Academic literature on the topic 'Carbocyclic compounds'

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Journal articles on the topic "Carbocyclic compounds"

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Murarka, Sandip, and Andrey Antonchick. "Metal-Catalyzed Oxidative Coupling of Ketones and Ketone Enolates." Synthesis 50, no. 11 (2018): 2150–62. http://dx.doi.org/10.1055/s-0037-1609715.

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Recent years have witnessed a significant advancement in the field of radical oxidative coupling of ketones towards the synthesis of highly useful synthetic building blocks, such as 1,4-dicarbonyl compounds, and biologically important heterocyclic and carbocyclic compounds. Besides oxidative homo- and cross-coupling of enolates, other powerful methods involving direct C(sp3)–H functionalizations of ketones­ have emerged towards the synthesis of 1,4-dicarbonyl compounds. Moreover, direct α-C–H functionalization of ketones has also allowed an efficient access to carbocycles and heterocycles. Thi
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Sidi Mohamed, Bemba, Christian Périgaud, and Christophe Mathé. "Revaluation of biomass-derived furfuryl alcohol derivatives for the synthesis of carbocyclic nucleoside phosphonate analogues." Beilstein Journal of Organic Chemistry 13 (February 9, 2017): 251–56. http://dx.doi.org/10.3762/bjoc.13.28.

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The racemic synthesis of new carbocyclic nucleoside methylphosphonate analogues bearing purine bases (adenine and guanine) was accomplished using bio-sourced furfuryl alcohol derivatives. All compounds were prepared using a Mitsunobu coupling between the heterocyclic base and an appropriate carbocyclic precursor. After deprotection, the compounds were evaluated for their activity against a large number of viruses. However, none of them showed significant antiviral activity or cytotoxicity.
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Biteau, Nicolas G., Sarah A. Amichai, Niloufar Azadi, et al. "Synthesis of 4′-Substituted Carbocyclic Uracil Derivatives and Their Monophosphate Prodrugs as Potential Antiviral Agents." Viruses 15, no. 2 (2023): 544. http://dx.doi.org/10.3390/v15020544.

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Over the past decades, both 4′-modified nucleoside and carbocyclic nucleoside analogs have been under the spotlight as several compounds from either family showed anti-HIV, HCV, RSV or SARS-CoV-2 activity. Herein, we designed compounds combining these two features and report the synthesis of a series of novel 4′-substituted carbocyclic uracil derivatives along with their corresponding monophosphate prodrugs. These compounds were successfully prepared in 19 to 22 steps from the commercially available (-)-Vince lactam and were evaluated against a panel of RNA viruses including SARS-CoV-2, influe
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Ando, Wataru. "Polyorganosilicon Compounds in Strained Carbocyclic Systems." Bulletin of the Chemical Society of Japan 69, no. 1 (1996): 1–16. http://dx.doi.org/10.1246/bcsj.69.1.

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Yavari, Issa, and Aliyeh Khajeh-Khezri. "Recent Advances in the Synthesis of Hetero- and Carbocyclic Compounds­ and Complexes Based on Acenaphthylene-1,2-dione." Synthesis 50, no. 20 (2018): 3947–73. http://dx.doi.org/10.1055/s-0037-1610209.

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Acenaphthylene-1,2-dione has been utilized in a wide range of reactions as a starting material for the synthesis of hetero- and carbocyclic compounds and complexes. This review provides a short summary of the recent advances in the application of acenaphthylene-1,2-dione in the synthesis of hetero- and carbocyclic systems and bioactive compounds. In addition, the applications of acenaphthylene-1,2-dione in the synthesis of spiro compounds, propellanes, and ligands in catalyst reactions, from 2002 to early 2018, are included.1 Introduction2 Synthesis of Spiro Compounds Employing Acenaphthylene-
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Gaber, Hatem M., Mark C. Bagley, Zeinab A. Muhammad, and Sobhi M. Gomha. "Recent developments in chemical reactivity of N,N-dimethylenamino ketones as synthons for various heterocycles." RSC Advances 7, no. 24 (2017): 14562–610. http://dx.doi.org/10.1039/c7ra00683g.

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Halimehjani, Azim Ziyaei, Irishi N. N. Namboothiri, and Seyyed Emad Hooshmand. "Nitroalkenes in the synthesis of carbocyclic compounds." RSC Advances 4, no. 59 (2014): 31261. http://dx.doi.org/10.1039/c4ra04069d.

