Relevant bibliographies by topics / Claisen rearrangement

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

Academic literature on the topic 'Claisen rearrangement'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 July 2025

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Journal articles on the topic "Claisen rearrangement"

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Zhang, Beibei, Xiaoxian Li, Boying Guo, and Yunfei Du. "Hypervalent iodine reagent-mediated reactions involving rearrangement processes." Chemical Communications 56, no. 91 (2020): 14119–36. http://dx.doi.org/10.1039/d0cc05354f.

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We summarize the developments of hypervalent iodine reagents-mediated reactions involving [1,2]-migration, Hofmann rearrangement, Beckmann rearrangement, ring contraction/expansion, [3,3]-sigmatropic/iodonium-Claisen rearrangement and some miscellaneous rearrangements.
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K., C. Majumdar, and Bhattacharyya Trijit. "Aza-Claisen rearrangement." Journal of Indian Chemical Society Vol. 79, Feb 2002 (2002): 112–21. https://doi.org/10.5281/zenodo.5840687.

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Department of Chemistry. University of Kalyani, Kalyani-741 235, India E-mail : kcm@klyuniv.ernet.in Fax : 91-033-5828282 <em>Manuscript received 28 February 2001. accepted 20 June 2001</em> This brief review presents an overview on aza-Claisen rearrangement with an emphasis on recent developments, e.g. ketene-aza-Claisen rearrangement, aza-Claisen rearrangement by acid-catalyzed Michael addition and palladium complex-catalyzed aza-Claisen rearrangement etc.
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McGeary, Ross, Jed Burns, and Elizabeth Krenske. "Claisen Rearrangements of Benzyl Vinyl Ethers and Heterobenzyl Vinyl Ethers." Synthesis 50, no. 09 (2018): 1750–72. http://dx.doi.org/10.1055/s-0036-1589529.

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The Claisen rearrangement of benzylic substrates (benzyl vinyl­ ethers) has received considerably less attention than its well-known aliphatic and normal aromatic variants. Here, we review the rearrangement of both benzylic and heterobenzylic substrates, with examples of the reaction’s use in the synthesis of natural products and drug-like molecules.1 Introduction2 Early Attempts at the Benzyl-Claisen Rearrangement3 Successful Benzylic Examples4 Heterobenzylic Examples5 Conclusion
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Ito, Hisanaka, and Takeo Taguchi. "Asymmetric Claisen rearrangement." Chemical Society Reviews 28, no. 1 (1999): 43–50. http://dx.doi.org/10.1039/a706415b.

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Takano, Seiichi, Shun’ichi Tomita, Michiyasu Takahashi, and Kunio Ogasawara. "Thionolactone Claisen Rearrangement." Chemistry Letters 16, no. 7 (1987): 1379–80. http://dx.doi.org/10.1246/cl.1987.1379.

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Saputra, Rizki Rachmad, Reny Rosalina, Dimas Pramudita, et al. "Claisen Rearrangement Toward Cyclic Compound on Different Organic Synthesis Methods: Short Review." Chempublish Journal 7, no. 2 (2023): 80–87. http://dx.doi.org/10.22437/chp.v7i2.26053.

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The synthesis of functional and complex organic compounds is majorly performed by the Claisen rearrangement method. Claisen rearrangement is one of [3,3] sigmatropic rearrangements, a complex method in the synthesis of organic compounds, where it is mostly used to construct stereoselective compounds. It can be combined with other synthesis methods to synthesize organic compounds giving satisfactory results based on the method used, temperature, time, and yield produced. This review aimed to summarize several recent advances in synthesizing organic compounds through Claisen rearrangement reacti
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Krištofíková, Dominika, Juraj Filo, Mária Mečiarová, and Radovan Šebesta. "Why do thioureas and squaramides slow down the Ireland–Claisen rearrangement?" Beilstein Journal of Organic Chemistry 15 (December 10, 2019): 2948–57. http://dx.doi.org/10.3762/bjoc.15.290.

