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Relevant bibliographies by topics / Halocyclization

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Journal articles
Dissertations / Theses
Book chapters

Academic literature on the topic 'Halocyclization'

Author: Grafiati

Published: 4 June 2021

Last updated: 11 March 2023

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Journal articles on the topic "Halocyclization"

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Moschona, Fotini, Christina Misirlaki, Nikolaos Karadimas, Maria Koutiva, Ioanna Savvopoulou, and Gerasimos Rassias. "Organocatalytic Asymmetric Halocyclization of Allylic Amides to Chiral Oxazolines Using DTBM-SEGPHOS—Mechanistic Implications from Hammett Plots." Symmetry 14, no. 5 (2022): 989. http://dx.doi.org/10.3390/sym14050989.

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The intramolecular halocyclization of alkenes possessing an internal heteroatom nucleophile leads to multifunctional heterocycles which are useful versatile intermediates in organic synthesis. The asymmetric chlorocyclisation of 2-substituted allylic amides gives access to chiral oxazolines bearing a chloromethyl moiety for further synthetic manipulation. The literature reports on this transformation involve complex syntheses of the 2-substituted allylic amides and cryogenic temperatures for achieving high enantioselectivities in the organocatalyzed halocyclization step. Based on the Heck reac

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2

de Andrade, Vitor, and Marcio de Mattos. "N-Halo Reagents: Modern Synthetic Approaches for Heterocyclic Synthesis." Synthesis 51, no. 09 (2019): 1841–70. http://dx.doi.org/10.1055/s-0037-1611746.

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Heterocyclic chemistry is an essential frontier in science and a source of novel biologically active compounds. The development of innovative synthetic methodologies that allows access to different heterocyclic rings is of critical interest to the scientific community. This review will focus on recent applications of N-halo compounds (e.g., N-halosuccinimides, trihaloisocyanuric acids, N-halosulfonamides, etc.) in heterocyclic construction via electrophilic cyclization, asymmetric halocyclization, oxidative cyclization, and radical processes.1 Introduction2 N-Halo Reagent Mediated Heterocyclic

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3

Kim, D. G. "Halocyclization of 2-allylthiobenzothiazole." Chemistry of Heterocyclic Compounds 34, no. 4 (1998): 505. http://dx.doi.org/10.1007/bf02290898.

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Kim, D. G. "Halocyclization of 2-allylthiopyridine." Chemistry of Heterocyclic Compounds 35, no. 3 (1999): 290–92. http://dx.doi.org/10.1007/bf02259357.

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Kim, D. G. "Halocyclization of 8-allylthioquinoline." Chemistry of Heterocyclic Compounds 33, no. 8 (1997): 989–91. http://dx.doi.org/10.1007/bf02253176.

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Subba Reddy, B. V., R. Anji Babu, B. Jagan Mohan Reddy, et al. "A short and highly convergent approach for the synthesis of rutaecarpine derivatives." RSC Advances 5, no. 35 (2015): 27476–80. http://dx.doi.org/10.1039/c4ra14093a.

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Xu, Jun, and Rongbiao Tong. "An environmentally friendly protocol for oxidative halocyclization of tryptamine and tryptophol derivatives." Green Chemistry 19, no. 13 (2017): 2952–56. http://dx.doi.org/10.1039/c7gc01341h.

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Zhang, Zhi-Qiang, and Feng Liu. "CuX2-mediated oxybromination/aminochlorination of unsaturated amides: synthesis of iminolactones and lactams." Organic & Biomolecular Chemistry 13, no. 24 (2015): 6690–93. http://dx.doi.org/10.1039/c5ob00520e.

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Yan, Jiahang, Zhiqiang Zhou, Qiaoqiao He, Guzhou Chen, Hongbo Wei, and Weiqing Xie. "The applications of catalytic asymmetric halocyclization in natural product synthesis." Organic Chemistry Frontiers 9, no. 2 (2022): 499–516. http://dx.doi.org/10.1039/d1qo01395e.

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Catalytic asymmetric halocyclization of olefinic substrate has evolved rapidly and been well utilized as a practical strategy for constructing enantioenriched cyclic skeletons in natural product synthesis.

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Fujioka, Hiromichi, and Kenichi Murai. "Recent Progress in Organocatalytic Asymmetric Halocyclization." HETEROCYCLES 87, no. 4 (2013): 763. http://dx.doi.org/10.3987/rev-12-762.

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Dissertations / Theses on the topic "Halocyclization"

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Reineke, Jana [Verfasser]. "Enantioselective Allylation and Halocyclization of Allyl Hydrazides and Allyl Oximes for the Synthesis of Enantioenriched Pyrazolidines and Isoxazolidines / Jana Reineke." Düsseldorf : Universitäts- und Landesbibliothek der Heinrich-Heine-Universität Düsseldorf, 2019. http://d-nb.info/1188017675/34.

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Pattarozzi, Mariella. "Highly chemo and stereoselective functionalizations of (S)-allyl-alanine." Doctoral thesis, Università degli studi di Padova, 2008. http://hdl.handle.net/11577/3425558.

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Steinmann, Jens G. "Halocyclization reactions a new approach to the synthesis of cyclic sulfates /." 1999. http://catalog.hathitrust.org/api/volumes/oclc/43743032.html.

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Strom, Kyle. "Halocyclizations and cycloisomerizations of 1,6-diynes, and sequence-defined, self-replicating polymers." Thesis, 2017. https://hdl.handle.net/2144/20866.

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The exploration of chemical space in search of molecules that perturb or mimic biological systems is essential to understanding human biology. The first part of this dissertation (Chapters 1-4) describes efforts to aid in the exploration of biologically relevant space through the invention of new π-cyclization methodologies. This strategy can be viewed as part of a “top-down” approach to investigating biology: the construction of small molecule drugs or probes which modify the behavior of the existing system. The second part of this dissertation (Chapter 5) describes preliminary efforts to exp

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Book chapters on the topic "Halocyclization"

1

Nubbemeyer, U. "Addition to Alkynes/Halocyclization." In X-Ene-X (X=F, Cl, Br, I, O, S, Se, Te, N, P), Ene-Hal, and Ene-O Compounds. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-032-00141.

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Jung, K. W., and A. S. Nagle. "Halocyclization of -Allyl Dithiocarbonate -Esters." In Four Carbon-Heteroatom Bonds. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-018-00524.

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"5.4 Halogenation and Halocyclization of Alkenes." In Catalytic Oxidation in Organic Synthesis, edited by Muñiz. Georg Thieme Verlag, 2018. http://dx.doi.org/10.1055/sos-sd-225-00195.

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Block, E. "From Halocyclizations." In Ene-X Compounds (X=S, Se, Te, N, P). Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-033-00216.

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