Relevant bibliographies by topics / Staudinger [2+2] cycloaddition

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

Academic literature on the topic 'Staudinger [2+2] cycloaddition'

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

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Journal articles on the topic "Staudinger [2+2] cycloaddition"

1

He, Wei, Junpeng Zhuang, Zhanhui Yang, and Jiaxi Xu. "Sterically controlled diastereoselectivity in thio-Staudinger cycloadditions of alkyl/alkenyl/aryl-substituted thioketenes." Organic & Biomolecular Chemistry 15, no. 26 (2017): 5541–48. http://dx.doi.org/10.1039/c7ob01214d.

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Spruha, A. Gharad, and N. Berad Baliram. "Synthesis, characterization and antibacterial study of 1-arylamido-3-chloro-4- (2-chloroquinolin-3-yl)-azetidin-2-ones." Journal of Indian Chemical Society Vol. 93, Febr 2016 (2016): 223–28. https://doi.org/10.5281/zenodo.5603154.

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Post Graduate Teaching Department of Chemistry, Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur-440 033, Maharashtra, India <em>E-mail</em> : spruhagharad@gmail.com, bnberad@gmail.com <em>Manuscript received online 28 April 2015, revised 20 May 2015, accepted 22 May 2015</em> A series of quinoline based &beta;-lactams (azetidinones) have been synthesized via cycloaddition reaction (Staudinger reaction) of imines with ketene. The methodology involves [2+2] cycloaddition of Schiff bases with chloroacetyl chloride in presence of triethylamine to yield the corresponding 1-arylamido-3-chloro
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Bakulina, Olga, Dmitry Dar'in та Mikhail Krasavin. "Mixed carboxylic–sulfonic anhydride in reaction with imines: a straightforward route to water-soluble β-lactams via a Staudinger-type reaction". Organic & Biomolecular Chemistry 16, № 21 (2018): 3989–98. http://dx.doi.org/10.1039/c8ob00768c.

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The first example of employing a mixed carboxylic–sulfonic anhydride in reaction with imines is reported. It gave β-lactams, presumably, via a formal [2 + 2] cycloaddition (a Staudinger-type reaction).
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Lu, Nan, Chengxia Miao та Xiaozheng Lan. "Theoretical investigation on diastereoselective [2+2] cycloaddition and Pd-catalyzed enantioselective [3+2] cycloaddition for synthesis of cis-β-lactam and exo-furobenzopyranone". Thermal Science and Engineering 7, № 1 (2024): 5949. http://dx.doi.org/10.24294/tse.v7i1.5949.

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The mechanism is investigated for Wolff rearrangement/Staudinger [2+2] cycloaddition cascade and Pd-catalyzed, decarboxylative, formal [3+2] cycloaddition. Wolff rearrangement of 3-diazotetramic acid is determined to be rate-limiting step generates cyclic acyl ketene. The interaction of ketene with imine firstly results in zwitterion followed by conrotatory cyclization giving major cis-β-lactam. For synthesis of s-VECs, the epoxidation−cyclization cascade and hydrolysis give precursor of better performing exocyclic derivative. The reaction with 3-cyanochromone includes decarboxylation, nucleop
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Ram, Naresh Yadav, Banik Indrani та Krishna Banik Bimal. "Microwave-induced new synthesis of trans and cis 3-phenylthio-4-carboethoxy β-lactams". Journal of Indian Chemical Society Vol. 96, Oct 2019 (2019): 1355–58. https://doi.org/10.5281/zenodo.5642731.

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Department of Chemistry, Faculty of Engineering and Technology, Veer Bahadur Singh Purvanchal University, Jaunpur-222 003, Uttar Pradesh, India Department of Chemistry, University of Texas-Pan American,1201 W. University Dr., Edinburg, TX 78539, USA The University of Texas-M. D. Anderson Cancer Center, Department of Molecular Pathology, 1515 Holcombe Blvd, Houston, TX 77030, USA Department of Mathematics and Natural Sciences, College of Sciences and Human Studies, Prince Mohammad Bin Fahd University, Al Khobar, Kingdom of Saudi Arabia <em>E-mail</em>: bimalbanik10@gmail.com, bbanik@pmu.edu.sa
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Jarrahpour, Aliasghar, Mohammad Mahdi Doroodmand, and Edris Ebrahimi. "The first report of [2+2] ketene–imine cycloaddition reactions (Staudinger) on carbon nanotubes." Tetrahedron Letters 53, no. 23 (2012): 2797–801. http://dx.doi.org/10.1016/j.tetlet.2012.03.089.

