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Relevant bibliographies by topics / Cavitando chirale

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Journal articles

Academic literature on the topic 'Cavitando chirale'

Author: Grafiati

Published: 11 March 2023

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Journal articles on the topic "Cavitando chirale"

1

Mann, Enrique, and Julius Rebek. "Deepened chiral cavitands." Tetrahedron 64, no. 36 (2008): 8484–87. http://dx.doi.org/10.1016/j.tet.2008.05.136.

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2

Irwin, Jacob L., David J. Sinclair, Alison J. Edwards, and Michael S. Sherburn. "Chiral Conjoined Cavitands." Australian Journal of Chemistry 57, no. 4 (2004): 339. http://dx.doi.org/10.1071/ch03299.

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Tetrabromocavitand bowls are converted into rim-connected hexabromodimers in one step in 17–22% yields by oxidative coupling of higher order arylcuprates. 1H NMR and single crystal X-ray analyses of the rim-connected dimers reveal a conformationally restricted structure in which the rims of the two cavitand bowls describe planes angled at 78.8° to one another. Each of the two bowl cavities are occupied by a guest, in addition to being partially occluded by a portion of the complementary bowl rim. These new host compounds exhibit a very unusual form of enantioisomerism.

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3

Martín Carmona, María Antonia. "Natural and synthetic cavitands: challenges in chemistry and pharmaceutical technology." Anales de la Real Academia Nacional de Farmacia 87, no. 87(04) (2021): 381–94. http://dx.doi.org/10.53519/analesranf.2021.87.04.02.

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Supramolecular chemistry involves non-covalent interactions and specific molecular recognition of molecules/analytes by host molecules or supramolecules. These events are present in synthesis, catalysis, chiral separations, design of sensors, cell signaling processes and drug transport by carriers. The typical behavior of supramolecules is derived from their ability to build well-structured self-assembled and self-organized entities. Cavitands are a particular group of supramolecules possessing a cavity able to include a variety of compounds thanks to host-guest non-covalent interactions devel

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4

Stefanelli, Manuela, Donato Monti, Valeria Van Axel Castelli, et al. "Chiral supramolecular capsule by ligand promoted self-assembly of resorcinarene-Zn porphyrin conjugate." Journal of Porphyrins and Phthalocyanines 12, no. 12 (2008): 1279–88. http://dx.doi.org/10.1142/s1088424608000662.

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Cavitand- Zn porphyrin conjugates self-assemble to give supramolecular (1 + 1) structures upon coordination of bifunctional ligands such as 4,4'-bipyridine and the like. The formation of the capsule depends on key structural factors, such as the size of the cavity, and the possibility of the onset of hydrogen bonds, π–π and π–cation interactions. The extension of this protocol to chiral bifunctional ligands, such as (+)-cinchonine and (−)-cinchonidine, and cinchona alkaloid derivatives, results in the achievement of supramolecular structures with chiral cavities, whose configuration is depende

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5

Desai, Arpita S., Thennati Rajamannar, and Shailesh R. Shah. "Molecular Container and Metal Ion Sensor Chiral Cavitands." ChemistrySelect 5, no. 34 (2020): 10588–92. http://dx.doi.org/10.1002/slct.202002273.

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6

Li, Na, Fan Yang, Hillary A. Stock, David V. Dearden, John D. Lamb, and Roger G. Harrison. "Resorcinarene-based cavitands with chiral amino acid substituents for chiral amine recognition." Organic & Biomolecular Chemistry 10, no. 36 (2012): 7392. http://dx.doi.org/10.1039/c2ob25613d.

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7

Inoue, Mami, Yoshino Fujii, Yasuhiro Matsumoto, Michael P. Schramm, and Tetsuo Iwasawa. "Inherently Chiral Cavitand Curvature: Diastereoselective Oxidation of Tethered Allylsilanes." European Journal of Organic Chemistry 2019, no. 34 (2019): 5862–74. http://dx.doi.org/10.1002/ejoc.201900891.

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8

D'Urso, Alessandro, Cristina Tudisco, Francesco P. Ballistreri, et al. "Enantioselective extraction mediated by a chiral cavitand–salen covalently assembled on a porous silicon surface." Chem. Commun. 50, no. 39 (2014): 4993–96. http://dx.doi.org/10.1039/c4cc00034j.

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9

Nishimura, Ryo, Ryo Yasutake, Shota Yamada, et al. "Chiral metal nanoparticles encapsulated by a chiral phosphine cavitand with the tetrakis-BINAP moiety: their remarkable stability toward ligand exchange and thermal racemization." Dalton Transactions 45, no. 11 (2016): 4486–90. http://dx.doi.org/10.1039/c5dt04660b.

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A chiral phosphine cavitand1induced the formation of chiral metal (Ru, Rh, Pd, Ag, Pt, and Au) nanoparticles (NPs). The ligand1of the chiral metal NPs prevents both thermal racemization and ligand exchange with a thiol.

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10

Maffei, Francesca, Giovanna Brancatelli, Tahnie Barboza, Enrico Dalcanale, Silvano Geremia, and Roberta Pinalli. "Inherently chiral phosphonate cavitands as enantioselective receptors for mono-methylated L-amino acids." Supramolecular Chemistry 30, no. 7 (2017): 600–609. http://dx.doi.org/10.1080/10610278.2017.1417991.

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