Journal articles on the topic 'Sulfur heterocycles'
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Luna, Isadora Silva, Rayssa Marques Duarte da Cruz, Ryldene Marques Duarte da Cruz, Rodrigo Santos Aquino de Araújo, and Francisco Jaime Bezerra Mendonça-Junior. "1,4-Dithiane-2,5-diol: A Versatile Synthon for the Synthesis of Sulfur-containing Heterocycles." Current Organic Synthesis 15, no. 8 (December 17, 2018): 1026–42. http://dx.doi.org/10.2174/1570179415666180821154551.
Full textZhu, Yannan, and You Huang. "Organocatalyzed [3+3] Annulations for the Construction of Heterocycles." Synthesis 52, no. 08 (February 5, 2020): 1181–202. http://dx.doi.org/10.1055/s-0039-1690810.
Full textVasil'eva, T. P., V. M. Bystrova, and O. V. Kil'disheva. "Sulfur heterocycles." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 37, no. 7 (July 1988): 1448–55. http://dx.doi.org/10.1007/bf00962760.
Full textGarcía-Valverde, Maria, and Tomás Torroba. "Sulfur-Nitrogen Heterocycles." Molecules 10, no. 2 (February 28, 2005): 318–20. http://dx.doi.org/10.3390/10020318.
Full textSlivka, Mikhailo, and Mikhailo Onysko. "The Use of Electrophilic Cyclization for the Preparation of Condensed Heterocycles." Synthesis 53, no. 19 (May 19, 2021): 3497–512. http://dx.doi.org/10.1055/s-0040-1706036.
Full textRandić, Milan, Sonja Nikolić, and Nenad Trinajstić. "Aromaticity in heterocyclic molecules containing divalent sulfur." Collection of Czechoslovak Chemical Communications 53, no. 9 (1988): 2023–54. http://dx.doi.org/10.1135/cccc19882023.
Full textEngelhardt, Udo, and Andre Simon. "Phosphorus-Hydrazine-Sulfur-Heterocycles." Phosphorus, Sulfur, and Silicon and the Related Elements 65, no. 1-4 (February 1992): 65–67. http://dx.doi.org/10.1080/10426509208055319.
Full textR. StJ. Foreman, Mark, Josef Novosad, Alexandra M. Z. Slawin, and J. Derek Woollins. "New organophosphorus–sulfur heterocycles." Journal of the Chemical Society, Dalton Transactions, no. 8 (1997): 1347. http://dx.doi.org/10.1039/a608361g.
Full textSharma, Praveen Kumar. "A REVIEW: ANTIMICROBIAL AGENTS BASED ON NITROGEN AND SULFUR CONTAINING HETEROCYCLES." Asian Journal of Pharmaceutical and Clinical Research 10, no. 2 (February 1, 2017): 47. http://dx.doi.org/10.22159/ajpcr.2017.v10i2.15673.
Full textJourdain, F., and J. C. Pommelet. "Synthesis of New Sulfur Heterocycles." Synthetic Communications 27, no. 3 (February 1997): 483–92. http://dx.doi.org/10.1080/00397919708006050.
Full textZwanenburg, B., H. J. F. Philipse, M. M. H. Verstappen, and R. G. Gieling. "Sulfur substituted Small-ring Heterocycles." Phosphorus, Sulfur, and Silicon and the Related Elements 120, no. 1 (January 1, 1997): 453–54. http://dx.doi.org/10.1080/10426509708545594.
Full textSharma, Praveen K., Andleeb Amin, and M. Kumar. "A Review: Medicinally Important Nitrogen Sulphur Containing Heterocycles." Open Medicinal Chemistry Journal 14, no. 1 (September 14, 2020): 49–64. http://dx.doi.org/10.2174/1874104502014010049.
Full textGarcía-Valverde, María, and Tomás Torroba. "Heterocyclic Chemistry of Sulfur Chlorides – Fast Ways to Complex Heterocycles." European Journal of Organic Chemistry 2006, no. 4 (February 2006): 849–61. http://dx.doi.org/10.1002/ejoc.200500786.
