Relevant bibliographies by topics / Succinimidyl

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Succinimidyl'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Succinimidyl"

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Leonard, Nicholas M., and Jarmila Brunckova. "In Situ Formation ofN-Trifluoroacetoxy Succinimide (TFA-NHS): One-Pot Formation of Succinimidyl Esters,N-Trifluoroacetyl Amino Acid Succinimidyl Esters, andN-Maleoyl Amino Acid Succinimidyl Esters." Journal of Organic Chemistry 76, no. 21 (2011): 9169–74. http://dx.doi.org/10.1021/jo201686e.

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Merényi, Gábor, Johan Lind, Lennart Eberson, et al. "The Return of the Succinimidyl Radical." Acta Chemica Scandinavica 52 (1998): 62–66. http://dx.doi.org/10.3891/acta.chem.scand.52-0062.

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Mamat, Constantin, Daniel Holger Weiß, and Martin Köckerling. "X-ray Structures of Succinimidyl Halobenzoates." Crystals 7, no. 3 (2017): 90. http://dx.doi.org/10.3390/cryst7030090.

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Mujumdar, Swati R., Ratnakar B. Mujumdar, Charsetta M. Grant, and Alan S. Waggoner. "Cyanine-Labeling Reagents: Sulfobenzindocyanine Succinimidyl Esters." Bioconjugate Chemistry 7, no. 3 (1996): 356–62. http://dx.doi.org/10.1021/bc960021b.

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Janabi, Mustafa, Catherine M. Pollock, Ann-Marie Chacko, and Duncan H. Hunter. "Resin-supported arylstannanes as precursors for radiolabeling with iodine: benzaldehydes, benzoic acids, benzamides, and NHS esters." Canadian Journal of Chemistry 93, no. 2 (2015): 207–17. http://dx.doi.org/10.1139/cjc-2014-0265.

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A highly cross-linked polystyrene resin bearing a reactive chlorostannane moiety 1 has been used to generate a variety of arylstannane radiopharmaceutical precursors for no-carrier-added radioiodination. The resins were characterized for their solvent compatibility and sensitivity to acid cleavage. Resin-supported arylstannanes synthesized via their aryllithium analogues include 3- and 4-stannylbenzaldehydes, 3- and 4-stannylbenzoic acids, and 3- and 4-N-succinimidyl benzoates. A three-step route to the resin-supported stannylbenzoic acids 12a/b was developed through resin-supported benzaldehy
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MRIDULA, VERMA, and M. VERMA SHIVA. "Hydrogen Bonding and the Stereochemistry of Hydrazones and Hydrazides derived from 1,3-Dicarbonyl Compounds involving Imino Nitrogen." Journal of Indian Chemical Society Vol. 69, Sep 1992 (1992): 561–62. https://doi.org/10.5281/zenodo.6006453.

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Department of Chemistry, Banaras Hindu University, Varanasi-221 005 <em>Manuscript received 5 August 1991, revised 8 June 1992, accepted 3 July 1992</em> <em>&beta;</em>-Diketones form hydrazones with <em>N&#39; ,N&#39;</em> -diacylhydrazines and exhibit a six-membered hydrogen bonded cyclic ketiminyl system involving the imino nitrogen. <sup>1</sup>H nmr spectra of the hydrazones obtained from <em>N</em>-amino -&alpha;, &beta;- (9,10-dihydroanthracene-9,10-endo-diyl)succinimide and acetylacetone demonstrated restricted rotation about <em>N-N</em> bond and a planer hydrogen bonded cyclic syste
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Mujumdar, Ratnakar B., Lauren A. Ernst, Swati R. Mujumdar, Christopher J. Lewis, and Alan S. Waggoner. "Cyanine dye labeling reagents: Sulfoindocyanine succinimidyl esters." Bioconjugate Chemistry 4, no. 2 (1993): 105–11. http://dx.doi.org/10.1021/bc00020a001.

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Bardajee, Ghasem Rezanejade, Mitchell A. Winnik, and Alan J. Lough. "Succinimidyl 7-methoxy-2H-chromene-3-carboxylate." Acta Crystallographica Section E Structure Reports Online 63, no. 3 (2007): o1513—o1514. http://dx.doi.org/10.1107/s1600536807004175.

