Relevant bibliographies by topics / Diazabicyclo[3.2.1]octane

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

Academic literature on the topic 'Diazabicyclo[3.2.1]octane'

Author: Grafiati
Published: 4 June 2021
Last updated: 5 February 2022

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Journal articles on the topic "Diazabicyclo[3.2.1]octane"

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Liu, Xiangyuan, Yanli Yin та Zhiyong Jiang. "Photoredox-catalysed formal [3+2] cycloaddition of N-aryl α-amino acids with isoquinoline N-oxides". Chemical Communications 55, № 77 (2019): 11527–30. http://dx.doi.org/10.1039/c9cc06249a.

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This work realizes a new synthetic utility of N-aryl α-amino acids as a 1,2-synthon, a new strategy to achieve dearomatization of isoquinolines, and the synthesis of valuable diazabicyclo[3.2.1]octane-based compounds.
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Helliwell, Madeleine, Yun You, and John A. Joule. "The dipolar cycloaddition of methyl acrylate to 1,5,6-trimethyl-3-oxidopyrazinium." Acta Crystallographica Section E Structure Reports Online 62, no. 4 (2006): o1293—o1294. http://dx.doi.org/10.1107/s1600536806007501.

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5,6-Dimethylpyrazin-2-one reacts with iodomethane to give a quaternary salt, deprotonation of which liberates a 3-oxidopyrazinium which undergoes a 1,3-dipolar cycloaddition with methyl acrylate to form methyl 5,8-dimethyl-4-methylene-2-oxo-3,8-diazabicyclo[3.2.1]octane-6-exo-carboxylate, C11H16N2O3, as the major product.
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Paliulis, Osvaldas, Dan Peters, Linas Miknius, and Algirdas Šačkus. "IMPROVED SYNTHESIS OF 8-METHYL-3, 8-DIAZABICYCLO [3.2.1] OCTANE." Organic Preparations and Procedures International 39, no. 1 (2007): 86–90. http://dx.doi.org/10.1080/00304940709458585.

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Huang, Long Jiang, and Da Wei Teng. "An improved and scalable process for 3,8-diazabicyclo[3.2.1]octane analogues." Chinese Chemical Letters 22, no. 5 (2011): 523–26. http://dx.doi.org/10.1016/j.cclet.2010.11.030.

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Boehringer, Régis, Philippe Geoffroy, and Michel Miesch. "Base catalyzed synthesis of bicyclo[3.2.1]octane scaffolds." Organic & Biomolecular Chemistry 13, no. 25 (2015): 6940–43. http://dx.doi.org/10.1039/c5ob00933b.

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A base-catalyzed and time controlled reaction of 1,3-cyclopentanediones tethered to activated olefins afforded in high yields either bicyclo[3.2.1]octane-6,8-dione or bicyclo[3.2.1]octane-6-carboxylate derivatives.
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Shainyan, Bagrat A., Mikhail Yu Moskalik, Vera V. Astakhova, and Uwe Schilde. "Novel design of 3,8-diazabicyclo[3.2.1]octane framework in oxidative sulfonamidation of 1,5-hexadiene." Tetrahedron 70, no. 30 (2014): 4547–51. http://dx.doi.org/10.1016/j.tet.2014.04.095.

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Woo, Grace H. C., Se-Ho Kim та Peter Wipf. "π-Allyl palladium approach toward the diazabicyclo[3.2.1]octane core of the naphthyridinomycin alkaloids". Tetrahedron 62, № 45 (2006): 10507–17. http://dx.doi.org/10.1016/j.tet.2006.06.114.

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Fujiu, Motohiro, Katsuki Yokoo, Toshiaki Aoki та ін. "Synthesis of 2-Thio-Substituted 1,6-Diazabicyclo[3.2.1]octane Derivatives, Potent β-Lactamase Inhibitors". Journal of Organic Chemistry 85, № 15 (2020): 9650–60. http://dx.doi.org/10.1021/acs.joc.0c00980.

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Villa, S. "3,8-Diazabicyclo-[3.2.1]-octane derivatives as analogues of ambasilide, a Class III antiarrhythmic agent." European Journal of Medicinal Chemistry 36, no. 6 (2001): 495–506. http://dx.doi.org/10.1016/s0223-5234(01)01246-6.

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Shainyan, Bagrat A., Mikhail Yu Moskalik, Matthias Heydenreich, and Erich Kleinpeter. "Conformational equilibrium and dynamic behavior of bis-N -triflyl substituted 3,8-diazabicyclo[3.2.1]octane." Magnetic Resonance in Chemistry 52, no. 8 (2014): 448–52. http://dx.doi.org/10.1002/mrc.4086.

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Dissertations / Theses on the topic "Diazabicyclo[3.2.1]octane"

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Wang, Haiyu, та Abbas Shilabin. "Synthesis of 2-Carbamoyl-4-Oxo-1,5-Diazabicyclo [3.2.1] Octane Derivatives as a Possible Inhibitors of Serine β-Lactamases". Digital Commons @ East Tennessee State University, 2018. https://dc.etsu.edu/asrf/2018/schedule/178.

