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Dissertations / Theses on the topic 'Furan derivatives'

Author: Grafiati

Published: 4 June 2021

Last updated: 26 July 2025

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1

Yazicioglu, Emre Yusuf. "Transformation Of Cyclohexanone Derivatives To Bicyclic Furan And Pyrrole Derivatives." Master's thesis, METU, 2004. http://etd.lib.metu.edu.tr/upload/12605269/index.pdf.

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Tetrahydrobenzofurans and tetrahydroindoles are two very valuable classes of substances which have wide usage area<br>either as starting materials for drug substances or many other compounds which have fused heterocyclic rings in their structures and pharmacophore for many complex natural products<br>syntheses of derivatives of these compounds with different substitution patterns, is an exciting challenge for many scientists. Benzofuran and tetrahydroindole derivatives, which are potent bioactive substances, are synthesized from various cyclohexanone derivatives that are allylated by Stork-ena

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2

Livi, Francesco. "From 3,3,4,4-Tetraethoxybut-1-yne to furan derivatives." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2012. http://amslaurea.unibo.it/3004/.

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The starting material for this project was the highly functionalized compound 3,3,4,4- tetraethoxybut-1-yne (TEB) and it can be prepared from ethyl vinyl ether by a 4-steps synthesis. The third and the fourth step in TEB synthesis were sensitive to reaction conditions, so it was developed a strategy to try to optimize the third step and obtain TEB with higher yields. An approach, which tries to optimize also the fourth step, will be developed in further works. Several γ-hydroxy-α,β-unsaturated acetylenic ketones can be prepared from 3,3,4,4- tetraethoxybut-1-yne. TEB and γ-hydroxy-α,β-un

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3

Woollaston, Daniel. "Total synthesis of natural products via the oxidation of furan derivatives." Thesis, University of Oxford, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.491599.

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Oxidation of furan rings in the presence of hydroxy groups can lead to spirobutenolides. This methodology has been applied in synthetic studies towards three natural products: Pyrenolide 0 - An antileukaemic fungal metabolite. AL-(1) - An antitumor plant natural product. Sawaranospirolides - Four highly oxygenated spiroacetals isolated from the heartwood of the Sawara tree.

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4

Gowda, Anitha Shankaralinge. "HYDROGENATION AND HYDROGENOLYSIS OF FURAN DERIVATIVES USING BIPYRIDINE-BASED ELECTROPHILIC RUTHENIUM(II) CATALYSTS." UKnowledge, 2013. http://uknowledge.uky.edu/chemistry_etds/29.

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The catalytic activity of ruthenium(II) bis(diimine) complexes cis-[Ru(6,6′-Cl2bpy)2(OH2)2](Z)2 (2, Z = CF3SO3; 3, Z = (3,5-(CF3)2C6H3)4B ,i.e. BArF), cis-[Ru(4,4′-Cl2bpy)2(OH2)2](Z)2 (4, Z = CF3SO3; 5, Z = BArF) and cis-[Ru(bpy)2(PR3)(OH2)](CF3SO3)2 (7, bpy = 2,2’-bipyridine, PR3 = P(C6H4F)3; 8, bpy = 2,2-bipyridine, PR3 = PPh3; 9, bpy = 4,4’-dichloro-2,2’-bipyridine, PR3 = PPh3; 10, bpy = 4,4’-dimethyl-2,2’-bipyridine, PR3 = P(C6H4F)3) for the hydrogenation and hydrogenolysis of furfural (FFR), furfuryl alcohol (FFA) and 5-hydroxymethylfurfural (HMF) was investigated. The compounds 2-5 are a

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5

Raffa, Guillaume. "Hétérocyclisations électrophiles et pallado-catalysées d’α-alcynyl β-alcoxyénones (et systèmes apparentés) : nouvelles voies d’accès à des dérivés furaniques tétrasubstitués". Thesis, Lyon 1, 2011. http://www.theses.fr/2011LYO10236.

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6

Banert, Klaus, Sandra Bochmann, Andreas Ihle, et al. "Synthesis with Perfect Atom Economy: Generation of Furan Derivatives by 1,3-Dipolar Cycloaddition of Acetylenedicarboxylates at Cyclooctynes." Universitätsbibliothek Chemnitz, 2014. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-qucosa-152891.

