Relevant bibliographies by topics / Cyclopenta-1

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers
  5. Reports

Academic literature on the topic 'Cyclopenta-1'

Author: Grafiati
Published: 4 June 2021
Last updated: 2 February 2022

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Journal articles on the topic "Cyclopenta-1"

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Campbell, M., DJ Collins, and AM James. "Synthesis of 2-(5',5'-Ethylenedioxy-1'-methylcyclopent-2'-en-1'-yl)ethanol, and Some 2H-Cyclopenta[b]furan Derivatives Formed by Intramolecular Displacement Reactions." Australian Journal of Chemistry 42, no. 1 (1989): 17. http://dx.doi.org/10.1071/ch9890017.

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Exchange dioxolanation of 2-methyl-2-(prop-2′-enyl)cyclopentane-1,3-done (1b) gave 3,3- ethylenedioxy-2-methyl-2-(prop-2′-enyl) cyclopentan-1-one (2) which, upon reduction and esterification , afforded the epimeric 3,3-ethylenedioxy-2-methyl-2-(prop-2′-enyl) cyclopent-1-yl benzoates (6d). Oxidative cleavage of the terminal double bond in (6d),followed by sodium borohydride reduction yielded 3,3-ethylenedioxy-2-(2'-hydroxyethyl)-2-methylcyclopent-1-yl benzoate (4b) which underwent acid- catalysed rearrangement to 6a-(2′-hydroxyethoxy)-3a- methylhexahydrocyclopenta [b]furan-4-yl benzoate (8b). Flash vacuum pyrolysis of the t- butyldimethylsilyl ether (12), derived from the hydroxy acetal (4b), afforded 3-[2′- (t- butyldimethylsilyloxy )ethyl]-4,4-ethy1enedioxy-3-methylcyclopent-1-ene (14) which upon selective cleavage of the silyl ether group gave 2-(5′,5′-ethylenedioxy-1′-methylcyclopent- 2'′en-1′-y1)ethanol (7). Reaction of the mesylate (16) of (7) with lithium bromide or iodide in tetrahydrofuran at 50-55� for several hours yielded some of the corresponding 3-(2′-haloethyl) compounds (17), but gave mainly the rearranged 6a-(2′-haloethoxy)-3a-methyl-3,3a,6,6a-tetrahydro-2H-cyclopenta[b]furans (19a) and (19b). Some related chemistry is described.
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Gataullin, Rail R., Ekaterina S. Mescheryakova, Rifkat M. Sultanov, Akhnef A. Fatykhov, and Leonard M. Khalilov. "An Unexpected Dihalogenation/Dehydrogenation Product Derived­ via Iodolactonization of an N-Tosyl-N-[6-(2-cyclopenten-1-yl)-2-methylphenyl]glycine." Synthesis 51, no. 18 (June 19, 2019): 3485–90. http://dx.doi.org/10.1055/s-0039-1689971.

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The reaction between N-tosyl-N-[6-(2-cyclopenten-1-yl)phenyl]glycine (syn/anti atropisomeric mixture) and molecular iodine is studied. Along with the expected 8-exo-cyclization product possessing a 3-iodo-2,3,3a,6,7,11b-hexahydrobenzo[e]cyclopenta[g][1,4]oxazocine core, the unexpected 1,11b-dehydrogenated/1-iodinated analogue with a 1,3-diiodo-3,3a,6,7-tetrahydrobenzo[e]cyclopenta[g][1,4]oxazocine structure is observed for the first time in a conventional halolactonization reaction.
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Kotha, Sambasivarao, and Yellaiah Tangella. "Modular Approaches to Cyclopentanoids and their Heteroanalogs." Synlett 31, no. 20 (October 12, 2020): 1976–2012. http://dx.doi.org/10.1055/a-1288-8240.