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Ram, Naresh Yadav, Kumar Singh Amarendra, Banik Indrani та Krishna Banik Bimal. "Microwave-induced stereospecific synthesis of trans 3-phenylthio β-lactams". Journal of Indian Chemical Society Vol. 96, Oct 2019 (2019): 1359–63. https://doi.org/10.5281/zenodo.5642753.

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Department of Chemistry, Faculty of Engineering and Technology, Veer Bahadur Singh Purvanchal University, Jaunpur-222 003, Uttar Pradesh India Department of Chemistry, University of Texas-Pan American, 1201 W. University Dr., Edinburg, TX 78539, USA The University of Texas-M. D. Anderson Cancer Center, Department of Molecular Pathology, 1515 Holcombe Blvd, Houston, TX 77030, USA Department of Mathematics and Natural Sciences, College of Sciences and Human Studies, Prince Mohammad Bin Fahd University, Al Khobar, Kingdom of Saudi Arabia <em>E-mail:</em> bimalbanik10@gmail.com; bbanik@pmu.edu.sa
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Leier, Samantha, and Frank Wuest. "Innovative Peptide Bioconjugation Chemistry with Radionuclides: Beyond Classical Click Chemistry." Pharmaceuticals 17, no. 10 (2024): 1270. http://dx.doi.org/10.3390/ph17101270.

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Background: The incorporation of radionuclides into peptides and larger biomolecules requires efficient and sometimes biorthogonal reaction conditions, to which click chemistry provides a convenient approach. Methods: Traditionally, click-based radiolabeling techniques have focused on classical click chemistry, such as copper(I)-catalyzed alkyne-azide [3+2] cycloaddition (CuAAC), strain-promoted azide-alkyne [3+2] cycloaddition (SPAAC), traceless Staudinger ligation, and inverse electron demand Diels–Alder (IEDDA). Results: However, newly emerging click-based radiolabeling techniques, includin
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Fernández, Rosario, Ana Ferrete, José M. Lassaletta, José M. Llera, and Eloísa Martín-Zamora. "N,N-Dialkylhydrazones as the Imine Component in the Staudinger-Like [2+2] Cycloaddition to Benzyloxyketene." Angewandte Chemie 114, no. 5 (2002): 859–61. http://dx.doi.org/10.1002/1521-3757(20020301)114:5<859::aid-ange859>3.0.co;2-k.

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Barba, Victor, Cecilia Hernández, Susana Rojas-Lima, Norberto Farfán та Rosa Santillan. "Preparation of N-aryl-substituted spiro-β-lactams via Staudinger cycloaddition". Canadian Journal of Chemistry 77, № 12 (1999): 2025–32. http://dx.doi.org/10.1139/v99-212.

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The interest in the study of β-lactams continues due to their therapeutic importance as antibiotics. In this work, six spiro-β-lactams (7a-7c, 8a-8c) have been prepared using the [2+2] cycloaddition of isomaleimides to acid chlorides. The heterobicyclic structures obtained have been characterized by mass spectrometry, IR, NMR spectroscopy, and for compounds 7a, 7b, and 8b the X-ray crystallographic study showed a nearly planar arrangement for the β-lactam ring.Key words: β-lactams, azetidinone, isomaleimides, ketenes, X-ray crystallography.
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Dissertations / Theses on the topic "Staudinger [2+2] cycloaddition"

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Wan, Honghe. "Allenes and (2+2+1) cycloaddition reactions." Morgantown, W. Va. : [West Virginia University Libraries], 1998. http://etd.wvu.edu/templates/showETD.cfm?recnum=195.

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Thesis (M.S.)--West Virginia University, 1998.<br>Title from document title page. Document formatted into pages; contains xii, 99 p. : ill. Includes abstract. Includes bibliographical references (p. 93-99).
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Haraburda, Ewelina. "[2+2+2] cycloaddition reactions involving allenes catalysed by rhodium." Doctoral thesis, Universitat de Girona, 2015. http://hdl.handle.net/10803/328439.