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Bartulewic, D., A. Markowska, S. Wołczyński, M. Dabrowska, and A. Rózański. "Molecular modelling, synthesis and antitumour activity of carbocyclic analogues of netropsin and distamycin--new carriers of alkylating elements." Acta Biochimica Polonica 47, no. 1 (2000): 23–35. http://dx.doi.org/10.18388/abp.2000_4059.

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A series of netropsin and distamycin analogues was synthesised and investigated by molecular modelling. The lowest-energy conformations of four carbocyclic lexitropsins, potential carriers of alkylating elements, were obtained using the HyperChem 4.0 program, and compared with the DNA-lexitropsin crystal structures from the Brookhaven National Laboratory Protein Data Bank. A method for synthesis of carbocyclic lexitropsins was elaborated, with the use of a nitro group or azobenzene as precursors for the aromatic amino group. The influence of methoxy group in ortho position with respect to amid
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Niu, Ben, Yin Wei та Min Shi. "Recent advances in annulation reactions based on zwitterionic π-allyl palladium and propargyl palladium complexes". Organic Chemistry Frontiers 8, № 13 (2021): 3475–501. http://dx.doi.org/10.1039/d1qo00273b.

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Carbocyclic and heterocyclic compounds could be constructed through the palladium-catalyzed annulation reactions of zwitterionic π-allyl palladium or propargyl palladium complexes with unsaturated electrophiles.
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Liu, Yuxiao, Yu Liu, Charles S. Shanahan, Xichen Xu, and Michael P. Doyle. "A survey of enoldiazo nucleophilicity in selective C–C bond forming reactions for the synthesis of natural product-like frameworks." Org. Biomol. Chem. 12, no. 28 (2014): 5227–34. http://dx.doi.org/10.1039/c4ob00709c.

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Dissertations / Theses on the topic "Carbocyclic compounds"

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Phun, Lien Hoang. "Innovative approaches to carbocyclic and heterocyclic compounds using strained carbocycles." Diss., Georgia Institute of Technology, 2013. http://hdl.handle.net/1853/47542.

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Natural products and small molecules play a major role in drug development. However, using natural products as a source of medicine comes with many challenges, such as lack of natural abundance and difficulty in isolation. Consequently, synthetic organic chemistry is a solution in order to access these compounds in usable quantities. However, synthetic chemisty comes with its own challenges such as efficiency, chemoselectivity, stereoselectivity and enantioselectivity. Therefore, synthetic tools that addresses these challenges are required solve these limitations. This thesis discusses new met
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Das, Jayanta. "Trans formative reactions on carbocyclic compounds." Thesis, University of North Bengal, 2015. http://ir.nbu.ac.in/handle/123456789/1863.

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Ghosh, Pranab. "Studies on chemical reactions of carbocyclic compounds." Thesis, University of North Bengal, 1991. http://hdl.handle.net/123456789/767.

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Bright, Steven. "Acid induced cationic rearrangements of carbocyclic compounds." Thesis, University of Canterbury. Chemistry, 1988. http://hdl.handle.net/10092/7597.

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This thesis examines fluorosulfonic acid as a reagent for use in organic synthesis. The acid strength of fluorosulfonic acid gives access to rearrangement products not available with weaker acids. The reaction of a selected series of benzyl carbinols with HSO₃F are reported. Reaction of 1-benzyl-2-methylcyclohexanol (1) gave cis-4a-methyl-1,2,3,4,4a,9a-hexahydrofluorene (2), while 1-benzyl -3-methylcyclohexanol (10) and 1-benzyl-4-methylcyclohexanol (11) were reduced to cis-1-benzyl-3-methylcyclohexane (12) and trans-1-benzyl-4-methylcyclohexane (13) respectively. [Diagram in thesis] 6-Ben
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Van, Eeden Nestor. "Synthesis of some potential antimicrobial carbocyclic compounds." Thesis, Cape Technikon, 1994. http://hdl.handle.net/20.500.11838/745.

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Thesis (M. Diploma in Technology (Chemistry))--Cape Technikon, 1994<br>Some naturally occurring compounds containing the naphtho [2,3 - c] pyran ring system have been found to be useful antibiotic agents and thus the laboratory synthesis ofthese compounds and their derivatives are of importance in the medical field. Their antibiotic and even antineoplastic activities are attributed to their potential to act as alkylating agents, via a bioreductive process. This thesis deals with studies directed towards the synthesis of some benzo [c] pyrans as these compounds also possess the correct st
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Pradhan, Nagendra Narayan. "Studies on the chemical reactions of carbocyclic compounds." Thesis, University of North Bengal, 2002. http://hdl.handle.net/123456789/743.

