Relevant bibliographies by topics / Aminocyclohexanol

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Aminocyclohexanol'

Author: Grafiati
Published: 4 June 2021
Last updated: 14 February 2022

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Journal articles on the topic "Aminocyclohexanol"

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Kläui, Wolfgang, Susanne Schoger, and Martin Nieger. "Synthese und Kristallstruktur von Perhydro-1,4-benzoxazino[2,3-n]phenoxazin/Synthesis and Crystal Structure of Perhydro-1,4-benzoxazino[2,3-n]phenoxazine." Zeitschrift für Naturforschung B 52, no. 7 (1997): 801–4. http://dx.doi.org/10.1515/znb-1997-0706.

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Abstract The oxidation of trans-2-aminocyclohexanol with nitrobenzene in the presence of catalytic amounts of iron inter alia yields perhydro-1,4-benzoxazino[2,3-n]phenoxazine (1). This compound has been characterized analytically, spectroscopically and by X-ray diffraction. It is postulated that the oxidation of the 2-aminoalcohol leads to the intermediate formation of a 1,2-dione. The direct synthesis of 1 from trans-2-aminocyclohexanol and 1,2-cyclohexandione supports this hypothesis.
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Bernardelli, Patrick, Michael Bladon, Edwige Lorthiois, Ajith C. Manage, Fabrice Vergne, and Roger Wrigglesworth. "Resolution of trans-3-aminocyclohexanol." Tetrahedron: Asymmetry 15, no. 9 (2004): 1451–55. http://dx.doi.org/10.1016/j.tetasy.2004.03.034.

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Chinnakali, K., H. K. Fun, K. Sriraghavan, and V. T. Ramakrishnan. "N-(4-Nitrophenyl)-trans-2-aminocyclohexanol." Acta Crystallographica Section C Crystal Structure Communications 53, no. 12 (1997): 1865–67. http://dx.doi.org/10.1107/s0108270197010159.

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Bolm, C., I. Schiffers, T. Rantanen, F. Schmidt, W. Bergmans, and L. Zani. "Resolution of 2-Aminocyclohexanol Derivatives and Applications." Synfacts 2006, no. 6 (2006): 0589. http://dx.doi.org/10.1055/s-2006-934464.

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Samoshin, Vyacheslav V., Yu Zheng, and Xin Liu. "Trans -2-Aminocyclohexanol derivatives as pH-triggered conformational switches." Journal of Physical Organic Chemistry 30, no. 11 (2017): e3689. http://dx.doi.org/10.1002/poc.3689.

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Luna, Amparo, Covadonga Astorga, Ferenc Fülöp, and Vicente Gotor. "Enzymatic resolution of (±)-cis-2-aminocyclopentanol and (±)-cis-2-aminocyclohexanol." Tetrahedron: Asymmetry 9, no. 24 (1998): 4483–87. http://dx.doi.org/10.1016/s0957-4166(98)00482-0.

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Maestro, Alicia, Covadonga Astorga, and Vicente Gotor. "Enzymatic resolution of (±)-trans-2-aminocyclohexanol and (±)-trans-2-aminocyclopentanol." Tetrahedron: Asymmetry 8, no. 18 (1997): 3153–59. http://dx.doi.org/10.1016/s0957-4166(97)00368-6.

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Chatterjee, A., M. Sasikumar,, and N. N. Joshi. "Preparation of Enantiopure trans‐1,2‐Cyclohexanediol and trans‐2‐Aminocyclohexanol." Synthetic Communications 37, no. 10 (2007): 1727–33. http://dx.doi.org/10.1080/00397910701266075.

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Kidwai, Mazaahir, Bhavesh Dave, and Seema Kohli. "ChemInform Abstract: Synthesis of Novel Oxaziridines Derived from trans-4-Aminocyclohexanol." ChemInform 30, no. 46 (2010): no. http://dx.doi.org/10.1002/chin.199946116.

