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Dissertations / Theses on the topic '2-Amino alcohol'

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Published: 4 June 2021
Last updated: 13 February 2022

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1

Fattori, Juliana. "Sintese de 2-amino-3, 5-diois." [s.n.], 2007. http://repositorio.unicamp.br/jspui/handle/REPOSIP/248461.

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Orientador: Luiz Carlos Dias<br>Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Quimica<br>Made available in DSpace on 2018-08-10T02:46:17Z (GMT). No. of bitstreams: 1 Fattori_Juliana_M.pdf: 2240885 bytes, checksum: 9db38d985e4bc4fb6668aeb311352757 (MD5) Previous issue date: 2007<br>Resumo: A unidade aminodiol está presente em esfingolipídeos que são uma importante classe de biomoléculas. Os esfingolipídeos são componentes das membranas celulares e estão relacionados a processos de crescimento, diferenciação celular e apoptose. Alguns esfingolipídeos como a esfingosi
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2

Gunler, Zeynep Inci. "Synthesis Of N-(2-propylphenyl) Substituted Chiral Amino Alcohols And Their Usage In Enantioselective Diethylzinc Addition Reactions." Master's thesis, METU, 2011. http://etd.lib.metu.edu.tr/upload/12613001/index.pdf.

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Chiral 1,2-amino alcohols were synthesized via newly developed &ldquo<br>intramolecular unsaturation transfer&rdquo<br>using cyclohexanone, propargyl bromide, and various chiral amino alcohols as starting components. These amino alcohols can be potential chiral ligands for many asymmetric transformation reactions. Therefore, their effectiveness as chiral ligands in diethylzinc addition to benzaldehyde and N-diphenylphosphinoyl imines were tested. Various parameters including temperature, solvent, ligand amount etc. were screened for the synthesized chiral ligands. In diethylzinc addition to be
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3

Zaid, Abdelhamid. "Préparation et activité pharmacologique de l'anisyl-5 triméthyl-1,9,9 oxa-3 aza-4 bicyclo [4. 2. 1] nonane et de ses dérivés amino-acylés." Montpellier 1, 1987. http://www.theses.fr/1987MON13514.

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4

Sehl, Torsten [Verfasser], Martina [Akademischer Betreuer] Pohl, and Jörg [Akademischer Betreuer] Pietruszka. "2-Steps in 1-pot: enzyme cascades for the synthesis of chiral vicinal amino alcohols / Torsten Sehl. Gutachter: Martina Pohl ; Jörg Pietruszka." Düsseldorf : Universitäts- und Landesbibliothek der Heinrich-Heine-Universität Düsseldorf, 2014. http://d-nb.info/1051734681/34.

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5

Pinho, Pedro. "Development and application of new chiral -amino alcohols in synthesis and catalysis : Use of 2-azanorboryl-3-methanols as common intermediates in synthesis and catalysis." Doctoral thesis, Uppsala universitet, Kemiska institutionen, 2001. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-1267.

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The development and application of unnatural amino alcohols,prepared via hetero-Diels-Alder reactions,in synthesis and catalysis is described.The studies are concerned with the [i]scope of the hetero-Diels-Alder reaction and preparation of important intermediates in the synthesis of antiviral agents,[ii ]application of amino alcohols in the ruthenium transfer hydrogenation of ketones,[iii ]use of similar precursors in the in situ generation of oxazaborolidines for reduction of ketones,and [iv] development and application of new chiral auxiliaries for dialkylzinc additions to activated imines,
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6

Renaud, Jean-Paul. "Oxydations d'alcanes et d'alcènes par des systèmes métalloporphyriniques modelés du cytochrome P-450." Paris 6, 1986. http://www.theses.fr/1986PA066139.

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La synthèse d'une pophyrine de fer à "anses de panier" chirale comportant des aminoacidés de configuration déterminée est décrite. On a étudié sa pureté optique et sa conformation en solution. Dans une deuxième partie on décrit un nouveau système oxydant catalytique utilisant l'eau oxygénée en présence d'une porphyrine de manganèse et d'imidazole permettant la conversion quantitative d'alcènes en époxydes et d'alcanes en alcools et cétones.
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7

Guignard, Alain. "Emploi de la cyano-2 cyclopentanone comme agent de blocage de la fonction aminé : synthèse d'amino-alcools optiquemment actifs, application à la préparation d'oxazolines chirales." Tours, 1986. http://www.theses.fr/1986TOUR4001.

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Synthèse de béta -aminoalcools (à fonction : amine primaire et alcool tertiaire) à partir de la réaction de l'oxo-2 cyclopentanecarbonitrile avec des esters d'aminoacides. Synthèse d'homologues de la (-)norephédrine optiquement actifs. à partir des béta -aminoalcools, synthèse d'oxazolines-2 (i). étude de la réaction de meyers sur les composés (i)
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8

Guignard, Alain. "Emploi de la cyano-2 cyclopentanone comme agent de blocage de la fonction amine, synthèse d'amino-alcools optiquement actifs application à la préparation d'oxazolines chirales." Grenoble 2 : ANRT, 1986. http://catalogue.bnf.fr/ark:/12148/cb37598106b.