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The development of new chemical processes for the formation of carbon-carbon bonds is an important topic in organic chemistry. In particular, the transition metal catalysed [2+2+2] cycloaddition reaction is a highly efficient synthetic tool that allows six-membered polysubstituted carbo- and heterocyclic derivatives to be obtained in an atom economy process. Allenes are versatile substrates for cycloaddition reactions that provide a good reactivity profile together with the ability to increase the stereochemical complexity of the cycloadducts obtained. This doctoral thesis, divided into seven
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Parera, Briansó Magda. "Transition metal-catalysed [2+2+2] cycloaddition reactions. Methodology and mechanism." Doctoral thesis, Universitat de Girona, 2014. http://hdl.handle.net/10803/145035.

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The transition-metal catalysed [2+2+2] cycloaddition reaction is a highly efficient synthetic tool that allows six-membered polysubstituted carbo- and heterocyclic derivatives to be obtained in an atom economy process. This doctoral thesis is based on methodological and mechanistic studies of the rhodium(I)-catalysed [2+2+2] cycloaddition reaction. In particular, the use of hemilabile S-stereogenic and P-stereogenic ligands for the rhodium-catalysed [2+2+2] cycloaddition is described. The activity of these new catalytic systems is evaluated in the cycloaddition of three alkynes and in the enan
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Fernández, Wang Martí. "New challenges in Rh(I)-catalysed [2+2+2] cycloaddition reactions." Doctoral thesis, Universitat de Girona, 2017. http://hdl.handle.net/10803/663661.

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This doctoral thesis studies the involvement of challenging unsaturated substrates in the transition-metal catalysed [2+2+2] cycloaddition reaction, as well as new catalytic systems for the reaction. First, Morita-Baylis-Hillman adducts are involved in the partial intramolecular rhodium(I)-catalysed [2+2+2] cycloaddition reaction. Next, linear chiral allene-yne/ene-allene substrates are synthesized and submitted to [2+2+2] cycloaddition reaction conditions. The process works with effective chirality induction of the chiral centres of the linear compounds to the cycloadducts. Following, the syn
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姚大源 and Tai-yuen Yue. "Cycloaddition reactions of 2-vinylchromones." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1992. http://hub.hku.hk/bib/B31210661.

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Allart, Eric A. "Metal-promoted [3+2] and [4+2] cycloaddition reactions." Thesis, Loughborough University, 2008. https://dspace.lboro.ac.uk/2134/33615.

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Dicobalt complexes have been extensively used in synthetic chemistry to protect triple bonds, to form new carbon/carbon bonds using the Nicholas reaction and to form polycyclic molecules using the Pauson-Khand reaction. Using these dicobalt complexes, the formation of new carbon-heteroatom bonds was developed through [3+2] and [4+2] cycloaddition reactions via a stabilised dipole intermediate. Initial work carried out makes use of cyclopropanes substituted with a metal-alkyne complex towards the synthesis of tetrahydrofurans and pyrrolidines in good yields and with acceptable diastereoselectiv
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Dachs, Soler Anna. "Rhodium(I) catalyzed [2+2+2] cycloaddition reactions: experimental and theoretical studies." Doctoral thesis, Universitat de Girona, 2011. http://hdl.handle.net/10803/52981.

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The [2+2+2] cycloaddition reaction involves the formation of three carbon-carbon bonds in one single step using alkynes, alkenes, nitriles, carbonyls and other unsaturated reagents as reactants. This is one of the most elegant methods for the construction of polycyclic aromatic compounds and heteroaromatic, which have important academic and industrial uses. The thesis is divided into ten chapters including six related publications. The first study based on the Wilkinson’s catalyst, RhCl(PPh3)3, compares the reaction mechanism of the [2+2+2] cycloaddition process of acetylene with the cycloaddi
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Garcia, Pierre. "Formation d'aminopyridines par cycloaddition [2+2+2] catalysée par des complexes du cobalt." Paris 6, 2013. http://www.theses.fr/2010PA066750.

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LLERENA, DOMINIQUE. "Reactions de cycloaddition (2+2+2) d'allenediynes catalysees par des complexes du cobalt (i)." Paris 6, 1995. http://www.theses.fr/1995PA066378.

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Des allenediynes diversement substitues, dont les syntheses originales sont decrites ont ete engages avec des quantites stoechiometriques de cpco(co)#2 dans des reactions de cycloaddition (2+2+2). Ces reactions ont permis la synthese de structures tricycliques analogues des cycles abc ou bcd de steroides. Par ailleurs, cette etude a permis de mettre en evidence une nouvelle catalyse de la ene-reaction par le cobalt mettant en jeu des composes allenynes
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Karupaiyan, K. "Diastereoselective staudinger reaction for the synthesis of azetidine-2-ones." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 2001. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/2407.

