Relevant bibliographies by topics / Synthorus

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  2. Dissertations / Theses
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Academic literature on the topic 'Synthorus'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Synthorus"

1

Saha, Subhankar, Somnath Ganguly, and Gautam R. Desiraju. "Graded IR Filters: Distinguishing Between Single and Multipoint NO2···I Halogen Bonded Supramolecular Synthons (P, Q, and R Synthons)." Australian Journal of Chemistry 67, no. 12 (2014): 1840. http://dx.doi.org/10.1071/ch14361.

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The NO2···I supramolecular synthon is a halogen bonded recognition pattern that is present in the crystal structures of many compounds that contain these functional groups. These synthons have been previously distinguished as P, Q, and R types using topological and geometrical criteria. A five step IR spectroscopic sequence is proposed here to distinguish between these synthon types in solid samples. Sets of known compounds that contain the P, Q, and R synthons are first taken to develop IR spectroscopic identifiers for them. The identifiers are then used to create graded IR filters that sieve
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Saha, Subhankar, Lalit Rajput, Sumy Joseph, Manish Kumar Mishra, Somnath Ganguly, and Gautam R. Desiraju. "IR spectroscopy as a probe for C–H⋯X hydrogen bonded supramolecular synthons." CrystEngComm 17, no. 6 (2015): 1273–90. http://dx.doi.org/10.1039/c4ce02034k.

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Koča, Jaroslav. "A mathematical model of the synthon." Collection of Czechoslovak Chemical Communications 53, no. 5 (1988): 1007–17. http://dx.doi.org/10.1135/cccc19881007.

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A mathematical model of the synthon is suggested. The term synthon is used to denote one or several molecules or their part(s) with free valences. The notion of isomeric synthons on a set of atoms A and that of the Family of Isomeric Synthons FIS(A) are introduced. Matrix operators are defined for modelling the elementary steps of reorganization of electrons during reactions. A new notion of the reaction distance of isomeric synthons is introduced as the smallest number of elementary steps of reorganization of electrons during the reaction transforming one synthon into another.
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Torubaev, Yury V. "Chimeric supramolecular synthons in Ph2Te2(I2)Se." Acta Crystallographica Section C Structural Chemistry 76, no. 6 (2020): 579–84. http://dx.doi.org/10.1107/s2053229620006166.

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Iodination of Ph2Te2Se by molecular iodine is directed towards the Te atom and yields {diiodo[(phenyltellanyl)selanyl]-λ4-tellanyl}benzene, PhTeSeTeI2Ph or C12H10I2SeTe2. The molecule can be considered as a chimera of PhTeSeR, PhTeSeTePh and R′TeI2Ph fragments. The crystal structure features a complex interplay of the supramolecular synthons Te...π(Ph), Se...Te and I...Te, combining molecules into a three-dimensional framework. Their combination affords long-range supramolecular synthons which are fused in a way resembling the mythological chimera and could be defined as chimeric supramolecula
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Bolla, Geetha, and Ashwini Nangia. "Supramolecular synthon hierarchy in sulfonamide cocrystals with syn-amides and N-oxides." IUCrJ 6, no. 4 (2019): 751–60. http://dx.doi.org/10.1107/s2052252519005037.

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Sulfonamide drugs are well known antibacterial and antimicrobial molecules for pharmaceutical development. Building a library of suitable supramolecular synthons for the sulfonamide functional group and understanding their crystal structures with partner coformer molecules continues to be a challenge in crystal engineering. Although a few sulfonamide cocrystals with amides and N-oxides have been reported, the body of work on sulfonamide synthons is limited compared with those that have carboxylic acids and carboxamides. To address this structural gap, the present work is primarily focused on s
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Mendoza-Meroño, Rafael, and Santiago García-Granda. "(1E,2E)-2-Methyl-3-phenylacrylaldehyde thiosemicarbazone." Acta Crystallographica Section E Structure Reports Online 68, no. 6 (2012): o1840. http://dx.doi.org/10.1107/s1600536812022386.