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Antibiotic resistance is becoming ever more severe due in part to the increasing use of antibiotic drugs. One significant contributor to this problem is the production of β-lactamase enzymes that provide resistance to common β-lactam antibiotics. The scope of this research is to synthesize and study the β-lactamase inhibitors of 2-carbamoyl-4-oxo-1,5-diazabicyclo [3.2.1] octane derivatives. Currently the research process is in the beginning stages of synthesizing three compounds: (R)-hexahydro-6-oxopyrimidine-4-carboxylic acid (1a), hexahydro-2,2-dimethyl-6-oxopyrimidine-4-carboxylic acid (1b)
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Spesyvtsev, R. "Experimental investigation of ultrafast internal conversion in aniline and 1,4-diazabicyclo[2.2.2]octane (DABCO)." Thesis, University College London (University of London), 2013. http://discovery.ucl.ac.uk/1384823/.

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Pump-probe time-resolved photoelectron spectroscopy is employed to investigate ultrafast non-adiabatic dynamics in aniline, deuterated aniline (aniline-D7) and 1,4- diazabicyclo[2.2.2]octane (DABCO). Aniline molecules are photoexcited over a wide range of wavelengths between 269 and 236 nm. Our observations reveal direct population of the S2(π3s/πσ∗) state. The photoelectron energy and angular distributions obtained in our experiments show an interesting bifurcation of the Rydberg population to two non-radiative decay channels. One of these involves ultrafast relaxation from the Rydberg compon
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Hazm, Jamal Eddine. "Silicates et aluminosilicates microporeux obtenus en milieu fluoré avec, comme structurants, le 1,4-diazabicyclo [2,2,2] octane (DABCO) ou le 1-azabicyclo [2,2,2] octane (quinuclidine)." Mulhouse, 1992. http://www.theses.fr/1992MULH0238.

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Ce travail s'inscrit dans le cadre de l'exploration d'une nouvelle voie de synthèse hydrothermale des zéolithes. L'ion mobilisateur hydroxyde habituellement utilisé est ici remplacé par l'ion fluorure, avec pour corollaire l'emploi de milieux de synthèse de pH typiquement compris entre environ 7 et 10. L'utilisation de 2 structurants organiques différents, le 1,4-diazabicyclo [2,2,2] octane (« DABCO » ou le 1-azabicyclo [2,2,2] octane (« quinuclidine ») - combiné à des rapports molaires Si/Al variables - a permis respectivement la préparation des zéolithes bêta et de type MTW d'une part, ainsi
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George, Nicolas. "Étude de la synthèse totale de tétrahydroisoquinoléines naturelles : quinocarcine, Tétrazomine et Lémonomycine. : rapide accés aux α-amidosulfures et leur utilisation en tant que précurseurs de N-acylimines dans la réaction de Friedel-Crafts". Phd thesis, Université Paris Sud - Paris XI, 2011. http://tel.archives-ouvertes.fr/tel-00980348.

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La quinocarcine, la tétrazomine et la lémonomycine constituent une sous-famille appartenant à la famille des tétrahydroisquinoléines trisubstituées naturelles. Ce sont des puissants agents cytotoxiques et possèdent de nombreuses activités biologiques telles qu'antitumorales et antibiotiques. Leur complexité structurale, leurs intérêts biologiques ainsi que leur faible rendement d'extraction du milieu naturel font de ces molécules des cibles attrayantes pour les chimistes de synthèse.Ces trois molécules sont constituées d'une tétrahydroisoquinoléine différemment substitué fusionnée avec un diaz
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Liron, Mélanie. "Synthèse totale de la quinocarcine." Phd thesis, Ecole Polytechnique X, 2006. http://pastel.archives-ouvertes.fr/pastel-00002175.

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La quinocarcine appartient à la famille des tétrahydroisoquinoléines, produits naturels qui constituent de puissants agents cytotoxiques et possèdent de nombreuses activités biologiques telles qu'antitumorales et antibiotiques. Son intérêt biologique ainsi qu'un faible rendement d'extraction du milieu naturel ont fait d'elle une cible attrayante en synthèse organique. Dans le but d'effectuer la synthèse totale de la quinocarcine, plusieurs stratégies ont été envisagées pour construire la structure tétracyclique ABCD. Ces stratégies se sont appuyées sur différentes étapes clé comme des réaction
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Wu, Chia-Yin, and 吳嘉吟. "Chemiluminescence of Luminol-Co(II)-NH2OH -1,4-Diazabicyclo[2,2,2]octane System and Its Analytical Applications." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/75930475333331563342.

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Book chapters on the topic "Diazabicyclo[3.2.1]octane"

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Ellenbroek, Bart, Alfonso Abizaid, Shimon Amir, et al. "Endo-3-(Diphenylmethoxy)-8-Methyl-8-Azabicyclo[3.2.1]Octane Methanesulfonate." In Encyclopedia of Psychopharmacology. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_4235.