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Cyclooctyne and cycloocten-5-yne undergo, at room temperature, a 1,3-dipolar cycloaddition with dialkyl acetylenedicarboxylates 1a,b to generate furan-derived short-lived intermediates 2, which can be trapped by two additional equivalents of 1a,b or alternatively by methanol, phenol, water or aldehydes to yield polycyclic products 3b–d, orthoesters 4a–c, ketones 5 or epoxides 6a,b, respectively. Treatment of bis(trimethylsilyl) acetylenedicarboxylate (1c) with cyclooctyne leads to the ketone 7 via retro-Brook rearrangement of the dipolar intermediate 2c. In all cases, the products are formed w

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7

Weber, Isabelle Kathrin [Verfasser], and M. [Akademischer Betreuer] Olzmann. "Kinetic Studies with Shock Tubes: Instrumental Developments and the Thermal Decomposition of Furan Derivatives / Isabelle Kathrin Weber ; Betreuer: M. Olzmann." Karlsruhe : KIT-Bibliothek, 2018. http://d-nb.info/1166234312/34.

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8

Hartmann, Ana Paula. "Síntese e avaliação de derivados furânicos, tetraidrofurânicos e pirrólicos com potencial atividade tripanocida." Universidade de São Paulo, 2015. http://www.teses.usp.br/teses/disponiveis/60/60138/tde-25092015-113957/.

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A Doença de Chagas é causada pelo Trypanosoma cruzi, e possui duas fases clínicas, sendo o tratamento com o fármaco benznidazol eficaz somente na fase aguda, porém com diversos efeitos adversos ao longo do período do tratamento. Desta forma, consórcios vêm sendo estabelecidos entre \"governo - universidade - indústria\", com auxilio de capital nacional e estrangeiro para o desenvolvimento de novos fármacos. Apesar de diversas ferramentas disponíveis para o planejamento de novos compostos, a busca por produtos naturais ainda desperta interesse de muitos pesquisadores. Diversos trabalhos vêm des

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9

Ulbrich, Kathrin [Verfasser], and Oliver [Akademischer Betreuer] Reiser. "The conversion of furan derivatives from renewable resources into valuable building blocks and their application in synthetic chemistry / Kathrin Ulbrich. Betreuer: Oliver Reiser." Regensburg : Universitätsbibliothek Regensburg, 2014. http://d-nb.info/1068055839/34.

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10

Benahmed-Gasmi, Amina. "Nouveaux précurseurs de matériaux organiques conducteurs : des donneurs-pi aux polymères conjugués." Angers, 1996. http://www.theses.fr/1996ANGE0020.

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Ce travail porte sur l'élaboration et la caractérisation de plusieurs séries de systèmes hybrides du tetrathiafulvalène (HTTFS). Ces systèmes sont construits par le greffage de deux motifs 1,3-dithiole-2-ylidene aux deux extrémités d'un espaceur conjugué. Apres une première étape consacrée à l'analyse des différentes possibilités d'insertion d'espaceurs benzéniques, plusieurs séries de HTTFS dérivées d'hétérocycles aromatiques, thiophène, furanne et n-méthyl pyrrole, ont été synthétisées, l'analyse des propriétés électrochimiques de ces derniers montre qu'ils conduisent à un abaissement du pot

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11

Fernandez, Anne-Marie. "Préparation de γ-butyrolactones γ-alkylées optiquement pures à partir de l'acide L-tartrique. Application à la synthèse totale de la L-bioptérine". Rouen, 1996. http://www.theses.fr/1996ROUES025.

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Une nouvelle méthode pour la préparation de gamma-butyrolactones optiquement pures est proposée. Une stratégie de synthèse donnant accès à deux types de chirons carbonylés (cétones et aldéhyde) a permis le développement de deux réactions hautement stéréosélectives créant ainsi un troisième centre stéréogénique : la réduction des cétones, (2R, 3R)-2,3-dipivaloxy-4-oxo alcanoates de méthyle par le borohydure de sodium dans le méthanol mène aux alcools correspondants (4R), avec des ee>98%, précurseurs des (2R,3S,4R)-2,3-dipivaloxy-4-alkylbutyrolactones. L'addition d'organomagnésiens sur l'aldéhyd

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12

Lenoir, Jean-Yves. "Préparation de furannes 2,3,5-trisubstitués par métallations régiosélectives de 2-furyloxazolines. Application à la synthèse de produits naturels." Rouen, 1994. http://www.theses.fr/1994ROUES027.

