Relevant bibliographies by topics / Heterocyclic carbamates and carboxamides

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

Academic literature on the topic 'Heterocyclic carbamates and carboxamides'

Author: Grafiati
Published: 4 June 2021
Last updated: 8 February 2022

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Journal articles on the topic "Heterocyclic carbamates and carboxamides"

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Zaki, Remon Melad, Adel M. Kamal El-Dean, and Shaban M. Radwan. "SYNTHESIS AND REACTIONS OF SOME NEW MORPHOLINYLPYRROLYL TETRAHYDROTHIENO[2,3-c] ISOQUINOLINE." JOURNAL OF ADVANCES IN CHEMISTRY 10, no. 3 (2014): 2512–23. http://dx.doi.org/10.24297/jac.v10i3.6659.

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Hydrazinolysis of ethyl-5-morpholin-4-yl-1-(1H-pyrrol-1-yl)-6,7,8,9-tetrahydrothieno[2,3-c]iso- quinoline-2-carboxylate afforded the corresponding carbo- hydrazide which upon condensation with aromatic aldehydes, acetyl acetone and/ or carbon disulfide gave N- arylidinecarbohydrazide, dimethylpyrazolyl methanone, [1,3,4]oxadiazole-2-thiol and its ethyl ester derivatives respectively. Diazotization of the carbohydrazide with nitrous acid afforded the corresponding carboazide which was used for synthesis of carbamates and substituted carboxamides. Boiling of the carboazide in dry xylene afforded
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Debnath, Pradip. "Recent Advances in the Hofmann Rearrangement and Its Application to Natural Product Synthesis." Current Organic Chemistry 23, no. 22 (2020): 2402–35. http://dx.doi.org/10.2174/1385272823666191021115508.

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: C-N bond formation reactions are the most important transformations in (bio)organic chemistry because of the widespread occurrence of amines in pharmaceuticals, natural products, and biologically active compounds. The Hofmann rearrangement is a well-known method used for the preparation of primary amines from amides. But, the traditional version of the Hofmann rearrangement often gave relatively poor yields due to over-oxidation or due to the poor solubility of some amides in aqueous base, and created an enormous amount of waste products. Developments over the last two decades, in particular
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Aquino, Fabrice, Reinhard Karge, Horst Pauling, and Werner Bonrath. "Dehydration of Aromatic Heterocyclic Carboxamides to Aromatic Heterocyclic Carbonitriles." Molecules 2, no. 12 (1997): 176–79. http://dx.doi.org/10.3390/21100176.

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Brindisi, Margherita, Simone Brogi, Samuele Maramai, et al. "Harnessing the pyrroloquinoxaline scaffold for FAAH and MAGL interaction: definition of the structural determinants for enzyme inhibition." RSC Advances 6, no. 69 (2016): 64651–64. http://dx.doi.org/10.1039/c6ra12524g.

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The pharmacogenic pyrroloquinoxaline scaffold has been exploited for developing piperazine and 4-aminopiperidine carboxamides/carbamates as inhibitors of the endocannabinoids’ catabolic enzymes fatty acid amide hydrolase and monoacylglycerol lipase.
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Qin, Hongbo, Noriyuki Yamagiwa, Shigeki Matsunaga, and Masakatsu Shibasaki. "Bismuth-Catalyzed Intermolecular Hydroamination of 1,3-Dienes with Carbamates, Sulfonamides, and Carboxamides." Journal of the American Chemical Society 128, no. 5 (2006): 1611–14. http://dx.doi.org/10.1021/ja056112d.

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Abdelrazek, Fathy M., Mohamed S. Farghaly, and Hussein E. Abdelrahman. "Synthesis of Some Novel Heterocyclic Xylidinyl Amines and Carboxamides." Journal of Heterocyclic Chemistry 52, no. 1 (2014): 163–68. http://dx.doi.org/10.1002/jhet.1996.

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Wu, Tai Teh, Jamin Huang, Noel D. Arrington, and Gerald M. Dill. "Synthesis and herbicidal activity of .alpha.-heterocyclic carbinol carbamates." Journal of Agricultural and Food Chemistry 35, no. 5 (1987): 817–23. http://dx.doi.org/10.1021/jf00077a044.

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Qin, Hongbo, Noriyuki Yamagiwa, Shigeki Matsunaga, and Masakatsu Shibasaki. "Bismuth- and Hafnium-Catalyzed Hydroamination of Vinyl Arenes with Sulfonamides, Carbamates, and Carboxamides." Chemistry – An Asian Journal 2, no. 1 (2007): 150–54. http://dx.doi.org/10.1002/asia.200600284.

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Norman, Mark H., Frank Navas, James B. Thompson, and Greg C. Rigdon. "Synthesis and Evaluation of Heterocyclic Carboxamides as Potential Antipsychotic Agents." Journal of Medicinal Chemistry 39, no. 24 (1996): 4692–703. http://dx.doi.org/10.1021/jm9603375.

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Lorion, Mélanie M., Julie Oble, and Giovanni Poli. "Palladium catalyzed oxidative aminations and oxylations: where are we?" Pure and Applied Chemistry 88, no. 4 (2016): 381–89. http://dx.doi.org/10.1515/pac-2015-1102.