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Morgan, Michael M., MacDonald J. Christie, Thomas Steckler, et al. "Methyl (1R,2R,3S,5S)-3-(Benzoyloxy)-8-Methyl-8-Azabicyclo[3.2.1] Octane-2-Carboxylate." In Encyclopedia of Psychopharmacology. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_3393.

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Bayri, B., G. Buntinx, O. Poizat, P. Valat, and V. Wintgens. "Combined Transient Absorption and Resonance Raman Studies of the Photoreduction of 2,2’-Bipyridine by 1,4-Diazabicyclo(2.2.2)octane (DABCO) in Acetonitrile." In Springer Proceedings in Physics. Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-84771-4_37.

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Ishioka, T., and I. Kanesaka. "Vibrational Study on Phase Transition Accompanied with an Abrupt Increase in Ionic Conductivity in N,N’-Distearyl-1,4-Diazabicyclo[2.2.2]Octane Dibromide." In Spectroscopy of Biological Molecules. Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0371-8_173.

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Zenkova, Marina, Natalia Beloglazova, Vladimir Sil'nikov, Valentin Vlassov, and Richard Giegé. "RNA Cleavage by 1,4-Diazabicyclo[2.2.2]octane–Imidazole Conjugates." In Methods in Enzymology. Elsevier, 2001. http://dx.doi.org/10.1016/s0076-6879(01)41171-2.

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Hatakeyama, S. "Using a Chiral Thiourea Activator with 1,4-Diazabicyclo[2.2.2]octane." In Lewis Base and Acid Catalysts. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-204-00342.

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Ashley, Eric, and Brian Stoltz. "A Dipolar Cycloaddition Strategy for the Synthesis of 3,8-Diazabicyclo[3.2.1]Octane Tetrahydroisoquinoline Antitumor Antibiotics: The Total Synthesis of (−)-Lemonomycin." In Strategies and Tactics in Organic Synthesis Volume 8. Elsevier, 2012. http://dx.doi.org/10.1016/b978-0-12-386540-3.00015-0.

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BLANKENSHIP, CRAIG, ANTHONY G. SOMMESE, LADDAWAN BORSUB, and SHELDON E. CREMER. "3-SILABICYLO[3.2.1]OCTANE AND ITS 3-GERMA AND 3-STANNA ANALOGUES." In Organometallic Syntheses. Elsevier, 1988. http://dx.doi.org/10.1016/b978-0-444-42956-8.50138-9.

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Hou, X. L., X. S. Peng, K. S. Yeung, and H. N. C. Wong. "1,4-Diazabicyclo[2.2.2]octane-Catalyzed Reaction of α-Halo Carbonyl Compounds with Dimethyl Acetylenedicarboxylate." In Fully Unsaturated Small-Ring Heterocycles and Monocyclic Five-Membered Hetarenes with One Heteroatom. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-109-00093.

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"Cocaine (3-benzoyloxy)-8methyl-8-azabicyclo[3.2.1]octane-2-carboxylic acid methyl ester)." In Encyclopedia of Genetics, Genomics, Proteomics and Informatics. Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6754-9_3242.

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Conference papers on the topic "Diazabicyclo[3.2.1]octane"

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Eggimann, Thomas, Nan Ibrahim, and Hal Wieser. "VCD Spectrum Of 6,8-Dioxabicyclo[3.2.1]Octane: Comparison Of Experimental And Model Spectra." In Intl Conf on Fourier and Computerized Infrared Spectroscopy, edited by David G. Cameron. SPIE, 1989. http://dx.doi.org/10.1117/12.969456.

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Valverde-Aguilar, Guadalupe, Jorge Garcia-Macedo, Xianghuai Wang, Jeffrey I. Zink, and Stephen F. Nelsen. "Photoinduced electron transfer in 2- tert -butyl-3-(anthracen-9-yl)-2,3-diazabicyclo[2.2.2]octane." In SPIE Optics + Photonics, edited by Zeno Gaburro and Stefano Cabrini. SPIE, 2006. http://dx.doi.org/10.1117/12.680904.

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Taher, Tarmizi, Lavini Indwi Saputri, Riza Antini, Afifah Rahma Dian, Risfidian Mohadi, and Aldes Lesbani. "An insight into the adsorption behavior of malachite green on DABCO (1,4-diazabicyclo[2.2.2]octane) modified bentonite." In 2ND INTERNATIONAL CONFERENCE ON CHEMISTRY, CHEMICAL PROCESS AND ENGINEERING (IC3PE). Author(s), 2018. http://dx.doi.org/10.1063/1.5064970.

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Šála, Michal, Milan Dejmek, Eliška Procházková, et al. "Novel conformationally locked nucleosides and oligonucleotides based on bicyclo[3.2.1]octane scaffold as a pseudosugar moiety." In XVIth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2014. http://dx.doi.org/10.1135/css201414379.

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