Full textRakitin, Oleg A. "Synthesis and Reactivity of 3H-1,2-dithiole-3-thiones." Molecules 26, no. 12 (June 11, 2021): 3595. http://dx.doi.org/10.3390/molecules26123595.
Full textMajumdar, K. C., and A. K. Pal. "Lewis acid catalyzed Claisen rearrangement: Regioselective synthesis of oxygen, nitrogen, and sulfur heterocycles." Canadian Journal of Chemistry 86, no. 1 (January 1, 2008): 72–78. http://dx.doi.org/10.1139/v07-139.
Full textENGELHARDT, U., and A. SIMON. "ChemInform Abstract: Phosphorus-Hydrazine-Sulfur-Heterocycles." ChemInform 23, no. 25 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199225215.
Full textKnochel, P., M. Kienle, and A. Unsinn. "Synthesis of Sulfur Heterocycles from Dithiocarbamates." Synfacts 2010, no. 09 (August 23, 2010): 0992. http://dx.doi.org/10.1055/s-0030-1258001.
Full textGabillet, Sandra, Delphine Lecerclé,, Olivier Loreau, Michael Carboni, Sophie Dézard, Jean-Marie Gomis, and Frédéric Taran. "Phosphine-Catalyzed Construction of Sulfur Heterocycles." Organic Letters 9, no. 20 (September 2007): 3925–27. http://dx.doi.org/10.1021/ol701563e.
Full textTorroba, Tom?s. "Poly-sulfur-nitrogen heterocycles via sulfur chlorides and nitrogen reagents." Journal für praktische Chemie 341, no. 2 (February 1999): 99–113. http://dx.doi.org/10.1002/(sici)1521-3897(199902)341:2<99::aid-prac99>3.0.co;2-z.
Full textHudson, B. M., E. Nguyen, and D. J. Tantillo. "The influence of intramolecular sulfur–lone pair interactions on small-molecule drug design and receptor binding." Organic & Biomolecular Chemistry 14, no. 16 (2016): 3975–80. http://dx.doi.org/10.1039/c6ob00254d.
Full textKonstantinova, Lidia S., and Oleg A. Rakitin. "Design of sulfur heterocycles with sulfur monochloride: synthetic possibilities and prospects." Mendeleev Communications 19, no. 2 (March 2009): 55–61. http://dx.doi.org/10.1016/j.mencom.2009.03.001.
Full textBosset, Cyril, Gauthier Lefebvre, Patrick Angibaud, Ian Stansfield, Lieven Meerpoel, Didier Berthelot, Amandine Guérinot, and Janine Cossy. "Iron-Catalyzed Synthesis of Sulfur-Containing Heterocycles." Journal of Organic Chemistry 82, no. 8 (October 13, 2016): 4020–36. http://dx.doi.org/10.1021/acs.joc.6b01827.
Full textWillrodt, Imke, and Detlef Geffken. "Sulfur containing heterocycles from α-hydroxy-alkanimidates." European Journal of Pharmaceutical Sciences 4 (September 1996): S111. http://dx.doi.org/10.1016/s0928-0987(97)86334-8.
Full textKaur, Navjeet. "Solid-phase synthesis of sulfur containing heterocycles." Journal of Sulfur Chemistry 39, no. 5 (April 3, 2018): 544–77. http://dx.doi.org/10.1080/17415993.2018.1457673.
Full textJOURDAIN, F., and J. C. POMMELET. "ChemInform Abstract: Synthesis of New Sulfur Heterocycles." ChemInform 28, no. 26 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199726053.
Full textKobayashi, Keiji, Carl Th Pedersen, and Jan Becher. "Sulfur Heterocycles for Organic Conductors and Superconductors." Phosphorus, Sulfur, and Silicon and the Related Elements 43, no. 1-2 (May 1989): 187–208. http://dx.doi.org/10.1080/10426508908040285.