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Books on the topic "Staudinger [2+2] cycloaddition"

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Davidson, Tony. Studies in the cobalt catalyzed [2+2+2+2] cycloaddition and deprotonation of dicobalt hexacarbonyl-acetylene complexes. National Library of Canada, 1990.

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2

Joseph Johannes Gerardus Steven van Es. 1, 3-cycloaddition reactions of diphenylphosphinoyl-activated azomethine ylides and 2-azaallyl anions: Synthetic applications and mechanistic aspects. Pasmans Offsetdrukkerij BV, 1992.

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Advances in Cycloaddition, Volume 2 (Advances in Cycloaddition). JAI Press, 1990.

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Cä, Simon mmerer, and Simon Cämmerer. Die Eisen-Vermittelte [2+2+1]-Cycloaddition Zum Aufbau Von Indolochinolizidinalkaloiden. Tectum Verlag, 2012.

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Oetker, Hartmut, Dirk Neumann, Julius von Staudinger, and Ulrich Preis. Staudinger, Julius von, Buch 2, Recht der Schuldverhältni : Paragraphen 616-630. Gruyter, 2002.

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6

Kleen, Astrid. Pericyclische Reaktionen an Kohlenhydraten: [2+2]-Cycloaddition mit Dichlorketen an Kohlenhydrat-Enolether ; Synthese von C-Glycosiden über chirale Cyclobutanone. 1992.

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7

Andriotis, A. N., R. M. Sheetz, E. Richter, and M. Menon. Structural, electronic, magnetic, and transport properties of carbon-fullerene-based polymers. Edited by A. V. Narlikar and Y. Y. Fu. Oxford University Press, 2017. http://dx.doi.org/10.1093/oxfordhb/9780199533053.013.21.

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This article discusses the structural, electronic, magnetic, and transport properties of carbon-fullerene-based polymers. In particular, it examines the defect-induced ferromagnetism of the C60-based polymers and its analog in the case of non-traditional inorganic materials. It first reviews the computational methods currently used in the literature, highlighting the pros and cons of each one of them. It then considers the defects associated with the ferromagnetism of the C60-based polymers, namely carbon vacancies, the 2 + 2 cycloaddition bonds and impurity atoms, and their effect on the elec
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Zellenberg, Ulrich. Österreichisches Bundesverfassungsrecht. Edited by Kark Korinek, Michael Holoubek, Christoph Bezemek, Claudia Fuchs, and Andrea Martin. Verlag Österreich, 2021. http://dx.doi.org/10.33196/9783704687425.

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Der von Karl Korinek und Michael Holoubek begründete Großkommentar bietet traditionell eine ebenso umfassende wie profunde Aufarbeitung des österreichischen Verfassungsrechts. Was vor mehr als zwanzig Jahren als Pionierprojekt begonnen hat, ist mittlerweile zum bestimmenden Referenzwerk für Wissenschaft und Praxis geworden. Der zwischenzeitlich um Christoph Bezemek, Claudia Fuchs, Andrea Martin und Ulrich E. Zellenberg ergänzte Kreis der Herausgeberinnen und Herausgeber verfolgt nach wie vor konsequent jenen Anspruch, der das Werk seit jeher ausgezeichnet hat: die Verbindung von unbedingter wi
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Book chapters on the topic "Staudinger [2+2] cycloaddition"

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Laue, Thomas, and Andreas Plagens. "[2+2] Cycloaddition." In Teubner Studienbücher Chemie. Vieweg+Teubner Verlag, 1994. http://dx.doi.org/10.1007/978-3-322-94015-5_28.

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Laue, Thomas, and Andreas Plagens. "[2+2]Cycloaddition." In Teubner Studienbücher Chemie. Vieweg+Teubner Verlag, 1998. http://dx.doi.org/10.1007/978-3-322-94077-3_29.

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Laue, Thomas, and Andreas Plagens. "[2+2]Cycloaddition." In Teubner Studienbücher Chemie. Vieweg+Teubner Verlag, 1994. http://dx.doi.org/10.1007/978-3-322-94726-0_28.

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Hayashi, Yujiro, and Koichi Narasaka. "[2+2] Cycloaddition Reactions." In Comprehensive Asymmetric Catalysis I–III. Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-642-58571-5_10.