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Ce travail décrit la préparation de furannes 2,3,5-trisubstitués à partir de 2-furyloxazolines par métallations régiosélectives des sommets 3 et 5 du furanne. Nous avons également étudié la métallation des chaînes latérales en position 5 de (5-alkyl-2-furyl)oxazolines. Les résultats obtenus ont permis la synthèse d'un monoterpènoïde d'origine naturelle: le 5-isobutyl-3-méthylfurfural. Nous proposons une nouvelle approche pour la synthèse de précurseurs potentiels de composés furanniques macrocycliques de type pseudoptérane

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13

Ericsson, Cecilia. "Synthesis of Tetrahydrofuran and Pyrrolidine Derivatives Utilising Radical Reactions : Organochalcogenides in Reductive, Carbonylative and Group-Transfer Cyclisation." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis : Univ.-bibl. [distributör], 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-4018.

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14

Goussé, Cécile. "Applications de la réaction de Diels-Alder aux polymères furaniques." Grenoble INPG, 1997. http://www.theses.fr/1997INPG0007.

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Certains derives furaniques, obtenus a partir de la biomasse, se comportent comme d'excellents dienes vis a vis de la reaction de diels-alder. Dans cette perspective, l'application de cette reaction aux polymeres furaniques peut etre envisagee sous deux aspects. Le premier consiste en la modification de polymeres tels l'alcool polyvinylique ou le polystyrene par greffage de groupements pendants furaniques, qui seront ensuite mis en reaction avec des mono ou bismaleimides conduisant respectivement a des polyadduits ou des gels. Le second concerne la synthese et la polycondensation de monomeres

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15

Azevedo, Mariangela Burgos Martins de. "Synthèse énantiosélective de (gamma)-butyrolactones : ()-méthylénolactocine, (-)-acide protolichestérinique, (-)-blastmycinolactol, (+)-blastmycinone, (-)-NFX-2 et (+)-antimycinone." Université Joseph Fourier (Grenoble ; 1971-2015), 1995. http://www.theses.fr/1995GRE10116.

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La cycloaddition du dichlorocetene avec des éthers d'enols chiraux conduit à des cyclobutanones fonctionnalisées avec une diastéréosélectivité élevée. Cette réaction est basée sur la différenciation des faces de la double liaison de l'oléfine chirale. Des intermédiaires de pureté enantiomerique élevée, comme les gamma-butyrolactones, sont obtenus à partir des cycloadduits. Au cours de ce travail, nous avons effectué les premières synthèses enantioselectives des produits naturels suivants: la (moins)-methylenolactocine et l'(moins)-acide protolichesterinique. Ces alpha-méthylène-gamma-butyrolac

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16

Egunlusi, Ayodeji Olatunde. "Novel tricycloundecane derivatives as potential N-methyl-Daspartate receptor and calcium channel inhibitors for neuroprotection." Thesis, University of the Western Cape, 2014. http://hdl.handle.net/11394/3904.

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>Magister Scientiae - MSc<br>This study focused on the synthesis of a series of novel tricycloundecane derivatives and evaluation of these compounds for neuroprotection using the fluorescent ratiometric calcium assay that indicates the ability of the test compounds to inhibit NMDA receptors and VGCC. The cycloaddition reaction between p-benzoquinone and monomerised dicyclopentadiene yielded tricycloundeca- 4,9-diene-3,6-dione which was used as the base structure and further derivatised. These derivatives were conjugated with benzylamine to form a series of imines and amines. A total of 10 comp

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17

Coutterez, Claire. "Synthèse, caractérisation et étude des propriétés d'oligomères et polymères hétéroarylène vinylènes." Grenoble INPG, 1998. http://www.theses.fr/1998INPG0163.

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Le travail de cette these a concerne la synthese, la caracterisation et l'etude de proprietes d'usage de structures oligomeres et polymeres conjuguees. L'originalite de ces travaux reside d'une part dans l'utilisation d'heterocycles furaniques et thiopheniques comme elements constitutifs des chaines et d'autre part, dans le fait que de nombreux composes oligomeres ont ete cibles, isoles et caracterises. Les possibilites d'application de ces materiaux dans les domaines touchant a l'electronique (conducteurs ou semi-conducteurs), a l'optique (cristaux liquides) et a la luminescence photo- et ele

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18

Signoret, Christian. "Réseaux polyuréthannes classiques et contenant des motifs furanniques pour le confinement de déchets radioactifs : relations structure-propriétés." Grenoble INPG, 1989. http://www.theses.fr/1989INPG0088.