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In the title molecule, C15H11NO7, the dihedral angle between the coumarin unit and the succinimide unit is 72.36 (4)°. The crystal structure is stabilized by weak intermolecular C—H...O hydrogen bonds and π–π stacking interactions.
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van den Boom, Johannes, Marija Mamić, Daniele Baccelliere, et al. "Peptidyl Succinimidyl Peptides as Taspase 1 Inhibitors." ChemBioChem 15, no. 15 (2014): 2233–37. http://dx.doi.org/10.1002/cbic.201402108.

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Southwick, Philip L., Lauren A. Ernst, Erica W. Tauriello, et al. "Cyanine dye labeling reagents—carboxymethylindocyanine succinimidyl esters." Cytometry 11, no. 3 (1990): 418–30. http://dx.doi.org/10.1002/cyto.990110313.

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Dissertations / Theses on the topic "Succinimidyl"

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Husain, Philip Anwar. "Investigative enzymology of selected monooxygenases and development of (S)-N-Succinimidyl-a-Methoxyphenylacetate as a novel tool for assignment of absolute configuration." Diss., Georgia Institute of Technology, 1992. http://hdl.handle.net/1853/27579.

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Hoppmann, Susan. "18F-markierte S100-Proteine als potentielle Radioliganden für die funktionelle Charakterisierung des Rezeptors für advanced glycation endproducts (RAGE) in vitro und in vivo." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2009. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-24725.

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Die Interaktion von S100-Proteinen mit dem Rezeptor für advanced glycation endproducts (RAGE) wird als hoch relevant bei der Entstehung, Manifestation und Progression verschiedener entzündlicher Erkrankungen sowie bei der Tumorigenese gewertet. Das tiefergehende Verständnis der Interaktion von S100-Proteinen mit RAGE in vivo stellt eine wissenschaftliche Herausforderung dar und ist ein Ansatz für therapeutische Interventionen. Darüber hinaus stellen Untersuchungen zum Metabolismus von extrazellulär zirkulierenden S100-Proteinen in vivo einen vielversprechenden Forschungsansatz zur Analyse von
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Cunha, Saulo Marques da. "Síntese de análogos succinimidas da (-)-julocrotina." reponame:Repositório Institucional da UnB, 2013. http://repositorio.unb.br/handle/10482/15084.

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Dissertação (mestrado)—Universidade de Brasília, Instituto de Química, Programa de Pós-Graduação em Química, 2013.<br>Submitted by Alaíde Gonçalves dos Santos (alaide@unb.br) on 2013-11-13T14:03:47Z No. of bitstreams: 1 2013_SauloMarquesdaCunha.pdf: 5424545 bytes, checksum: 70f8ae81d705e8d41b709943a346aa31 (MD5)<br>Approved for entry into archive by Guimaraes Jacqueline(jacqueline.guimaraes@bce.unb.br) on 2014-02-03T12:20:23Z (GMT) No. of bitstreams: 1 2013_SauloMarquesdaCunha.pdf: 5424545 bytes, checksum: 70f8ae81d705e8d41b709943a346aa31 (MD5)<br>Made available in DSpace on 2014-02-03T12:20:2
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Wei, Lai. "Asymmetric organocatalysis in the Michael reaction of cyclic α-alkyl ketones : enantioselective synthesis of suberosanes and succinimides". Thesis, Université Paris-Saclay (ComUE), 2018. http://www.theses.fr/2018SACLS325.

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La découverte des activités cytotoxiques impressionnantes des subérosanes, des sesquiterpènes d’origine marine isolées dès 1996 de la gorgone Subergorgia suberosa, ainsi que leurs structures tricycliques complexes possédant jusqu’à cinq centre stéréogènes contigus dont un centre quaternaire central, ont fait de ces molécules des cibles de choix tant pour les acteurs de la chimie médicinale que pour ceux travaillant dans le domaine de la synthèse totale. Enfin, une molécule d’origine synthétique « simplifiée » de cette famille, la nor-subérosénone, a également montré des activités cytotoxiques
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Lenz, Stefan [Verfasser], and Armin [Akademischer Betreuer] Geyer. "Succinimid-Thioether in der Peptidligation - Methodenentwicklung und Strukturaufklärung / Stefan Lenz ; Betreuer: Armin Geyer." Marburg : Philipps-Universität Marburg, 2018. http://d-nb.info/1164156217/34.