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A range of chiral hydrogen-bond-donating organocatalysts was tested in the Ireland–Claisen rearrangement of silyl ketene acetals. None of these organocatalysts was able to impart any enantioselectivity on the rearrangements. Furthermore, these organocatalysts slowed down the Ireland–Claisen rearrangement in comparison to an uncatalyzed reaction. The catalyst-free reaction proceeded well in green solvents or without any solvent. DFT calculations showed that the activation barriers are higher for reactions involving hydrogen-donating organocatalysts and kinetic experiments suggest that the catal
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Jain, Seema. "Zinc Chloride Catalyzed Amino Claisen Rearrangement of 1-N-Allylindolines: An Expedient Protocol for the Synthesis of Functionalized 7-Allylindolines." Heterocyclic Communications 25, no. 1 (2019): 22–26. http://dx.doi.org/10.1515/hc-2019-0010.

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Abstract7-Allylindolines are valuable synthons for designing biologically active molecular libraries. Lewis acid catalyzed amino-Claisen rearrangement provides a one pot synthetic entry to these heteroarenes. In this context, Zinc chloride (ZnCl2)–N,N-dimethylformamide system efficiently catalyzed amino-Claisen rearrangements of 1-N-allylindolines to 7-allylindolines. The rearrangement is influenced by stereoelectronic effects of substituents present in 1-N-allylindolines. The substrates containing electron donating functionalities underwent rearrangement at lower temperature than substrates w
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Gopalan, B., K. Rajagopalan, K. Sunitha, and K. K. Balasubramanian. "Studies in claisen rearrangement." Tetrahedron 41, no. 15 (1985): 3153–59. http://dx.doi.org/10.1016/s0040-4020(01)96670-0.

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Ito, Hisanaka, Azusa Sato, and Takeo Taguchi. "Enantioselective aromatic Claisen rearrangement." Tetrahedron Letters 38, no. 27 (1997): 4815–18. http://dx.doi.org/10.1016/s0040-4039(97)01040-x.

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Dissertations / Theses on the topic "Claisen rearrangement"

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Yoon, Tehshik Peter MacMillan David W. C. "The acyl-Claisen rearrangement development of a novel metal-catalyzed Claisen rearrangement and enantioselective variants of the acyl-Claisen rearrangement /." Diss., Pasadena, Calif. : California Institute of Technology, 2002. http://resolver.caltech.edu/CaltechTHESIS:01282010-153053761.

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Thesis (Ph. D.)--California Institute of Technology, 2002. PQ #3052855.<br>Advisor names found in the Acknowledgments pages of the thesis. Title from home page. Viewed 02/11/2010. Includes bibliographical references.
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Mountford, David Mark. "Novel Claisen rearrangement reactions." Thesis, Imperial College London, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.415168.

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Yang, Yanbo. "Pd0-Catalyzed Formal 1,3-Diaza-Claisen Rearrangement. Design And Development Of Cationic 1,3-Diaza-Claisen Rearrangement." ScholarWorks @ UVM, 2014. http://scholarworks.uvm.edu/graddis/261.

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The dissertation describes Pd0-catalyzed formal 1,3-diaza-Claisen rearrangement and the design and development of cationic 1,3-diaza-Claisen rearrangement. Our previous work has shown that isocyanates react with azanorbornenes and azabicyclo[2.2.2]octenes under thermal conditions to afford zwitterionic intermediates that undergo a thermal 1,3-diaza-Claisen rearrangement to give both ureas and isoureas. However, some azanorbornenes and azabicyclooctenes failed to rearrange or proceeded in low yields. To address these challenging substrates for the thermal 1,3-diaza-Claisen rearrangement, we hav
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O'Brien, Alexander. "Acyclic stereocontrol in the Claisen rearrangement." Thesis, Imperial College London, 2010. http://hdl.handle.net/10044/1/5560.