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9

Reinaud, Olivia. "Nouvelles methodes d'alkylation regioselective d'orthoquinones originales : synthese de differentes classes de produits naturels quinoniques." Paris 6, 1987. http://www.theses.fr/1987PA066200.

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10

Henze, Rüdiger. "Tautomérisation énantiosélective d'un énol." Rouen, 1997. http://www.theses.fr/1997ROUES020.

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La réaction de l'aldéhyde 2-benzylacrylique avec des acides thiocarboxyliques donne accès à de nouveaux énols métastables. Leur conformation a été étudiée en utilisant des calculs semi-empiriques et des méthodes spectroscopiques. Des calculs AM1 ont révélé que la conformation préférée du Z-éthanethioate de 2-benzyl-3-hydroxy-2-propényle en absence de solvants fait intervenir une interaction intramoléculaire entre les groupements hydroxyle et carbonyle du thioester. Une étude par IR et par RMN a montré que la conformation du Z-1-benzènecarbothioate de 2-benzyl-3-hydroxy-2-propényle était dépend
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11

Amadji, Morad. "Catalyse asymétrique à l'aide d'alcoolates chiraux : synthèse de chirons en série 1,3-dioxanes." Rouen, 1997. http://www.theses.fr/1997ROUES011.

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La nature du groupement en position 2 des 2-alkyl ou 2-aryl-5-méthylène-1,3-dioxanes permet d'accéder exclusivement à un seul isomère dibromo-1,3-dioxane Cis ou Trans correspondant. La déshydrohalogénation énantiosélective, à l'aide d'alcoolate de la N-méthyléphédrine, des composés dibromo-1,3-dioxanes Trans conduit à de très hautes séléctivités (ee>98%) en particulier lorsque le substituant en position 2 est un groupement aryle. Une version catalytique, performante et novatrice, de la déshydrohalogénation énantiosélective, par un système relais mettant en jeu une quantité catalytique de métha
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12

Shieh, Chyuan-Jaqn, and 謝全展. "Reactioms of 2-chloride-5-nitrobenzensulfonic acid with aromatic alcohol, aromatic amine." Thesis, 1999. http://ndltd.ncl.edu.tw/handle/61464022228774001880.

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碩士<br>國立中央大學<br>化學工程研究所<br>87<br>Benzidine and it's derivatives were identified that they would let the maker and user got cancer recently, so they were forbidden to use in the world. This proposal is going to study the reactions of 2-chloride-5-nitrobenzensulfonic acid (abbreviated to "CNBS") with aromatic alcohol and CNBS with aromatic amine. The products of the reactions may offer people another choice about producing and using intermediate of dyes. There are three products of CNBS with aromatic alcohol. They are 2-phenoxy-5-nitro-benzensulfonic acid { IR(cm-1) : 1520, 1350 (N-O) }, 2-(4'-a
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13

Chen, Jia Chong, and 陳家重. "1.HPLC separation of enantiomers of amino acids and amino alcohols. 2.Separation of pyridine related compounds and copper corrosion inhibitors by capillary electrophoresis." Thesis, 1995. http://ndltd.ncl.edu.tw/handle/20795617005681559994.

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博士<br>國立臺灣大學<br>化學研究所<br>83<br>A. Part I Six silica-based ionically bonded chiral stationary phases consisting of cyanuric chloride with substituents an L-amino acid and a dialkylamine were prepared. These phases provide recognition ability to separate enantiomers of both methyl esters of N-(3,5-dinitrobenzoyl)-amino acids and N-(3,5-dinitrobenzoyl)-amino alcohols in high-performance liquid chromatographys. Generally, amino acids were separated more effectively than amino alcohols. A mechanism for chiral
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14

Lin, Cheng-Kun, та 林正坤. "The Studies on New Synthetic Methodologies:1. Asymmetric Synthesis of α-Methyl-α-Amino Acids via Diastereoselective Alkylation of (1S)-(+)-3-Carene-derived Tricyclic Iminolactone2. A Simple Method for the Oxidation of Primary Alcohols with 2-Iodoxybenzo". Thesis, 2011. http://ndltd.ncl.edu.tw/handle/70513668306709259121.

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博士<br>中興大學<br>化學系所<br>99<br>1. Asymmetric Synthesis of α-Methyl-α-Amino Acids via Diastereoselective Alkylation of (1S)-(+)-3-Carene-derived Tricyclic Iminolactone Either proteinogenic or nonproteinogenic α-amino acids play very important roles in many fields. Due to the importance of α-amino acids, numerous efficient methods for their asymmetric synthesis have been growing rapidly. Although these methods can provide good yields and enantiomeric excesses of α-amino acids, some of them suffered from requiring the use of strong bases under low temperatures or resulting in poor or no recovery o
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15

Trinh, Nguyen Thu Thao. "Synthèse diastétéosélective de motifs 4-amino-3-hydroxy-2-méthylpentanoate de méthyle via une séquence impliquant une aldolisation de Mukaiyama et une réduction radicalaire à partir de dérivés d'acides [alpha]-aminés." Thèse, 2005. http://hdl.handle.net/1866/16776.

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