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Rebollo, Oscar, Esther del Olmo, Grace Ruiz, José L. López-Pérez, Alberto Giménez, and Arturo San Feliciano. "Leishmanicidal and trypanocidal activities of 2-aminocyclohexanol and 1,2-cyclohexanediamine derivatives." Bioorganic & Medicinal Chemistry Letters 18, no. 1 (2008): 184–87. http://dx.doi.org/10.1016/j.bmcl.2007.10.102.

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Dissertations / Theses on the topic "Aminocyclohexanol"

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Zhang, Ningrong. "Trans-2-aminocyclohexanol as a pH-sensitive conformation switch in liposomes." Scholarly Commons, 2007. https://scholarlycommons.pacific.edu/uop_etds/681.

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Acid-sensitive liposome has drawn much interest as drug and gene carriers that release payloads specifically at the low-pH target sites, such as in solid tumors, tissues with inflammation, and ischemia sites. Also, it helps drug/gene to escape endosome trapping and followed lysosome degradation. The goal of this thesis research is to develop novel trans-2-aminocyclohexanols based lipids and their liposome that can be switched by mildly acidic pH. NMR study · show that in certain acidic medium, the amine group on cyclohexane will attract proton and form hydrogen bond with the neighboring -OH. T
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Liu, Xin. "Fliposomes: pH-sensitive liposomes comprising novel trans-2-aminocyclohexanol-based amphiphiles as conformational switches for the liposome mebrane." Scholarly Commons, 2013. https://scholarlycommons.pacific.edu/uop_etds/149.

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As a promising pH-triggerable molecular switch, trans -2-aminocyclohexanol (TACH) has a variety of applications. By introducing two hydrocarbon tails, multiple TACH-based lipids (flipids) have been designed and studied that are able to perform a drastic conformational flip upon protonation, loosening the stacking of hydrocarbon tails in lipid bilayers. Liposomes constructed from such flipids (fliposomes) can be disrupted by this acid-triggered conformational flip to cause a rapid release of a cargo specifically in areas of increased acidity (such as inflammation or ischemic tissues, solid tumo
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Zheng, Yu. "Synthesis and conformational study of trans-2-aminocyclohexanol-based pH-triggered molecular switches and their application in gene delivery." Scholarly Commons, 2013. https://scholarlycommons.pacific.edu/uop_etds/153.

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Trans-2-Aminocyclohexanol (TACH) is a promising model for pH-triggerable molecular switches with a variety of potential applications. In particular, such a switch, when incorporated into cationic liposomes, provides a novel design of the pH-sensitive helper lipids for gene delivery. Protonation of TACH molecules results in a strong intramolecular hydrogen bond between the amino and its neighboring hydroxyl groups, which triggers a conformational flip, and forces changes of the relative position of other substituents on the ring. In this work, a library of TACH-lipids has been designed and buil
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Sviatenko, Olha [Verfasser], Matthias [Akademischer Betreuer] Höhne, Matthias [Gutachter] Höhne, and García Iván [Gutachter] Lavandera. "Combining ketoreductase and amine transaminase for 4-aminocyclohexanol synthesis / Olha Sviatenko ; Gutachter: Matthias Höhne, Iván Lavandera García ; Betreuer: Matthias Höhne." Greifswald : Universität Greifswald, 2020. http://d-nb.info/1224047427/34.

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Amoozadeh, Ali. "Photochemical rearrangement of 2-phenylthio-3-aminocyclohexanols, new access to deoxyazasugars and their derivatives." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape3/PQDD_0025/NQ52123.pdf.

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Book chapters on the topic "Aminocyclohexanol"

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Szammer, János, Zoltán Banka, József Margitfalvi, Sándor G_bölös, and Zoltán Tóth. "Highly Selective Preparation of trans-4-Aminocyclohexane Carboxylic Acid from cis-Isomer over Raney® Nickel Catalyst." In Catalysis of Organic Reactions. CRC Press, 2006. http://dx.doi.org/10.1201/9781420007794.ch6.

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