Full textCaserio, Marjorie C., and Jhong J. Kim. "Stereoelectronic Effects in Sulfur Heterocycles. Thiosulfonium Ions." Phosphorus and Sulfur and the Related Elements 23, no. 1-3 (June 1985): 169–95. http://dx.doi.org/10.1080/03086648508073385.
Full textMuhammad, Mohed Ahmad. "Physical Properties of Cyclestructure." American International Journal of Biology and Life Sciences 1, no. 1 (January 5, 2019): 15–22. http://dx.doi.org/10.46545/aijbls.v1i1.31.
Full textCampos and Berteina-Raboin. "Eucalyptol as a Bio-Based Solvent for Buchwald-Hartwig Reaction on O,S,N-Heterocycles." Catalysts 9, no. 10 (October 10, 2019): 840. http://dx.doi.org/10.3390/catal9100840.
Full textAly, Ashraf A., Alaa A. Hassan, Maysa M. Makhlouf, and Stefan Bräse. "Chemistry and Biological Activities of 1,2,4-Triazolethiones—Antiviral and Anti-Infective Drugs." Molecules 25, no. 13 (July 3, 2020): 3036. http://dx.doi.org/10.3390/molecules25133036.
Full textWoollins, J., Guoxiong Hua, David Cordes, and Alexandra Slawin. "Application of One-Pot Three-Component Condensation Reaction for the Synthesis of New Organophosphorus–Sulfur Macrocycles." Synlett 29, no. 11 (April 19, 2018): 1496–501. http://dx.doi.org/10.1055/s-0037-1609666.
Full textFan, Rong, Binbin Liu, Tianyu Zheng, Kun Xu, Chen Tan, Tianlong Zeng, Shuaisong Su, and Jiajing Tan. "An aryne triggered ring-opening fluorination of cyclic thioethers with potassium fluoride." Chemical Communications 54, no. 51 (2018): 7081–84. http://dx.doi.org/10.1039/c8cc03766c.
Full textZheng, Tianyu, Jiajing Tan, Rong Fan, Shuaisong Su, Binbin Liu, Chen Tan, and Kun Xu. "Diverse ring opening of thietanes and other cyclic sulfides: an electrophilic aryne activation approach." Chemical Communications 54, no. 11 (2018): 1303–6. http://dx.doi.org/10.1039/c7cc08553b.
Full textFeng, Wei, and Xing-Guo Zhang. "Organophosphine-free copper-catalyzed isothiocyanation of amines with sodium bromodifluoroacetate and sulfur." Chemical Communications 55, no. 8 (2019): 1144–47. http://dx.doi.org/10.1039/c8cc09190k.
Full textTorroba, Tomas. "ChemInform Abstract: Poly-Sulfur-Nitrogen Heterocycles via Sulfur Chlorides and Nitrogen Reagents." ChemInform 30, no. 18 (June 16, 2010): no. http://dx.doi.org/10.1002/chin.199918279.
Full textKrafft, Christoph, Stefan Brennecke, Frank Ott, Michael Backes, Reiner Salzer, Jörg Grunenberg, Jakob P Ley, Gerhard E Krammer, and Berthold Weber. "High‐Impact Sulfur Compounds: Constitutional and Configurational Assignment of Sulfur‐Containing Heterocycles." Chemistry & Biodiversity 5, no. 6 (June 2008): 1204–12. http://dx.doi.org/10.1002/cbdv.200890097.
Full textMartin, Anthony R., Anthony Chartoire, Alexandra M. Z. Slawin, and Steven P. Nolan. "Extending the utility of [Pd(NHC)(cinnamyl)Cl] precatalysts: Direct arylation of heterocycles." Beilstein Journal of Organic Chemistry 8 (September 27, 2012): 1637–43. http://dx.doi.org/10.3762/bjoc.8.187.
Full textBąchor, Urszula, and Marcin Mączyński. "Selected β2-, β3- and β2,3-Amino Acid Heterocyclic Derivatives and Their Biological Perspective." Molecules 26, no. 2 (January 15, 2021): 438. http://dx.doi.org/10.3390/molecules26020438.