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Sutton, Michael Robert. "Investigation of succinimide dispersants and their interactions using reduced total oil volume lubricant degradation." Thesis, De Montfort University, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.391994.

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Wong, Shi Quan. "Using Caenorhabditis elegans to identify succinimide-based neuroprotective compounds and their mechanisms of action." Thesis, University of Liverpool, 2017. http://livrepository.liverpool.ac.uk/3017944/.

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Zhang, Jie. "Influence of succinimide dispersants on film formation, friction and antiwear properties of zinc dialkyl dithiophosphate." Thesis, Imperial College London, 2012. http://hdl.handle.net/10044/1/9196.

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ZDDP (zinc dialkyldithiophosphate) is arguably the most successful antiwear additive ever employed in crankcase engine lubricants. It was originally used as an antioxidant and shortly afterwards recognized for its antiwear and extreme pressure properties. Unfortunately, another critical additive polyisobutylsuccinimide-polyamine (PIBSA-PAM), which is used as a dispersant in engine oils, is known to be antagonistic to ZDDP in terms of film formation, friction and wear. The mechanisms of this antagonism have been widely studied, but they are still not well understood. Furthermore, in order to pr
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Silva, Fabio Machado da. "Reações entre ácidos β-cianocarboxílicos e nitrogênios nucleofílicos: uma eficiente estratégia para a síntese de succinimidas, pirrolidinonas e tetrazóis". Universidade Federal de Santa Maria, 2011. http://repositorio.ufsm.br/handle/1/4204.

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Conselho Nacional de Desenvolvimento Científico e Tecnológico<br>This work presents the synthesis of 41 succinimides, 24 pyrrolidinones and 8 tetrazoles, all presenting unprecedented chemical structure, except for the succinimide 3-ethoxy-1-methylpyrrolidine-2,5-dione. These compounds were synthesized by cyclization reactions of β-cyanocarboxylic acids of general formula HO2CCH(R1)CH(OR)CN, where R/R1 = Et/H (9), -(CH2)2- (10), -(CH2)3- (11), Et/Me (12), i-Pr/H (13), s-Bu/H (14), i-Pr/Me (15), s-Bu/Me (16), with amine derivatives or sodium azide. Initially NR2-substituted 3-ethoxypyrrolidine
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Flores, Ferrándiz Jesús. "Chiral Aminocarbamates Derived from trans-Cyclohexane-1,2-Diamines as Organocatalysts in Conjugate Addition Reactions." Doctoral thesis, Universidad de Alicante, 2017. http://hdl.handle.net/10045/73589.

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The thesis has been divided in two chapters: Chapter I describes the preparation of primary-amine monocarbamates from enantiopure trans-cyclohexane-1,2-diamines and their use as chiral organocatalysts in the enantioselective Michael addition reaction of aldehydes and ketones to maleimides, to synthesize enantiomerically enriched substituted succinimides. In the conjugate addition reaction of aldehydes to maleimides in conventional volatile organic solvents, it has been found that these organocatalysts are able to generate both enantiomers of the corresponding succinimide using only one enantio
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Books on the topic "Succinimidyl"

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DeSantis, Grace. Inhibition of [alpha]-chymotrypsin and subtilisin Carlsberg by N-oxamide, [alpha]-keto amide and N-succinimidyl derivatives. National Library of Canada, 1996.

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Zerizer, Hafiza. Synthesis and photochemistry of B-amino-ketones and A-substituted succinimides. University of Salford, 1985.

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Sutton, Michael Robert. Investigation of succinimide dispersants and their interactions using reduced total oil volume lubricant degradation. De Montfort University, 2000.

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Stanik, Winicjusz. Investigation into the performance characteristics polyisobutenyl succinimides as detergent-dispersant additive to motor fuel. Instytut Nafty i Gazu - Państwowy Instytut Badawczy, 2015. http://dx.doi.org/10.18668/pn2015.206.