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Etude des proprietes mecaniques, de la stabilite thermique de la diffusion de l'eau et de sels radioactifs dans des polyurethannes. Les polyetherurethannes souples ont un comportement moyen a la temperature et a la diffusion. Les polyesterurethannes ont un meilleur comportement mais sont hydrolyses rapidement les polyetherurethannes rigides (tv=20 a 40#oc) sont le meilleur compromis; amelioration de la tenue en temperature vers 350-500#oc par addition de derives furanniques

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19

Wu, Jin-Ti, and 吳進益. "Study on Photochemistry of Furan and Thiophene Derivatives." Thesis, 1999. http://ndltd.ncl.edu.tw/handle/54640388557788524634.

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博士<br>國立臺灣大學<br>化學研究所<br>87<br>A novel photochemical rearrangement of this work is from a series of 2-(4’-alkylstyryl)furan or thiophene to 5-(3-alkylbutadienyl)benzo[b]-furan or thiophene with good yields. The starting materials were prepared from 2-furaldehyde and the corresponding benzyl chloride or bromide using Wittig reaction, the UV absorption is at 330 nm. The styrylfuran or styrylthiophene is known to undergo photochemical isomerization and in the presence of oxygen or iodine to afford cyclized products, but the skeletal rearrangement is occurred only when photolysis is carried out in

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20

Chih-Ming, Chou, and 周志明. "Synthesis of 2,3,5-trisubstituted Furan Derivatives from Propargylic Dithioacetals." Thesis, 2003. http://ndltd.ncl.edu.tw/handle/01013212437679536581.

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碩士<br>國立臺灣大學<br>化學研究所<br>91<br>It has recently been reported in our group a new annulation approach to synthesis of 2,3,5-trisubstituted furans from the corresponding propargylic dithioacetals and aldehydes. Encouraged by this study, we introduced an ester group into the terminal alkyne of propargylic dithioacetal. After annulation, we successfully synthesized a variety of 3-ester-group-substituted furan derivatives. Reaction of progargylic dithioacetals with dialdehydes or trialdehyde afforded a series of bis-furans and C3 symmetry star-shape furan derivatives, respectively. Photop

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21

Su, Yih-Chen, and 蘇益辰. "Pyrolytic Study of 2-azidomethylbenzo[b]furan and its Derivatives." Thesis, 1998. http://ndltd.ncl.edu.tw/handle/77610793714143448868.

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22

Cheng, Pai Chung, and 白宗城. "Enantiocontrolled Construction of Tricyclic Furan Derivatives via An Asymmetric Diels Alder Reaction." Thesis, 2001. http://ndltd.ncl.edu.tw/handle/56208372100748395294.

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23

Lee, Tzu-Cheng, and 李子誠. "Systematic Studies of Diazodicarbonyl Compounds-reaction with Furan Derivatives and Heterocycles Synthesis." Thesis, 2018. http://ndltd.ncl.edu.tw/handle/69hnyb.

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碩士<br>國立中山大學<br>化學系研究所<br>106<br>Furan and derivatives can undergo versatile reactions, including electrophilic addition, [2+1] or [4+3] cycloaddition, or ring-opening by acids. In 1990, Prof. Wenkert use furan with ethyl diazoacetate to synthesize furan ring-opening diene compound through carbenoid-furan ring-opening. In the last decades, a lots of studies in furan derivatives reacting with carbenoid had been published. This thesis is the first study utilizing methodology way to investigate the reactions and products of acceptor/acceptor type dicarbonyl carbenoid reacting with furan derivativ

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24

Data, Przemysław. "Electrochemical and spectroelectrochemical investigation of phenylenevinylene derivatives with furan, thiophene, selenophene and tellurophene substituents." Rozprawa doktorska, 2012. https://repolis.bg.polsl.pl/dlibra/docmetadata?showContent=true&id=4179.

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25

Data, Przemysław. "Electrochemical and spectroelectrochemical investigation of phenylenevinylene derivatives with furan, thiophene, selenophene and tellurophene substituents." Rozprawa doktorska, 2012. https://delibra.bg.polsl.pl/dlibra/docmetadata?showContent=true&id=4179.

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26

Chang, Chia-Lin, and 張嘉麟. "Synthesis and Biological Activity of Ethyl 5-(2'-Alkoxycarbonyl substituted phenoxy)furan-2-carboxylate Derivatives." Thesis, 2002. http://ndltd.ncl.edu.tw/handle/75686963187553654926.

