "Synthesis of Isoxazolidinyl Epoxides by Oxone Treatment of 2,3-Dihydroisoxazoles in Acetone–Water Solution: A New Stereoselective Approach to Hydroxy-Substituted Isoxazolidines". Synthesis 49, n.º 22 (27 de septiembre de 2017): 4942–54. http://dx.doi.org/10.1055/s-0036-1590924.
Texto completoShindo, M. y K. Yaji. "Scandium-Catalyzed Stereoselective Nazarov Reaction". Synfacts 2009, n.º 12 (20 de noviembre de 2009): 1358. http://dx.doi.org/10.1055/s-0029-1218236.
Texto completoRiant, O., O. Chuzel, J. Deschamps y C. Chausteur. "Stereoselective Tandem Reductive Aldol Reaction". Synfacts 2007, n.º 3 (marzo de 2007): 0313. http://dx.doi.org/10.1055/s-2007-968183.
Texto completoGangadhar, Pamarthi, Sayini Ramakrishna, Ponneri Venkateswarlu y Pabbaraja Srihari. "Stereoselective total synthesis and structural revision of the diacetylenic diol natural products strongylodiols H and I". Beilstein Journal of Organic Chemistry 14 (4 de septiembre de 2018): 2313–20. http://dx.doi.org/10.3762/bjoc.14.206.
Texto completoJanzen, Alexander F. y Meehae Jang. "Isomerization, fluorine exchange, and stereoselective synthesis of cis- and trans-F2TePh3Cl: application of the coordination model of reaction mechanisms". Canadian Journal of Chemistry 67, n.º 1 (1 de enero de 1989): 71–75. http://dx.doi.org/10.1139/v89-012.
Texto completoEscalante, Carlos H., Eder I. Martínez-Mora, Carlos Espinoza-Hicks, Alejandro A. Camacho-Dávila, Fernando R. Ramos-Morales, Francisco Delgado y Joaquín Tamariz. "Highly selective Diels–Alder and Heck arylation reactions in a divergent synthesis of isoindolo- and pyrrolo-fused polycyclic indoles from 2-formylpyrrole". Beilstein Journal of Organic Chemistry 16 (17 de junio de 2020): 1320–34. http://dx.doi.org/10.3762/bjoc.16.113.
Texto completoPereira, Ana Margarida, Honorina Cidade y Maria Elizabeth Tiritan. "Stereoselective Synthesis of Flavonoids: A Brief Overview". Molecules 28, n.º 1 (3 de enero de 2023): 426. http://dx.doi.org/10.3390/molecules28010426.
Texto completoFeng, Xiujuan, Haixia Zhang, Wenbo Lu, Yoshinori Yamamoto, Abdulrahman Almansour, Natarajan Arumugam, Raju Kumar y Ming Bao. "Stereoselective Synthesis of Vinyl Iodides through Copper(I)-Catalyzed Finkelstein-Type Halide-Exchange Reaction". Synthesis 49, n.º 12 (11 de abril de 2017): 2727–32. http://dx.doi.org/10.1055/s-0036-1588988.
Texto completoSmetanin, N. V., S. A. Varenichenko, A. V. Mazepa, O. K. Farat, A. V. Kharchenko y V. I. Markov. "Atom-economic Michael reaction between hydroacridines and arylmaleimides without catalyst/additive". Voprosy Khimii i Khimicheskoi Tekhnologii, n.º 5 (octubre de 2022): 102–9. http://dx.doi.org/10.32434/0321-4095-2022-144-5-102-109.
Texto completoDarvesh, Sultan, Andrew S. Grant, David I. Magee y Zdenek Valenta. "An approach to the synthesis of bruceantin. The synthesis of a tetracyclic intermediate". Canadian Journal of Chemistry 67, n.º 12 (1 de diciembre de 1989): 2237–40. http://dx.doi.org/10.1139/v89-348.
Texto completoKarak, Milandip, Luiz C. A. Barbosa, Jaime A. M. Acosta, Ariel M. Sarotti y John Boukouvalas. "Thermodynamically driven, syn-selective vinylogous aldol reaction of tetronamides". Organic & Biomolecular Chemistry 14, n.º 21 (2016): 4897–907. http://dx.doi.org/10.1039/c6ob00895j.
Texto completoClark, J. Stephen y Michael Popadynec. "Stereoselective Synthesis of the I–L Fragment of the Pacific Ciguatoxins". Toxins 12, n.º 12 (24 de noviembre de 2020): 740. http://dx.doi.org/10.3390/toxins12120740.
Texto completoTarui, Atsushi, Yukiko Karuo, Kazuyuki Sato, Kentaro Kawai y Masaaki Omote. "Stereoselective Synthesis of Multisubstituted α-fluoro-β-lactams". Current Organic Chemistry 24, n.º 18 (18 de noviembre de 2020): 2169–80. http://dx.doi.org/10.2174/1385272824666200221114707.