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Mothay, jyotsna. "Studies on the transformative reactions of carbocyclic compounds." Thesis, University of North Bengal, 2002. http://hdl.handle.net/123456789/771.

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Singha, Rabindranath. "Chemical transformation of carbocyclic compounds and development of novel reaction protocols." Thesis, University of North Bengal, 2021. http://ir.nbu.ac.in/handle/123456789/4326.

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Dutta, Gopal. "Chemical investigation of naturally occurring carbocyclic ring compounds." Thesis, University of North Bengal, 1989. http://hdl.handle.net/123456789/836.

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Lau, Clifford James. "A study of several interesting carbocyclic molecules /." The Ohio State University, 1987. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487584612166485.

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Books on the topic "Carbocyclic compounds"

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1936-, Ōsawa Eiji, and Yonemitsu Osamu 1930-, eds. Carbocyclic cage compounds: Chemistry and applications. VCH, 1992.

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Carbocycle construction in terpene synthesis. VCH, 1988.

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The chemistry of conjugated cyclic compounds: To be or not to be like benzene? Wiley, 1989.

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E, Osawa, and Yonemitsu O, eds. Carbocyclic Cage Compounds: Chemistry and Applications. VCH Verlagsgesellschaft, Germany, 1992.

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Carbocyclic Three- and Four-membered Ring Compounds. G.Thieme Verlag,Germany, 1996.

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Carbocyclic Three- and Four-membered Ring Compounds. G.Thieme Verlag,Germany, 1997.

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Meijere, Armin De, (Ed.), ed. Carbocyclic Three- and Four-membered Ring Compounds. G.Thieme Verlag,Germany, 1996.

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(Editor), Eiji Osawa, and Osamu Yonemitsu (Editor), eds. Carbocyclic Cage Compounds: Chemistry and Applications (Methods in Stereochemical Analysis). Wiley-VCH, 1992.

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Worakun, Tanachat. Palladium and rhodium catalysed construction of carbocyclic and heterocyclic compounds. 1987.

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Yonemitsu, Osamu. Carbocyclic Cage Compounds: Chemistry and Applications (Methods in Stereochemical Analysis). VCH Publishers, 1992.

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Book chapters on the topic "Carbocyclic compounds"

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Thummel, R. P. "Carbocyclic Annelated Pyridines." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186701.ch2.

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Ninomiya, I., and T. Naito. "Preparation of Carbocyclic Compounds." In Photochemical Synthesis. Elsevier, 1989. http://dx.doi.org/10.1016/b978-0-12-519490-7.50012-8.

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"Substituted Carbocyclic Aromatic Compounds." In Environmental Degradation and Transformation of Organic Chemicals. CRC Press, 2007. http://dx.doi.org/10.1201/9781420006773.ch9.

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"Carbocyclic Aromatic Compounds without Halogen Substituents." In Organic Chemicals in the Environment. CRC Press, 2012. http://dx.doi.org/10.1201/b12492-12.

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"Carbocyclic Aromatic Compounds without Halogen Substituents." In Environmental Degradation and Transformation of Organic Chemicals. CRC Press, 2007. http://dx.doi.org/10.1201/9781420006773.ch8.

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Spitzner, D. "Of Three-Membered Carbocyclic or Heterocyclic Compounds." In Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-00167.

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Spitzner, D. "Of Five-Membered Carbocyclic or Heterocyclic Compounds." In Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-00176.

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"2.1.1. Rearrangement of Homoallylic Compounds." In Carbocyclic Three- and Four-Membered Ring Compounds, edited by Armin de Meijere. Georg Thieme Verlag, 1997. http://dx.doi.org/10.1055/b-0035-113163.

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"Primary Syntheses from Aliphatic or Carbocyclic Synthons." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187975.ch1.

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"3.5. From Cyclopropenes and Metal Carbonyl Compounds." In Carbocyclic Three- and Four-Membered Ring Compounds, edited by Armin de Meijere. Georg Thieme Verlag, 1997. http://dx.doi.org/10.1055/b-0035-112564.

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