Full textSachar, Anand, Poonam Gupta, Shallu Gupta, and R. L. Sharma. "A novel approach towards the synthesis of tricyclic systems based on pyridine, pyran, thiopyran, azepine, oxepin, thiepin, and pyrimidine rings under different solvent conditions." Canadian Journal of Chemistry 88, no. 5 (May 2010): 478–84. http://dx.doi.org/10.1139/v10-015.
Full textRomański, Jarosaw, Grzegorz Mlostoń, and Sylwia Szynkiewicz. "Straightforward Access to New Cage-Functionalized Sulfur Heterocycles." Synthesis, no. 14 (2003): 2259–64. http://dx.doi.org/10.1055/s-2003-41444.
Full textXu, Ping, Bo Yu, Fu Li Li, Xiao Feng Cai, and Cui Qing Ma. "Microbial degradation of sulfur, nitrogen and oxygen heterocycles." Trends in Microbiology 14, no. 9 (September 2006): 398–405. http://dx.doi.org/10.1016/j.tim.2006.07.002.
Full textZayed, Salem E., and Ibrahim A. Hussin. "KETOKETEN gem-DITHIOLS: SYNTHESIS OF SEVERAL SULFUR HETEROCYCLES." Phosphorus, Sulfur, and Silicon and the Related Elements 84, no. 1-4 (November 1, 1993): 191–96. http://dx.doi.org/10.1080/10426509308034331.
Full textFabian, Jürgen, and B. Andes Hess. "λ4σ2-Sulfur Heterocycles. Anab Initioand Density Functional Study." Journal of Organic Chemistry 62, no. 6 (March 1997): 1766–74. http://dx.doi.org/10.1021/jo961776e.
Full textZoller, Uri. "In Pursuit of Stable, Strained Smallring Sulfur Heterocycles." Sulfur reports 20, no. 2 (December 1997): 173–95. http://dx.doi.org/10.1080/01961779708047919.
Full textForeman, Mark R. StJ, Alexandra M. Z. Slawin, and J. Derek Woollins. "Phosphorus–sulfur–nitrogen heterocycles from diferrocenyl dithiadiphosphetane disulfide." Chemical Communications, no. 14 (1997): 1269–70. http://dx.doi.org/10.1039/a702857a.
Full textMartins, Andrew, and Mark Lautens. "A Palladium-Catalyzed Approach to Polycyclic Sulfur Heterocycles." Journal of Organic Chemistry 73, no. 22 (November 21, 2008): 8705–10. http://dx.doi.org/10.1021/jo8020105.
Full textNolte, Thies, and Jan T. Andersson. "Capillary electrophoretic separation of polycyclic aromatic sulfur heterocycles." Analytical and Bioanalytical Chemistry 395, no. 6 (August 24, 2009): 1843–52. http://dx.doi.org/10.1007/s00216-009-3034-z.
Full textAbdel-Wahab, Bakr F., Saad Shaaban, and Gamal A. El-Hiti. "Synthesis of sulfur-containing heterocycles via ring enlargement." Molecular Diversity 22, no. 2 (January 31, 2018): 517–42. http://dx.doi.org/10.1007/s11030-017-9810-3.
Full textMajumdar, Krishna C., and Anwesha Bandyopadhyay. "Synthesis of Sulfur Heterocycles by Thio- Claisen Rearrangement." Monatshefte f�r Chemie / Chemical Monthly 135, no. 5 (May 1, 2004): 581–87. http://dx.doi.org/10.1007/s00706-003-0109-y.
Full textDočekal, Vojtěch, Bedřich Formánek, Ivana Císařová, and Jan Veselý. "Correction: A formal [4 + 2] cycloaddition of sulfur-containing alkylidene heterocycles with allenic compounds." Organic Chemistry Frontiers 6, no. 22 (2019): 3810. http://dx.doi.org/10.1039/c9qo90096a.
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