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This thesis examines the issues of acyclic stereocontrol in the Claisen rearrangement, with particular emphasis on the effects of exopericyclic stereocentres – i.e. those adjacent to the array of atoms directly involved in the sigmatropic process. It is divided into three main parts: The first section provides a review of the field of acyclic stereocontrol. The models used to explain the development of relationships between stereocenters in systems lacking well-defined conformational constraints are discussed. This is an established field and particular emphasis is given to recent developments
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Mohamed, Mustafa Abdi. "Synthesis of [alpha]-allynyl and [alpha]-allylsilane amino acids by the Claisen rearrangement /." *McMaster only, 2001.

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Voûte, Nicholas. "Rearrangements in the indolo[2,3-b]quinoline system : a novel approach to the synthesis of perophoramidine and the communesins /." Thesis, St Andrews, 2008. http://hdl.handle.net/10023/486.

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Garcia-Torres, Jason. "Development of a dual Fries-Claisen rearrangement strategy." Thesis, Loughborough University, 2012. https://dspace.lboro.ac.uk/2134/11002.

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Synthetic approaches towards linear fused carbon rings have been developed over the last decades due to their high interest as compounds with potential antibiotic activity and as organic electronics. The application of a novel iterative route towards linear fused carbon ring systems could provide a versatile new mode of access to complex substituted ring systems. Studies have previously demonstrated the use of an allylation-double Claisen-RCM sequence to build fused carbon rings (C). In this thesis we described our work to expand the use of this methodology by developing milder reaction condit
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Neal, Andrew. "Use of the Claisen rearrangement in natural product synthesis." Thesis, University of St Andrews, 2018. http://hdl.handle.net/10023/16129.

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Fuhry, Mary Ann Monica. "The Claisen rearrangement route to octalactins A and B." Thesis, University of Cambridge, 1995. https://www.repository.cam.ac.uk/handle/1810/271938.

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Barmettler, Peter. "Säurekatalysierte Amino-Claisen-Umlagerungen von 2, 6-Disubstituierten N-Propargylanilinen." [Fribourg, Switzerland] : Institut für Organische Chemie, Universität Freiburg (Schweiz), 1985. http://catalog.hathitrust.org/api/volumes/oclc/21856572.html.

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Books on the topic "Claisen rearrangement"

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Martin, Hiersemann, and Nubbemeyer Udo, eds. The Claisen rearrangement: Methods and applications. Wiley-VCH, 2007.

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Garayt, Maxime. Manipulation of fluorinated building block[s] via [3,3]-claisen rearrangement. University of Birmingham, 2001.

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Davidson, Mark Murison. A theoretical investigation of the Claison rearrangement. University of Manchester, 1995.

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Moffat, Ella-Maria. Asymmetric induction allylstannanes: A study towards Ireland-Claisen rearrangements. University of Manchester, 1995.

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Dimartino, Gianluca. Ring expansion routes to cyclic fluoroketones by oxy-cope and claisen rearrangements. University of Birmingham, 2000.

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Hiersemann, Martin, and Udo Nubbemeyer, eds. The Claisen Rearrangement. Wiley, 2007. http://dx.doi.org/10.1002/9783527610549.

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Hiersemann, Martin, and Udo Nubbemeyer. Claisen Rearrangement: Methods and Applications. Wiley & Sons, Limited, John, 2007.

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Hiersemann, Martin, and Udo Nubbemeyer. Claisen Rearrangement: Methods and Applications. Wiley & Sons, Incorporated, John, 2007.

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(Editor), Martin Hiersemann, and Udo Nubbemeyer (Editor), eds. The Claisen Rearrangement: Methods and Applications. Wiley-VCH, 2007.

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Uyeda, Christopher Hiroki. Catalysis of the Claisen rearrangement by hydrogen-bond donors. 2010.

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Book chapters on the topic "Claisen rearrangement"

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Li, Jie Jack. "Claisen Rearrangement." In Name Reactions. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-50865-4_30.

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Li, Jie Jack. "Abnormal Claisen rearrangement." In Name Reactions. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_1.

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Li, Jie Jack. "Abnormal Claisen rearrangement." In Name Reactions. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_1.