Texto completoSoorukram, Darunee, Manat Pohmakotr, Chutima Kuhakarn y Vichai Reutrakul. "Stereoselective Synthesis of Tetrahydrofuran Lignans". Synthesis 50, n.º 24 (2 de octubre de 2018): 4746–64. http://dx.doi.org/10.1055/s-0037-1610289.
Texto completoSingh, Nidhi y Jaya Pandey. "Advances in Henry Reaction: A Versatile Method in Organic Synthesis". Mini-Reviews in Organic Chemistry 17, n.º 3 (28 de abril de 2020): 297–308. http://dx.doi.org/10.2174/1570193x16666190214150144.
Texto completoGualandi, Andrea, Luca Mengozzi y Pier Cozzi. "Stereoselective SN1-Type Reaction of Enols and Enolates". Synthesis 49, n.º 15 (13 de junio de 2017): 3433–43. http://dx.doi.org/10.1055/s-0036-1588871.
Texto completoBaikadi, Karunakar, Anil Talakokkula y A. Narsaiah. "Stereoselective Total Synthesis of Macrolide Sch-725674 and C-7-epi-Sch-725674". SynOpen 03, n.º 01 (enero de 2019): 26–35. http://dx.doi.org/10.1055/s-0037-1611665.
Texto completoLiu, Yingchun, Ted S. Sorensen y Fang Sun. "Stereoselective 1,3-debromination reactions". Canadian Journal of Chemistry 71, n.º 2 (1 de febrero de 1993): 258–62. http://dx.doi.org/10.1139/v93-037.
Texto completoSoto, Martín, Irene Sanz-Machín, Humberto Rodríguez-Solla y Vicente Gotor-Fernández. "Chemoenzymatic Stereoselective Synthesis of trans-Flavan-4-ols via Lipase-Catalyzed Kinetic Resolutions". Catalysts 11, n.º 11 (27 de octubre de 2021): 1296. http://dx.doi.org/10.3390/catal11111296.
Texto completoKhrimyan, Ashot P., Oganes A. Gharibyan, Ludvík Streinz, Zdeněk Wimmer, Miroslav Romaňuk y Shaliko O. Badanyan. "The hydroalumination-iodination of enyne α-alcohols: Synthesis of 3-methyl-2,4-alkadien-1-ols". Collection of Czechoslovak Chemical Communications 54, n.º 12 (1989): 3284–93. http://dx.doi.org/10.1135/cccc19893284.
Texto completoMarin, Lucile, Soufyan Jerhaoui, Emilie Kolodziej, Régis Guillot, Vincent Gandon, Françoise Colobert, Emmanuelle Schulz, Joanna Wencel‐Delord y David Lebœuf. "Sulfoxide‐Controlled Stereoselective Aza‐Piancatelli Reaction". Advanced Synthesis & Catalysis 363, n.º 17 (29 de julio de 2021): 4277–82. http://dx.doi.org/10.1002/adsc.202100848.
Texto completoBaba, A., S. Babu, M. Yasuda, Y. Okabe y I. Shibata. "Stereoselective Reformatsky Reaction of Indium Enolates". Synfacts 2006, n.º 9 (septiembre de 2006): 0930. http://dx.doi.org/10.1055/s-2006-949268.
Texto completoRama Rao, K., T. N. Srinivasan y N. Bhanumathi. "A stereoselective biocatalytic diels-alder reaction". Tetrahedron Letters 31, n.º 41 (enero de 1990): 5959–60. http://dx.doi.org/10.1016/s0040-4039(00)98004-3.
Texto completoByk, G. y E. Kabha. "A Solid-Supported Stereoselective Multicomponent Reaction". Synfacts 2006, n.º 7 (junio de 2006): 0739. http://dx.doi.org/10.1055/s-2006-941902.
Texto completoBauer, Adriano y Nuno Maulide. "A Stereoselective Reductive Hosomi–Sakurai Reaction". Organic Letters 20, n.º 5 (22 de febrero de 2018): 1461–64. http://dx.doi.org/10.1021/acs.orglett.8b00276.
Texto completoKapa, Prasad, Chen Kau-Ming, Repic Oljan y Hardtmann E. Goetz. "Stereoselective aldol reaction with chiral acetates". Tetrahedron: Asymmetry 1, n.º 10 (enero de 1990): 703–6. http://dx.doi.org/10.1016/s0957-4166(00)82378-2.