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In the crystal structure of the title compound, C11H13N3S, molecules form centrosymmetric synthons with an R 2 2(8) graph-set motif, linked by pairs of N—H...S hydrogen bonds. The synthons are connected through further N—H...S hydrogen bonds, extending the packing to form a two-dimensional network lying parallel to (001). In addition, C—H...π interactions are observed.
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Cai, Linhong, Lan Jiang, Cong Li, Xiaoshu Guan, Li Zhang, and Xiangnan Hu. "Multicomponent Crystal of Metformin and Barbital: Design, Crystal Structure Analysis and Characterization." Molecules 26, no. 14 (2021): 4377. http://dx.doi.org/10.3390/molecules26144377.

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The formation of most multicomponent crystals relies on the interaction of hydrogen bonds between the components, so rational crystal design based on the expected hydrogen-bonded supramolecular synthons was employed to establish supramolecular compounds with desirable properties. This theory was put into practice for metformin to participate in more therapeutic fields to search for a fast and simple approach for the screening of candidate crystal co-formers. The prediction of intermolecular synthons facilitated the successful synthesis of a new multicomponent crystal of metformin (Met) and bar
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Koval', I. V. "Thiols as synthons." Russian Chemical Reviews 62, no. 8 (1993): 769–86. http://dx.doi.org/10.1070/rc1993v062n08abeh000046.

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Vidal-Albalat, A., K. Świderek, J. Izquierdo, S. Rodríguez, V. Moliner, and F. V. González. "Catalytic enantioselective epoxidation of nitroalkenes." Chemical Communications 52, no. 65 (2016): 10060–63. http://dx.doi.org/10.1039/c6cc03539f.

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Bharadwaj, Parimal K. "Metal ion binding by laterally non-symmetric macrobicyclic oxa–aza cryptands." Dalton Transactions 46, no. 18 (2017): 5742–75. http://dx.doi.org/10.1039/c7dt00722a.

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Dissertations / Theses on the topic "Synthorus"

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Fisher, D. "Synthons for isobutylamides." Thesis, University of Nottingham, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.353545.

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Ocando, Mavarez Edgar. "Phosphonitriles, nouveaux synthons en chimie hétérocyclique." Grenoble 2 : ANRT, 1988. http://catalogue.bnf.fr/ark:/12148/cb37617146v.

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Ocando, Mavarez Edgar. "Phosphonitriles, nouveaux synthons en chimie heterocyclique." Toulouse 3, 1988. http://www.theses.fr/1988TOU30069.

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Cox, Philip Brian. "Novel chemo-enzymatic approaches to natural and unnatural product synthesis." Thesis, University of Exeter, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.277096.

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Lapouge, Pahlawan Sophie. "Synthèse et réactivité de nouveaux synthons imidazoliques." Aix-Marseille 3, 1997. http://www.theses.fr/1997AIX30124.

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Ce travail est consacre d'une part, a l'etude de deux reactions nouvelles decouvertes au laboratoire de chimie moleculaire organique : - synthese du 1,2-dimethyl-4-(1,1,2-trimethyl-2-nitropropyl) imidazole a partir du 1,2-dimethyl-5-nitroimidazole (dimetridazole, emtryl) et du 2-nitropropane en exces en milieu basique faisant intervenir une reaction de cine-substitution suivie d'une reaction de transfert monoelectronique (s#r#n1). - hydrolyse du 1,2-dimethyl-4-(1,1,2-trimethyl-2-nitropropyl)imidazole au reflux de l'eau en alcool tertiaire correspondant, et d'autre part, a la valorisation chimi
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Dussenne, Corentin. "Nouveaux synthons verts par anhydrisation de polyols." Thesis, Lille 1, 2017. http://www.theses.fr/2017LIL10131.

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La prise de conscience de l’enjeu environnemental est en train de transformer notre conception de la chimie, la faisant évoluer vers une chimie moderne portée par des concepts novateurs de chimie durable et plus respectueuse de l’environnement. Parmi ces concepts, la substitution à terme de la matière première pétrosourcée par la biomasse constitue actuellement avec le développement de procédés catalytiques, un des enjeux majeurs de la chimie verte. L’isosorbide est une molécule phare de cette nouvelle chimie, provenant de la filière sucre, ce diol est obtenu par anhydrisation du sorbitol lui-
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Schauer, Philip A. "Organometallic synthons for highly conjugated redox-active materials." University of Western Australia. School of Biomedical, Biomolecular and Chemical Sciences, 2009. http://theses.library.uwa.edu.au/adt-WU2009.0166.