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Gandon, Vincent. "Cobalt-Mediated [2 + 2 + 2] Cycloaddition." In Transition-Metal-Mediated Aromatic Ring Construction. John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118629871.ch1.

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Kumar, Puneet, and Janis Louie. "Nickel-Mediated [2 + 2 + 2] Cycloaddition." In Transition-Metal-Mediated Aromatic Ring Construction. John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118629871.ch2.

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Yamamoto, Yoshihiko. "Ruthenium-Mediated [2 + 2 + 2] Cycloaddition." In Transition-Metal-Mediated Aromatic Ring Construction. John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118629871.ch3.

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Tanaka, Ken. "Rhodium-Mediated [2 + 2 + 2] Cycloaddition." In Transition-Metal-Mediated Aromatic Ring Construction. John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118629871.ch4.

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Takeuchi, Ryo. "Iridium-Mediated [2 + 2 + 2] Cycloaddition." In Transition-Metal-Mediated Aromatic Ring Construction. John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118629871.ch5.

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Brogaard, Rasmus Y. "Paracyclophanes I: [2 $$+$$ 2]cycloaddition of Ethylenes." In Molecular Conformation and Organic Photochemistry. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-29381-8_7.

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Conference papers on the topic "Staudinger [2+2] cycloaddition"

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Gómez- Campillos, Gonzalo, Cristina Aragoncillo, Pedro Almendros, and Benito Alcaide. "Pd−Catalyzed Domino Alkyne Dimerization/Double [2+2] Allenyne Cycloaddition." In The 13th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2009. http://dx.doi.org/10.3390/ecsoc-13-00252.

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Mancini, Pedro, Claudia Della Rosa, and Maria Kneeteman. "Behaviour of 2-nitroheterocycles in Cycloaddition Reactions." In The 9th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2005. http://dx.doi.org/10.3390/ecsoc-9-01477.

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Förster, Nadja, Ann-Christin Pöppler, and Philipp Vana. "UV-induced [2+2]-cycloaddition for shell-formation of star polymers." In 6TH INTERNATIONAL CONFERENCE ON TIMES OF POLYMERS (TOP) AND COMPOSITES. AIP, 2012. http://dx.doi.org/10.1063/1.4738496.

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Montero-Campillo, M., Jesús Rodríguez-Otero, and Enrique Cabaleiro-Lago. "Selectivity of the Ru(II)-Catalyzed [2+2+2] Cycloaddition of 1,6-Diynes and Tricarbonyl Compounds." In The 12th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01286.

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Rajzmann, Michel, Agnés Pommier, Jean-Marc Pons, Philippe Thomas, and André Baldy. "A semiempirical theoretical study of the [2+2] cycloaddition between ketene and formaldehyde." In The first European conference on computational chemistry (E.C.C.C.1). AIP, 1995. http://dx.doi.org/10.1063/1.47652.

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Yi, Jun, Junpeng Wang, and Zhou Lin. "MECHANISTIC STUDY OF PHOTOCHEMICAL [2+2] CYCLOADDITION BETWEEN 1,5-CYCLOOCTADIENE AND MALEIC ANHYDRIDE." In 2022 International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2022. http://dx.doi.org/10.15278/isms.2022.rh11.

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Montero­Campillo, M., Enrique Cabaleiro­Lago, and Jesús Rodríguez­Otero. "On the Mechanism of Rhodium-Catalyzed [6+2] Cycloaddition of 2-Vinylcylobutanones and Alknenes." In The 11th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2007. http://dx.doi.org/10.3390/ecsoc-11-01369.

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Barcellos, Júlio C. F., Ayres G.Dias, and Paulo R. R.Costa. "Synthesis of Azapterocarpan Analogues by Intramolecular 1,3-dipolar Cycloaddition." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0090-2.

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Sheradsky, Tuvia, and Elliad Silcoff. "The Synthesis of (2R,5R)-2-Amino-5-Hydroxyhexanoic Acid by Intermolecular Cycloaddition." In The 1st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 1997. http://dx.doi.org/10.3390/ecsoc-1-02026.

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Ramasami, Ponnadurai, Hanusha Bhakhoa, and Lydia Rhyman. "Copper(I) Catalyzed [3+2] Cycloaddition Reaction with Mechanistic Disparity: A DFT Study." In The 17th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-e017.

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