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博士<br>中國醫藥學院<br>藥物化學研究所<br>90<br>A series of ethyl 5-(2'-alkoxycarbonyl substituted phenoxy)furan-2-carboxylate derivatives has been synthesized and identified. All of these synthetic compounds were evaluated for antiplatelet aggregation, anti-allergic and anti-inflammatory activities. In synthesis, CsF promoted the esterification of salicylic acids to give substituted salicylic acid methyl ester (2-4 and 6-13). Ethyl 5-nitro-2-furoate (14) was synthesized by the nitration reaction from ethyl furoate with fuming nitric acid. Ethyl 5-(2'-alkoxycarbonyl substituted phenoxy)furan-2-car

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27

Liao, Ying-Chi, and 廖英錡. "Pyrolytic Study of 2-(2-Vinylstyryl)furan derivatives and 2-[2-(4-Methoxyphenyl)vinyl]benzo[b]thiophene." Thesis, 2006. http://ndltd.ncl.edu.tw/handle/32400694735627980679.

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碩士<br>國立中山大學<br>化學系研究所<br>94<br>Flash vacuum pyrolysis of 2-(2-vinylstyryl)furan derivatives via electrocyclization followed by dehydrogenation will give 2-(2-naphthalen-2-yl)furan analogues, on the other hand, FVP of 2-(2-vinylstyryl)furan derivatives via electrocyclization followed by [1,5]-H shift will give 3-(2-furyl)-1,2-dihydronaphthalene analogues. FVP of 2-[2-(4-methoxyphenyl)vinyl]benzo[b]thiophene gave three products: trans-4-(2-benzo[b]thiophen-2-ylvinyl)phenol, benzo[b]naphtha[1,2-d]thiophen-2-ol and 1H-6-thiacyclopenta[c]fluorene.

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28

Shieh, Po-Chuen, and 謝博銓. "Metal Carbenoid Ring Opening of 2-alkyl and Alkoxy Furan-Synthesis, Application and SAR of 1,6-Dioxo-2,4-diene Derivatives." Thesis, 2001. http://ndltd.ncl.edu.tw/handle/20644773906736288350.

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博士<br>國立中山大學<br>化學系研究所<br>89<br>Abstract 2-Methoxy- and 2-trimethylsilyloxyfuran undergo facile ring opening reaction upon treatment with metal carbeniod. Treatment of 2-methoxy-furan with ethyl diazoacetate and aryl-α-diazocarbonyl compounds under metal catalysis afford (Z,E)-2,4-hexadienedioate and aryl-6-oxo-2,4-hexadienoates respectively. When 2- trimethylsilyloxyfuran was used, desilylation occurred to give directly the monoprotected (Z,E)-muconic acid and 6-aryl-6-oxo-2,4-hexadienoic acids. We have synthesized aromatic dienyl diketone using the method of Wenkert from aromatic diazo

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29

Huang, Zheng-Shan, and 黃丁山. "The syntheses of azulene derivatives by the reaction of 2H-cyclohepta [ b ] furan-2-ones with vinyl ether and vinyl acetates." Thesis, 1986. http://ndltd.ncl.edu.tw/handle/72142215866384143423.

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30

Lai, Chun-Chia, and 賴俊嘉. "Density Functional Theory study of [8+2] and [4+2] Cycloaddition Reactions of 2-Oxo-2H-cyclohepta[b]furan derivatives with Dienes." Thesis, 2002. http://ndltd.ncl.edu.tw/handle/80744404394630730734.

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碩士<br>國立彰化師範大學<br>化學系<br>90<br>Abstract Cycloaddition reactions of 2-Oxo-2H-cyclohepta[b]furan derivates participating as 8π and 4π components respectively toward dienes are described. We use density functional theory (DFT) calculations in the study of transition states and products of title reactions. Possible [4+2] and [8+2] reaction paths were investigated. Our results show that Part 1: [8+2] endo path, is the most likely both thermodynamically and kinetically. The distinct selectivity of the [8+2] endo path over the [4+2] endo one was explained in terms of the secondary orbital

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31

陳筱鳳. "Gold(I)-Catalyzed Intramolecular Cyclization of 1-Aryl-2-(3-arylpropargyl)cyclohex-2-en-1-ols: Synthesis of Tetrahydrobenzo[b]furan Derivatives." Thesis, 2014. http://ndltd.ncl.edu.tw/handle/kppe53.

