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Relevant bibliographies by topics / Oxazinanes

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Journal articles
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Academic literature on the topic 'Oxazinanes'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Oxazinanes"

1

Van Nguyen, Tuyen, Matthias D’hooghe, Hang Dao Thi, Giang Le Nhat Thuy, Saron Catak, and Veronique Van Speybroeck. "Use of 3-Hydroxy-4-(trifluoromethyl)azetidin-2-ones as Building Blocks for the Preparation of Trifluoromethyl-Containing Aminopropanes, 1,3-Oxazinan-2-ones, Aziridines, and 1,4-Dioxan-2-ones." Synthesis 50, no. 07 (2018): 1439–56. http://dx.doi.org/10.1055/s-0036-1591537.

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3-Hydroxy-4-(trifluoromethyl)azetidin-2-ones were synthesized from the corresponding 3-benzyloxy-β-lactams and successfully transformed into new 3-chloro-4-(trifluoromethyl)azetidin-2-one building blocks. The latter chlorides were shown to be eligible precursors for the construction of CF3-containing aminopropanes, 1,3-oxazinanes, 1,3-oxazinan-2-ones, and aziridines. In addition, 3-hydroxy-4-(trifluoromethyl)azetidin-2-ones proved to be interesting substrates for the synthesis of novel 3-[2,2,2-trifluoro-1-(arylamino)ethyl]-1,4-dioxan-2-ones via intramolecular cyclization of 3-(2-hydroxyethoxy

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2

Chandgude, Ajay L., Daniele Narducci, Katarzyna Kurpiewska, Justyna Kalinowska-Tłuścik, and Alexander Dömling. "Diastereoselective one pot five-component reaction toward 4-(tetrazole)-1,3-oxazinanes." RSC Adv. 7, no. 79 (2017): 49995–98. http://dx.doi.org/10.1039/c7ra07392e.

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3

Hardman, Andrea M., Sonia S. So, and Anita E. Mattson. "Urea-catalyzed construction of oxazinanes." Organic & Biomolecular Chemistry 11, no. 35 (2013): 5793. http://dx.doi.org/10.1039/c3ob41517a.

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4

Cheng, Shuanghua, and Shouyun Yu. "Enantioselective synthesis of 3-substituted 1,2-oxazinanes via organocatalytic intramolecular aza-Michael addition." Org. Biomol. Chem. 12, no. 43 (2014): 8607–10. http://dx.doi.org/10.1039/c4ob01646g.

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A highly enantioselective intramolecular 6-exo-trig aza-Michael addition was developed to afford chiral 3-substituted 1,2-oxazinanes in high yields (up to 99% yield) and good enantioselectivities (up to 98/2 er).

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5

Zhai, Pingan, Wenhui Li, Jianying Lin, Shuangping Huang, Wenchao Gao, and Xing Li. "N-Alkyl nitrones as substrates for access to N-aryl isoxazolidines via a catalyst-free one-pot three-component reaction with nitroso compounds and olefins." Organic Chemistry Frontiers 8, no. 14 (2021): 3752–59. http://dx.doi.org/10.1039/d1qo00398d.

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N-Alkyl nitrones are used as starting materials to construct N-aryl isoxazolidines, instead of N-alkyl isoxazolidines or N–H 1,3-oxazinanes via a catalyst-free one-pot three-component reaction with nitrosoarenes and olefins.

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6

Vukićević, Rastko, Matthias D’hooghe, Anka Pejović, et al. "Synthesis and Antimicrobial/Cytotoxic Assessment of Ferrocenyl Oxazinanes, Oxazinan-2-ones, and Tetrahydropyrimidin-2-ones." Synlett 26, no. 09 (2015): 1195–200. http://dx.doi.org/10.1055/s-0034-1380348.

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7

Hardman, Andrea M., Sonia S. So, and Anita E. Mattson. "ChemInform Abstract: Urea-Catalyzed Construction of Oxazinanes." ChemInform 45, no. 2 (2013): no. http://dx.doi.org/10.1002/chin.201402172.

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8

Zanatta, Nilo, Adriana M. C. Squizani, Leonardo Fantinel, et al. "Synthesis of N-substituted 6-trifluoromethyl-1,3-oxazinanes." Journal of the Brazilian Chemical Society 16, no. 6a (2005): 1255–61. http://dx.doi.org/10.1590/s0103-50532005000700025.

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9

Van Nguyen, Tuyen, Matthias D’hooghe, Hang Dao Thi та ін. "Synthesis of Trifluoromethylated Azetidines, Aminopropanes, 1,3-Oxazinanes, and 1,3-Oxazinan-2-ones Starting from 4-Trifluoromethyl-β-lactam Building Blocks". Synlett 27, № 07 (2016): 1100–1105. http://dx.doi.org/10.1055/s-0035-1561316.

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10

Singh, Kamajit, and Prasant K. Deb. "A Versatile Approach to trans-1,3-Disubstituted Tetrahydro-b-carbolines Using Oxazinanes." HETEROCYCLES 51, no. 7 (1999): 1509. http://dx.doi.org/10.3987/com-99-8580.

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More sources

Dissertations / Theses on the topic "Oxazinanes"

1

Baldwin, Andrea Michelle. "Synthesis and Functionalization of Heterocycles via Non-Covalent Catalysis." The Ohio State University, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=osu1467277822.

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2

Nimmagadda, Sri Krishna. "Asymmetric Transformations Catalyzed By Chiral BINOL Alkaline Earth Metal Phosphate Complexes." Scholar Commons, 2016. http://scholarcommons.usf.edu/etd/6554.

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Small molecule hydrogen bond donors have emerged as versatile catalysts in asymmetric synthesis. Within this class, chiral BINOL phosphoric acid is regarded as one of the pioneer catalysts used in several asymmetric transformations. The ability of the catalyst to activate the substrates could be controlled in two different ways. (1) Dual activation/bifunctional activation of substrate by hydrogen bond interactions or ion pairing with phosphoric acid or (2) By forming chiral BINOL phosphate metal complex that could significantly alter the interactions in chiral space. In particular, chiral alka

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3

Ella-Menye, Jean-Rene. "Synthesis of Novel Chiral Heterocyclic Compounds for Antibacterial Agents and Peptidomimetics." ScholarWorks@UNO, 2007. http://scholarworks.uno.edu/td/611.

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Small chiral molecules are very important building blocks in the synthesis of biologically active compounds. These building blocks include nitrogen and oxygen-containing heterocycles such as 2-oxazolidinones, 1,3-oxazinan-2-ones, 2-oxazolines, oxazines, morpholine and morpholinones. Because of their interesting properties, chiral heterocycles have stirred great interest in the synthetic chemist community to develop useful and efficient strategies to these molecules. In this dissertation, the design and syntheses of various heterocyclic building blocks are presented, as well as the testing of t

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4

Khankischpur, Mehdi [Verfasser]. "4-funktionalisierte 1,3-Oxazinan-2-one, N'-Alkyliden-3-hydroxy-propanhydrazonamide und β-Hydroxy-hydrazonate [Beta-Hydroxy-hydrazonate] als Leitstrukturen neuer antiparasitärer Wirkstoffe : Synthese, Analytik und Bestimmung der biologischen Aktivität gegenüber Plasmodium falciparum / vorgelegt von Mehdi Khankischpur". 2009. http://d-nb.info/995301425/34.

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