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Craig, Donald. "The Claisen Rearrangement." In Molecular Rearrangements in Organic Synthesis. John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118939901.ch13.

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Rehbein, Julia, and Martin Hiersemann. "Catalytic Asymmetric Gosteli-Claisen Rearrangement (CAGC)." In Asymmetric Synthesis II. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527652235.ch21.

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Severance, Daniel L., and William L. Jorgensen. "Claisen Rearrangement of Allyl Vinyl Ether." In Structure and Reactivity in Aqueous Solution. American Chemical Society, 1994. http://dx.doi.org/10.1021/bk-1994-0568.ch017.

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Kobayashi, Takayoshi. "A New Reaction Mechanism of Claisen Rearrangement Induced by Few-Optical-Cycle Pulses." In Ultrashort Pulse Lasers and Ultrafast Phenomena. CRC Press, 2023. http://dx.doi.org/10.1201/9780429196577-80.

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Li, Jie Jack. "Claisen rearrangements." In Name Reactions. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_63.

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Li, Jie Jack. "Claisen rearrangements." In Name Reactions. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_56.

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"Claisen Rearrangement." In Laboratory Experiments Using Microwave Heating. CRC Press, 2013. http://dx.doi.org/10.1201/b14645-10.

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Conference papers on the topic "Claisen rearrangement"

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Grubbs II, G., Stewart Novick, S. Cooke, Daniel Obenchain, and Derek Frank. "CP-FTMW SPECTROSCOPY OF A CLAISEN REARRANGEMENT PRECURSOR ALLYL PHENYL ETHER." In 71st International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2016. http://dx.doi.org/10.15278/isms.2016.mi02.

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Rodrigues, Tiago C. A. F., Angelo H. L. Machado, and Wender Alves da Silva. "Methodological study of the classic Claisen rearrangement in Morita-Baylis-Hillman adducts." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_20139316573.

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Debnath, Pradip. "Regioselective Synthesis of Coumarin-Annulated Polycyclic Heterocycles via Sequential Claisen Rearrangement and Radical Cyclization Reaction." In ECSOC 2024. MDPI, 2024. https://doi.org/10.3390/ecsoc-28-20127.

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Golubenkova, Alexandra S., Nikita E. Golantsov, Alexey V. Varlamov, and Leonid G. Voskressensky. "Green synthesis of polysubstituted pyrroles through a domino sequence of aza-Claisen rearrangement/nucleophilic addition/oxidation/acylation." In ACTUAL PROBLEMS OF ORGANIC CHEMISTRY AND BIOTECHNOLOGY (OCBT2020): Proceedings of the International Scientific Conference. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0069005.

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Elečko, J., J. Gonda та M. Martinková. "Synthesis of 5-amino-α-D-gluco-hept-6-enfuranose as usefull 1-deoxynojirimycin precursor using [3,3]-sigmatropic aza-Claisen rearrangement". У The 14th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00418.

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Barham, Joshua Philip, Yasuo Norikane, Hiromichi Egami, and Yoshitaka Hamashima. "High Efficiency Microwave Flow Chemistry Towards Synthesis of Functional Materials and Pharmaceutical Cores." In Ampere 2019. Universitat Politècnica de València, 2019. http://dx.doi.org/10.4995/ampere2019.2019.9860.

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Microwave (MW) heating benefits organic synthesis by affording higher product yields in shorter time periods than conventional heating, yet it suffers from poor scalability and is limited to polar solvents in typical batch mode reactors. Herein, we report a microwave flow reactor using a solid-state semiconductor MW generator. The tunable, single-mode MW heating allows high efficiency, scalable organic synthesis, rapid reaction optimization and is applicable to non-polar solvents (o-Xylene and CPME can be rapidly heated to ca. 260 oC). Auto-frequency tuning compensates for changes in the micro
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Mues, H., and U. Kazmaier. "Via Ester Enolate Claisen Rearrangements To a Variety of Non-Proteinogenic Amino Acids." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01901.

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