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Book chapters on the topic "Succinimidyl"

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Zalipsky, Samuel, Robert Seltzer, and Kwang Nho. "Succinimidyl Carbonates of Polyethylene Glycol." In ACS Symposium Series. American Chemical Society, 1991. http://dx.doi.org/10.1021/bk-1991-0469.ch010.

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Shao, Xia. "Synthesis ofN-Succinimidyl 4-[18F]Fluorobenzoate ([18F]SFB)." In Radiochemical Syntheses. John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118140345.ch9.

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Azari, Hassan, Loic P. Deleyrolle, and Brent A. Reynolds. "Using Carboxy Fluorescein Succinimidyl Ester (CFSE) to Identify Quiescent Glioblastoma Stem-Like Cells." In Cellular Quiescence. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7371-2_4.

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Strack, Guinevere, Robert Nichols, Plamen Atanassov, Heather R. Luckarift, and Glenn R. Johnson. "Modification of Carbon Nanotube Electrodes with 1-Pyrenebutanoic Acid, Succinimidyl Ester for Enhanced Bioelectrocatalysis." In Methods in Molecular Biology. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-550-7_14.

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Teschendorf, H. J., and R. Kretzschmar. "Succinimides." In Antiepileptic Drugs. Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-69518-6_19.

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Benoiton, N. L., Y. C. Lee, and F. M. F. Chen. "A new coupling method allowing epimerization-free aminolysis of segments: Use of succinimidyl esters obtained through mixed anhydrides." In Peptides 1994. Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-1468-4_84.

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Moskalenko, A. A., O. A. Toropygina, and Yu E. Erokhin. "Interaction of Hydrophilic Succinimidyl Ethers with Polypeptides of Pigment-Protein Complexes in Assembly A890 from Sulfur Photosynthetic Bacterium Chromatium Minutissimum." In Current Research in Photosynthesis. Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0511-5_241.

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Coort, Susan L. M., Jodil Willems, Will A. Coumans, et al. "Sulfo-N-succinimidyl esters of long chain fatty acids specifically inhibit fatty acid translocase (FAT/CD36)-mediated cellular fatty acid uptake." In Cellular Lipid Binding Proteins. Springer US, 2002. http://dx.doi.org/10.1007/978-1-4419-9270-3_27.

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Rankin, G. O., D. J. Yang, V. J. Teets, H. C. Shih, and P. I. Brown. "Role of Biotransformation in Acute N-(3,5-Dichlorophenyl)Succinimide-Induced Nephrotoxicity." In Nephrotoxicity. Springer US, 1989. http://dx.doi.org/10.1007/978-1-4757-2040-2_92.

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Papke, B. L. "Irreversible Adsorption of Poly(isobutenyl)-succinimide Dispersants onto Calcium Alkylarylsulfonate Colloids." In Mixed Surfactant Systems. American Chemical Society, 1992. http://dx.doi.org/10.1021/bk-1992-0501.ch026.

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Conference papers on the topic "Succinimidyl"

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Chang, Ta-Chau, Chien-Chih Chiang, and Konan Peck. "Conformational Structures of Dye-Oligonucleotides Studied by Satellite Holes." In Biomedical Optical Spectroscopy and Diagnostics. Optica Publishing Group, 2006. http://dx.doi.org/10.1364/bosd.1996.dr5.

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The spectral features of satellite holes in nonphotochemical hole burned spectra provide a promising method to identify different conformational structures of chromophore-oligonucleotides. Different hole burned spectra are observed when a 4,4-difluoro-5-(4-phenyl-l,3-butadienyl)-4-bora-3a,4a-diaza-s-indacene-3-propionic acid, succinimidyl ester (BODIPY) molecule is chemically bound to oligonucleotides of different base compositions, implying that different conformational structures exist among them. The study of satellite holes reveals that the conformational structure of BODIPY-oligonucleotid
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Chang, Ta-Chau, Chien-Chih Chiang, and Shiow-Hwa Chou. "Temperature-Annealing-Cycling Hole Burning Spectroscopies of Dye and Dye-Oligonucleotide Doped in Polymer Films." In Spectral Hole-Burning and Related Spectroscopies: Science and Applications. Optica Publishing Group, 1994. http://dx.doi.org/10.1364/shbs.1994.wd16.