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AbstractSelective product formation in the Pd-catalyzed cyclization of unsaturated amide and carboxylic acid derivatives is an intriguing and challenging task. We recently discovered that the oxidative intramolecular Pd(II)-catalyzed amination or oxylation of unsaturated N-sulfonyl carbamates, N-sulfonyl carboxamides and carboxylic acids takes place through the involvement of cyclic (usually, 5- or 6-membered) aminopalladated (AmPIs) or oxypalladated (OxPI) intermediates. Such cyclic intermediates can undergo a variety of transformations such as distocyclic β-H elimination, oxidative acetoxyla
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Dissertations / Theses on the topic "Heterocyclic carbamates and carboxamides"

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Verma, Astha. "Small Core Heterocyclic Carbamates and Carboxamides: Resistance-breaking Acetylcholinesterase Inhibitors Targeting the Malaria Mosquito, Anopheles gambiae." Diss., Virginia Tech, 2014. http://hdl.handle.net/10919/64294.

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Malaria is one of the deadliest diseases known to mankind. In 2010, 219 million cases were reported, and 666,000 deaths were attributed to this disease. In the past, pyrethroid-treated mosquito nets have shown efficacy in reducing malaria transmission in many malaria endemic regions. However, an upsurge in the mosquito population that is resistant to pyrethroids threatens to compromise the efficacy of pyrethroid-treated bed nets. In an effort to develop another class of insecticide with a different mode of action, we have explored three classes of five membered heterocyclic carbamates (isoxazo
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Ghavami, Maryam. "Antimalarial Agents: New Mechanisms of Actions for Old and New Drugs." Diss., Virginia Tech, 2018. http://hdl.handle.net/10919/96192.

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Worldwide, malaria is one of the deadliest diseases. In 2016 it sickened 216 million people and caused 445,000 deaths. In order to control the spread of this deadly diseases to human, we can either target the mosquito vector (Anopheles gambiae) or the parasite (Plasmodium falciparum). Due to recent emergence of resistance to current insecticides and antimalarial drugs there is a pressing need to discover and develop new agents that engage new targets in these organisms. To circumvent the effect of resistance to pyrethroid insecticides on the efficacy of insecticide treated nets (ITNs), the us
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Holt, Jarle. "Nitropyridine carbamates, amides and carboxylates in heterocyclic chemistry." Doctoral thesis, Norwegian University of Science and Technology, Department of Chemistry, 2006. http://urn.kb.se/resolve?urn=urn:nbn:no:ntnu:diva-1830.

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<p>Based on new methodology for nitration of pyridine and pyridine derivatives developed at our department by Professor Jan Bakke and coworkers at NTNU, a whole range of substituted nitropyridines are now readily available. The method provides new possibilities in heterocyclic chemistry for the preparation of new materials. Due to the importance and useful properties of many pyridine-based compounds, the chemistry of nitropyridine derivatives is being investigated by our group at NTNU and results for nitropyridine carbamates, amides and carboxylates are presented in this thesis. These nitropyr
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Hlungwani, Isaac. "Design, synthesis and biological evaluation of novel tetrasubstituted quinoline-3-carboxamides derivatives." Diss., 2020. http://hdl.handle.net/11602/1558.

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MSc (Chemistry)<br>Department of Chemistry<br>Quinolines are well known naturally occurring heterocyclic compounds with nitrogen as a heteroatom. Quinolines are also one of the major classes of naturally occurring compounds and the interest in their chemistry is due to the wide range of their biological activities. The objective of the project was the synthesis of novel tetra-substituted quinoline-3carboxamides and subsequent transformation to other novel derivatives and evaluation of their biological activities against malaria and cytotoxicity. In achieving the objective, 2-chloroquinoline-
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Book chapters on the topic "Heterocyclic carbamates and carboxamides"

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Seprõdi, János, Ferenc Hollósy, Dániel Erõs, et al. "HPLC Analysis, Modeling, and Biological Studies of Antiproliferative Heterocyclic Carboxamides." In Peptides: The Wave of the Future. Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-010-0464-0_377.

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"Acylamine or Carbamate and Carboxamide or Nitrile." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187302.ch6.

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"Carbamate or Carboxamide and Another Carboxylic Acid Derivative." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187319.ch62.

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Stratmann, Christian, and Dieter Hoppe. "Stereoselective Intramolecular Cyclization of Nitrogen-substituted Stannylated Alkyl Carbamates." In 19th International Congress on Heterocyclic Chemistry. Elsevier, 2003. http://dx.doi.org/10.1016/b978-0-08-044304-1.50313-0.

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Heydt, H. "Generation of Diazenolates from -{[Alkyl(nitroso)amino]methyl}carboxamides and the Corresponding Carbamates." In Heteroatom Analogues of Aldehydes and Ketones. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-027-00765.

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Kikelj, D. "From 2-Aminophenyl Ketones or 2-Aminobenzaldehydes and Urea, Carbamates, Guanidine, Imidates, or Carboxamides." In Six-Membered Hetarenes with Two Identical Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00769.

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Ivachtchenko, Alexandre V., Vladimir V. Kobak, Alexander V. Khvat, and Caroline Williams. "New Scaffolds for Combinatorial Synthesis and Libraries. New Synthetic Approach to 6-Sulfamoyl-Quinoline-4-Carboxamides." In 19th International Congress on Heterocyclic Chemistry. Elsevier, 2003. http://dx.doi.org/10.1016/b978-0-08-044304-1.50197-0.

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Conference papers on the topic "Heterocyclic carbamates and carboxamides"

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STADLBAUER, Wolfgang, and Corinna MOSER. "Synthesis of Heterocyclic Carbamates with Potential Activity in Plant Protection." In The 17th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-a027.

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Journal articles
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