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碩士<br>國立臺灣師範大學<br>化學系<br>102<br>The thesis discusses chloro(triphenylphosphine)gold(I) (Ph3PAuCl) and silver trifluoromethanesulfonate (AgOTf) cocatalyzed intramolecular cycloisomerization of 1-arylcyclohex-2-en-1-ols bearing an alkynylalkyl tether at the C-2 position of the ring. Treatment of 1-aryl-2-(3-arylpropargyl)cyclohex-2-en-1-ols with a catalytic amount of Ph3PAuCl/AgOTf at room temperature under nitrogen in minutes provided tetrahydrobenzo[b]furan derivatives in good yields. This reaction can be expanded to an alkyl substitution at the tertiary carbinol carbon and the terminal alkyn

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32

李得响. "The syntheses of azulene derivatives by the reaction of 3,5-disubstituted 2H-cyclohepta [ b ] furan-2-ones with vinyl ethers and vinyl acetates." Thesis, 1987. http://ndltd.ncl.edu.tw/handle/52065934201600858651.

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33

Liu, Chien-Liang, and 劉健良. "The study in copper(II) chloride-mediated one pot three-step syntheses of benzo[b]furan derivatives and its application for the total synthesis of antimicrobial molecular." Thesis, 2012. http://ndltd.ncl.edu.tw/handle/03492873832870849922.

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碩士<br>國立中興大學<br>化學系所<br>100<br>Copper(II) chloride has been successfully used as the medium to one-pot three-steps synthesis of benzo[b]furan derivatives. A palladium-free and ligand-free reaction condition for Sonogashira- type coupling has been developed, this catalytic system is cheap and easily removed, and provide a good yield. Total synthesis of antimicrobial molecule was accomplished in six steps. This novel route was starting from the 4-methylanisole 64. The iodination of compound 64 by treating with NIS in the presence of TMSCl can provide the 90% yield. After the copper(II) chloride

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34

CHEN, KE-LUN, and 陳克倫. "Intermolecular & intramolecular reactions of furans with enedione derivatives." Thesis, 1990. http://ndltd.ncl.edu.tw/handle/29623492301008156522.

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35

"Part I. The chemistry of a planar cyclooctatetraene derivative fused to phenanthrene ring: and Part II. Regiospecific synthesis of 2,3-disubstituted and 2,3,5-trisubstituted furans from 2,4-bis(trimethylsilyl)furan." Chinese University of Hong Kong, 1993. http://library.cuhk.edu.hk/record=b5887840.

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by Chun-yip Leung.<br>Thesis (M.Phil.)--Chinese University of Hong Kong, 1993.<br>Includes bibliographical references (leaves 72-76).<br>Acknowledgements --- p.1<br>Chapter Part 1). --- The Chemistry of A Planar Cyclooctatetraene Derivatives Fused to Phenanthrene Ring --- p.2<br>Chapter (I). --- Abstract --- p.2<br>Chapter (II). --- Introduction --- p.3<br>Chapter (III). --- Results and Discussion --- p.9<br>Chapter (IV). --- Conclusion --- p.18<br>Chapter (V). --- Experimental Section --- p.19<br>Chapter Part 2). --- "Regiospecific Synthesis of 2,3-Disubstituted and 2,3,5-Trisubstitute

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XIE, HUAN-JIA, and 謝煥佳. "Oxidation of cyclopenladiene derivatives and furans with PCC,and its synthetic applications." Thesis, 1988. http://ndltd.ncl.edu.tw/handle/72900619763521543234.

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Lin, Zhu-Qiang, and 林助強. "Oxidation of cyclopentadiene derivatives and furans with PCC, and its synthetic applications." Thesis, 1988. http://ndltd.ncl.edu.tw/handle/71182763486756890880.

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Hsieh, Meng-Hsuan, and 謝孟諠. "Copper Catalyst for the Synthesis of Various Aryl Amido Furans and Hydroxyisoindolinone Derivatives." Thesis, 2016. http://ndltd.ncl.edu.tw/handle/38331170882723849787.

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碩士<br>國立臺灣師範大學<br>化學系<br>104<br>The contents of thesis is mainly divided into two chapters and further, each chapter individually included preamble, research goal, results description and conclusion. In the first chapter, deals with a copper catalyzed tandem Sonogashira coupling reaction and cycloisomerization for the synthesis of trisubstituted furans derivative from 2-iodo-N- phenylbenzamide derivative and 3-propargyl-1,3-diketone in the presence of copper iodide and cesium carbonate mild conditions, moderate to good yields, rapid reactions are important features of this methodology. The sec

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WANG, FANG-YU, and 王方宇. "Derivatives of thiophene、furane、pyrrol、pyridine, studies of synthesis and their coordination with cobalt (II) perchlorate." Thesis, 1989. http://ndltd.ncl.edu.tw/handle/31816823005608550623.

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