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[Truncated abstract] This thesis describes various synthetic approaches toward the synthesis of highly conjugated complexes incorporating multiple transition metal centres. Particular attention is given to the synthesis of mononuclear complexes that allow for the facile assembly of discrete oligo- and poly-nuclear complexes in a controlled, stepwise fashion. Conjugated multi-metallic materials are of interest on account of their unique photophysical and electronic properties, with a particular emphasis on elucidating the nature of intramolecular communication between multiple metal centres. Ch
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Ellenberger, William Paul. "Synthesis of DEF ring synthons to nogarol anthracyclines /." Full text open access at:, 1987. http://content.ohsu.edu/u?/etd,136.

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McGlone, Thomas. "Engineering functional nano-architectures utilising polyoxometalate based synthons." Thesis, University of Glasgow, 2011. http://theses.gla.ac.uk/2390/.

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The host-guest chemistry of the isopolyoxometalate {W36} crown-like cluster is investigated. Previous reports showed that the cluster can specifically bind primary amines via a central binding pocket formed by six terminal oxo ligands on the all - inorganic, cation binding host. This assembly strategy was transformed to utilise the incorporation of long chain alkyl diammonium guest cations to physically define the supramolecular structure of the clusters with respect to each other and demonstrate the structure direction as a function of alkyl chain length. The systematic variation of chain len
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Jacques, Frédéric. "Préparation de synthons chiraux par réactions enzymatiques énantiosélectives." Thesis, Université Laval, 2009. http://www.theses.ulaval.ca/2009/26268/26268.pdf.

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Books on the topic "Synthorus"

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Soloshonok, Vadim A., ed. Fluorine-Containing Synthons. American Chemical Society, 2005. http://dx.doi.org/10.1021/bk-2005-0911.

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Witczak, Zbigniew J., and Kuniaki Tatsuta, eds. Carbohydrate Synthons in Natural Products Chemistry. American Chemical Society, 2002. http://dx.doi.org/10.1021/bk-2003-0841.

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Ouali, Dehimi. Enantioselective synthesis of novel Corynanthe indole alkaloid synthons. University of Salford, 1991.

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Bennett, Lisa Ruth. Enantioselective synthetic approaches tp natural products based on functionalised CIS-bicyclo[3.3.0]octane synthons. University of Salford, 1995.

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Soloshonok, Vadim A. Fluorine-Containing Synthons. An American Chemical Society Publication, 2005.

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A, Soloshonok V., American Chemical Society. Division of Fluorine Chemistry, American Chemical Society. Division of Medicinal Chemistry, and American Chemical Society. Division of Organic Chemistry, eds. Fluorine-containing synthons. American Chemical Society, 2005.

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7

Organofluorine Chemistry: Techniques and Synthons (Topics in Current Chemistry). Springer, 1997.

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Advances in the Use of Synthons in Organic Chemistry. Elsevier, 1993. http://dx.doi.org/10.1016/c2013-0-01304-7.

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Dondoni, Allessandro. Advances in the Use of Synthons in Organic Chemistry: A Research Annual (Advances in the Use of Synthons in Organic Chemistry). Jai Pr, 1993.

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Penta, Santhosh. Dehydroacetic Acid and Its Derivatives: Useful Synthons in Organic Synthesis. Elsevier Science & Technology Books, 2017.

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Book chapters on the topic "Synthorus"

1

Müller, Robert K. "Polyene Synthons." In Carotenoids. Birkhäuser Basel, 1996. http://dx.doi.org/10.1007/978-3-0348-9323-7_8.

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Lundt, Inge. "Aldonolactones as chiral synthons." In Glycoscience Synthesis of Substrate Analogs and Mimetics. Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/bfb0119255.

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Bickelhaupt, F. "Metallacyclobutanes: Synthons and Catalysts." In Organometallics in Organic Synthesis 2. Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-74269-9_9.

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Taylor, Stephen C. "Chiral Synthons by Biocatalysis." In Biocatalysis. Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-010-9124-4_7.