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We have measured the temperature-annealing-cycling hole spectra of 5-(and 6-) carboxy-X-rhodamine N-hydroxy succinimidyl ester (RhSE) and the RhSE molecule with binding to the oligonucleotide of ten bases of Guanine (RhSE-10G) doped in polyvinyl alcohol (PVOH) films, respectively. Figure 1 shows the temperature-annealing-cycling hole spectra of zero phonon hole (ZPH) of RhSE/PVOH and RhSE-10G/PVOH, which were taken after burning 5 and 10 mins with a flux of ~ 40 mW/cm2 at λB ~ 5812 Å, respectively. It is found that the holes are reduced by 40 % and 50 % in the annealing spectra at Ta ~ 18 K. H
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Jefferson, J. R., J. T. Harmon, and G. A. Jamieson. "ADP-BINDING SITES IN PLATELETS: CHARACTERIZATION BY PHOTOAFFINITY LABELING AND BINDING STUDIES WITH FIXED PLATELETS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644463.

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Attempts to photoaffinity label platelet ADP receptors with 2-azidoADP have not been successful possibly due to the absence of a spacer arm between the nucleotide and the photolabile group. We have synthesized a probe having a long spacer arm by coupling 2-(3-aminopropylthio)-ADP to succinimidyl 4-3H-azidobenzoate. Labeling competable by ADP could not demonstrated with intact platelets. With isolated platelet membranes, three bands (Mr 140,000, 110,000 and 46,000) were labeled that were not competed by ADP while three other bands (Mr 188,000, 92,000 and 51,000) were competable by 100 uM ADP.An
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Reid, Jacqueline, and Jim Barker. "Understanding Polyisobutylene Succinimides (PIBSI) and Internal Diesel Injector Deposits." In SAE/KSAE 2013 International Powertrains, Fuels & Lubricants Meeting. SAE International, 2013. http://dx.doi.org/10.4271/2013-01-2682.

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Sibiescu, Doina, Carmen Mîţă, Mihaela Vizitiu, and Andra Manuela Crudu. "New complexes of silver (I) with N-hydroxy-succinimide." In Advanced Topics in Optoelectronics, Microelectronics, and Nanotechnologies 2016, edited by Marian Vladescu, Razvan Tamas, and Ionica Cristea. SPIE, 2016. http://dx.doi.org/10.1117/12.2243370.

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Williams, Sivanjali, and A. Hernandez-Castillo. "CHARACTERIZING THE STRUCTURE OF SUCCINIMIDE WITH BROADBAND ROTATIONAL SPECTROSCOPY." In 2023 International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2023. http://dx.doi.org/10.15278/isms.2023.7119.

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Derelı, Ömer, Levent Ateş, and Yusuf Erdoğdu. "Theoretical calculations of electron paramagnetic resonance parameters of succinimide radical." In SolarPACES 2017: International Conference on Concentrating Solar Power and Chemical Energy Systems. Author(s), 2018. http://dx.doi.org/10.1063/1.5078896.

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Ivanova, Ludmila V., Ruslan S. Muminov, and Olga V. Primerova. "Influence of polyalkenyl succinimides on the stability of petroleum dispersed systems." In Third International Scientific and Practical Symposium on Materials Science and Technology (MST-III 2023), edited by Ramazon Abdullozoda and Shahriyor Sadullozoda. SPIE, 2024. http://dx.doi.org/10.1117/12.3016634.

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Ahmed, Neam Hazim, and Saad H. Sultan. "Indirect spectrophotometric determination of pyridoxine hydrochloride using N-bromo succinimide and methyl red dye." In FIFTH INTERNATIONAL CONFERENCE ON APPLIED SCIENCES: ICAS2023. AIP Publishing, 2024. http://dx.doi.org/10.1063/5.0211532.

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Jonkman, L., F. de Jong, P. Sant, and J. R. Barnes. "Relation Between Molecular Structure of Succinimide Dispersants and Dispersancy of Soot in a Carbon Black Dispersancy Test." In 4th International Pacific Conference on Automotive Engineering. SAE International, 1987. http://dx.doi.org/10.4271/871274.

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