Texto completoRoy, Tamal, Myungjo J. Kim, Yang Yang, Suyeon Kim, Gyumin Kang, Xinyi Ren, Anders Kadziola, Hee-Yoon Lee, Mu-Hyun Baik y Ji-Woong Lee. "Carbon Dioxide-Catalyzed Stereoselective Cyanation Reaction". ACS Catalysis 9, n.º 7 (mayo de 2019): 6006–11. http://dx.doi.org/10.1021/acscatal.9b01087.
Texto completoSANO, Shigeki. "Development of Highly Stereoselective Reactions Utilizing Heteroatoms : New Approach to the Stereoselective Horner-Wadsworth-Emmons Reaction". YAKUGAKU ZASSHI 120, n.º 5 (2000): 432–44. http://dx.doi.org/10.1248/yakushi1947.120.5_432.
Texto completoGrigg, Ronald, Suren Husinec y Vladimir Savic. "Stereoselective cyclo-addition reactions of azomethine ylides catalysed by in situ generated Ag(I)/bisphosphine complexes". Journal of the Serbian Chemical Society 75, n.º 1 (2010): 1–9. http://dx.doi.org/10.2298/jsc1001001g.
Texto completoVarga, Eszter, László Tamás Mika, Antal Csámpai, Tamás Holczbauer, György Kardos y Tibor Soós. "Mechanistic investigations of a bifunctional squaramide organocatalyst in asymmetric Michael reaction and observation of stereoselective retro-Michael reaction". RSC Advances 5, n.º 115 (2015): 95079–86. http://dx.doi.org/10.1039/c5ra19593d.
Texto completoAitouna, Abdelhak Ouled, Ali Barhoumi y Abdellah Zeroual. "A Mechanism Study and an Investigation of the Reason for the Stereoselectivity in the [4+2] Cycloaddition Reaction between Cyclopentadiene and Gem-substituted Ethylene Electrophiles". Scientiae Radices 2, n.º 3 (27 de julio de 2023): 217–28. http://dx.doi.org/10.58332/scirad2023v2i3a01.
Texto completoBusfield, WK, DI Grice, ID Jenkins y SH Thang. "Reaction of t-Butoxy Radicals With Cyclic Alkenes Studied by the Nitroxide Radical-Trapping Technique". Australian Journal of Chemistry 44, n.º 10 (1991): 1407. http://dx.doi.org/10.1071/ch9911407.
Texto completoMinko, Yury, Morgane Pasco, Helena Chechik y Ilan Marek. "Regio- and stereoselective carbometallation reactions of N-alkynylamides and sulfonamides". Beilstein Journal of Organic Chemistry 9 (13 de marzo de 2013): 526–32. http://dx.doi.org/10.3762/bjoc.9.57.
Texto completoSingh, Surinderjit, M. PS Ishar, Gajendra Singh y Rajinder Singh. "Efficient, microwave-assisted intramolecular 1,3-dipolar cycloadditions of oximes and N-methylnitrones derived from o-alkenylmethoxy-acetophenones". Canadian Journal of Chemistry 83, n.º 3 (1 de marzo de 2005): 260–65. http://dx.doi.org/10.1139/v05-049.
Texto completoGhorai, Manas K., Subhomoy Das, Kalpataru Das y Amit Kumar. "Stereoselective synthesis of activated 2-arylazetidines via imino-aldol reaction". Organic & Biomolecular Chemistry 13, n.º 34 (2015): 9042–49. http://dx.doi.org/10.1039/c5ob01140j.
Texto completoVereshchagin, Anatoly N., Taigib M. Iliyasov, Kirill A. Karpenko, Radmir N. Akchurin y Mikhail E. Minyaev. "Tetrahydropyridines’ Stereoselective Formation, How Lockdown Assisted in the Identification of the Features of Its Mechanism". Molecules 27, n.º 14 (7 de julio de 2022): 4367. http://dx.doi.org/10.3390/molecules27144367.
Texto completoElinson, M. N., A. N. Vereshchagin, R. F. Nasybullin, S. I. Bobrovsky, A. I. Ilovaisky, V. M. Merkulova, I. S. Bushmarinov y M. P. Egorov. "General approach to a spiro indole-3,1′-naphthalene tetracyclic system: stereoselective pseudo four-component reaction of isatins and cyclic ketones with two molecules of malononitrile". RSC Advances 5, n.º 62 (2015): 50421–24. http://dx.doi.org/10.1039/c5ra03452c.
Texto completoAndreev, Mikhail V., Vladimir A. Potapov, Maxim V. Musalov y Lyudmila I. Larina. "A New Family of Vinyl Selenocyanates with the Amide Function Based on the Reaction of Potassium Selenocyanate with 3-Trimethylsilyl-2-Propynamides". Catalysts 13, n.º 9 (30 de agosto de 2023): 1257. http://dx.doi.org/10.3390/catal13091257.
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