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Koča, J., M. Kratochvíl, L. Matyska, V. Kvasnička, and J. Pospíchal. "S-Graphs and Synthons." In Lecture Notes in Chemistry. Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-93416-2_3.

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Šunjić, Vitomir, and Vesna Petrović Peroković. "Disconnection, Synthons, Introductory Example." In Organic Chemistry from Retrosynthesis to Asymmetric Synthesis. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-29926-6_1.

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Sato, Tsuneo, Junzo Otera, and Hitosi Nozaki. "Carbene Synthons in Monothioacetal Reactions." In Advances in Metal Carbene Chemistry. Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-2317-1_42.

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Nangia, Ashwini, and Gautam R. Desiraju. "Supramolecular Synthons and Pattern Recognition." In Topics in Current Chemistry. Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/3-540-69178-2_2.

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Li, Ying, Anne-Sylvie Fabiano-Tixier, and Farid Chemat. "Essential Oils as Synthons for Green Chemistry." In SpringerBriefs in Molecular Science. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-08449-7_7.

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Simon, Helmut. "Chiral Synthons by New Oxidoreductases and Methodologies." In Biocatalysis. Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-010-9124-4_11.

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Conference papers on the topic "Synthorus"

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Morin-Allory, Katell, Fatemeh Negin Javaheri, and Dominique Borrione. "SyntHorus-2: Automatic prototyping from PSL." In 2013 IFIP/IEEE 21st International Conference on Very Large Scale Integration (VLSI-SoC). IEEE, 2013. http://dx.doi.org/10.1109/vlsi-soc.2013.6673253.

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Oddos, Yann, Katell Morin-Allory, and Dominique Borrione. "SyntHorus: Highly efficient automatic synthesis from PSL to HDL." In 2009 17th IFIP International Conference on Very Large Scale Integration (VLSI-SoC). IEEE, 2009. http://dx.doi.org/10.1109/vlsisoc.2009.6041335.

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Ruiz, Hérica Elaine Barbosa, Cris Ellen Zampier, and Carlos Henrique Santos. "ALUNOS DE EDUCAÇÃO ESPECIAL APRESENTAM SYNTHOMAS DE POESIA." In Congresso Brasileiro de Educação Especial. Galoa, 2014. http://dx.doi.org/10.17648/galoa-cbee-6-28484.

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Khan, Mohd Shahnawaz, Saba Parveen Siddiqui, and Daya Seth. "Reactive methylene compounds as synthons for various bio active molecules." In The 19th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2015. http://dx.doi.org/10.3390/ecsoc-19-a050.

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Roy, Vincent, Ugo Pradere, Aurélien Montagu, Steven P. Nolan, and Luigi A. Agrofoglio. "Phosphonate synthons bearing biolabile group for olefin cross metathesis synthesis of acyclonucleoside phosphonate analogs." In XVth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2011. http://dx.doi.org/10.1135/css201112213.

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Rusinov, V., V. Charushin та О. Chupakhina. "NITRO SYNTHONS IN THE SYNTHESIS OF NITRO DERIVATIVES OF AZOLO[1,5-а]PYRIMIDINES AND AZOLO[5,1-с]-1,2,4-TRIAZINES". У Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m720.aks-2019/47-52.

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Lee, Jinq-Chyi, Shankar R. Thopate, Fa-Chen Chi, Shu-Wen Chang, Cheng-Chung Wang, and Shang-Cheng Hung. "1,6-ANHYDRO-BETA-L-HEXOPYRANOSES AS P0TENT SYNTHONS IN THE SYNTHESIS OF THE DISACCHARIDE UNITS OF BLEOMYCIN A2 AND HEPARIN." In XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.590.

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Bilokin, Yaroslav, Sergey Kovalenko, Maxim Vasilyef, Igor Bylov, and Konstantin Sytnik. "2-Imino-2H-1-benzopyrans as Versatile Synthons in Heterocyclic Synthesis: Studies on Novel Rearrangements of 3-Substituted 2-Imino-2H-1- benzopyrans Under Action of N-Nucleophiles." In The 2nd International Electronic Conference on Synthetic Organic Chemistry. MDPI, 1998. http://dx.doi.org/10.3390/ecsoc-2-01676.

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