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AbstractCyclopentanoids and their derivatives are interesting targets in synthetic organic chemistry due to their extensive applications in various branches of chemical sciences like pharmaceuticals, natural and non-natural products. In view of these applications, several synthetic strategies have been developed in the past three to four decades. In this article, we describe our work towards the synthesis of cyclopentanoids and their heteroanalogs involving diverse synthetic strategies during the past two decades. Among these, photo-thermal olefin metathesis, ring-closing metathesis, ring-rearrangement metathesis, cyclopentane annulation, [2+2+2] cycloaddition and Diels–Alder reactions have been used to assemble cyclopentane rings of diverse architecture. 1 Introduction 2 Synthesis of Spiro[4.4]nonane (A1) Derivatives 3 Synthesis of Octahydropentalene (A2) Derivatives 4 Synthesis of Linear Triquinanes (A3) 5 Synthesis Spiro Triquinanes (A4) 6 Synthesis of Angular Triquinane (A5) Systems 7 Synthesis of Hexahydro-2′H-spiro[cyclopentane-1,1′-pentalene] (A6) Ring System 8 Synthesis of Dispiro[4.1.47.25]tridecane (A7) Ring System 9 Synthesis of Hexahydro-1H-3a,7a-propanoindene Ring System10 Synthesis of Linear Tetraquinanes (A11 and A12)11 Synthesis of Tetrahydro-1′H,3′H-dispiro[cyclopentane-1,2′-pentalene-5′,1′′-cyclopentane] (A13) Ring System12 Synthesis of Decahydro-1H,8H-dicyclopenta[a,h]pentalene (A14) Ring System13 Synthesis of Dodecahydro-1H-dicyclopenta[a,d]pentalene (A15) Ring System14 Synthesis of Octahydro-1′H-spiro[cyclopentane-1,2′-cyclopenta[c]pentalene] (A16) Ring System15 Synthesis of Decahydrospiro[cyclopentane-1,7′-cyclopenta-[a]pentalene] (A17) Ring System16 Synthesis of Compact Tetraquinane (A18)17 Synthesis of Higher Polyquinanes18 Conclusions19 Acronyms
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Si, Mrinal Kanti, and Bishwajit Ganguly. "A DFT study to design super- and hyperacids with 1-(cyclopenta-2,4-dien-1-yl)-4-nitrobenzene and 3-(cyclopenta-2,4-dien-1-ylmethylene)-6-methylenecyclohexa-1,4-diene molecules." New Journal of Chemistry 41, no. 4 (2017): 1425–29. http://dx.doi.org/10.1039/c6nj03529a.

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DFT calculations reveal that poly-cyano-substituted 1-(cyclopenta-2,4-dien-1-yl)-4-nitrobenzene and 3-(cyclopenta-2,4-dien-1-ylmethylene)-6-methylenecyclohexa-1,4-diene can function as super- to hyper-acids.
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Peipiņš, Uldis, Niks Freimanis, Dmitrijs Stepanovs, Anatoly Mishnev, and Māris Turks. "Betulin 3,28-di-O-tosylate." Acta Crystallographica Section E Structure Reports Online 70, no. 8 (July 23, 2014): o879—o880. http://dx.doi.org/10.1107/s1600536814016602.

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The title compound, C44H62O6S2{systematic name: (1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-3a-[(tosyloxy)methyl]icosahydro-1H-cyclopenta[a]chrysen-9-yl 4-methylbenzenesulfonate}, was obtained by tosylation of naturally occurring betulin. All the cyclohexane rings adopt chair conformations and the cyclopentane ring adopts a twisted envelope conformation, with the C atom bearing the tosylmethyl substituent forming the flap. In the crystal, molecules form a three-dimensional network through multiple weak C—H...O hydrogen bonds.
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Çelik, Ísmail, Mehmet Akkurt, Ahmet Tutar, Ramazan Erenler, and Santiago García-Granda. "2,3-Dihydro-1H-cyclopenta[b]naphthalen-1-ol." Acta Crystallographica Section E Structure Reports Online 68, no. 3 (February 10, 2012): o687. http://dx.doi.org/10.1107/s1600536812005181.

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Wardakhan, Wagnat Wahba, El-Sayed Nahed Nasser Eid, and Rafat Milad Mohareb. "Synthesis and anti-tumor evaluation of novel hydrazide and hydrazide-hydrazone derivatives." Acta Pharmaceutica 63, no. 1 (March 1, 2013): 45–57. http://dx.doi.org/10.2478/acph-2013-0004.

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The reaction of cyclopentanone with cyanoacetylhydrazine gave 2-cyano-2-cyclopentylideneacetohydrazide (1). Treatment of compound 1 with elemental sulphur in the presence of triethylamine afforded 2-amino-5,6-dihydro- -4H-cyclopenta[b]thiophene-3-carbohydrazide (2), which in-turn formed the corresponding intermediate diazonium salt. The latter was coupled with either ethyl cyanoacetate or ethyl acetoacetate to form 2-cyano-2-(3-(hydrazinecarbonyl)- 5,6-dihydro-4H-cyclopenta[b]thiophen-2-yl)hydrazono) acetate (3) and ethyl 2-(2-(3-(hydrazinecarbonyl)-5,6-dihydro- 4H-cyclopenta[b]thiophen-2-yl)hydrazono)-3-oxobutanoate (4), respectively. On the other hand, the reaction of compound 1 with either benzaldehyde or acetophenone afforded N’-benzylidene-2-cyano-2-cyclopentylideneacetohydrazide (7) and 2-cyano-2-(2-cyclopentylidene)phenylacetohydrazide (10), respectively. Moreover, compound 1 was used to synthesize 2-cyano-2-cyclopentylidene- N'-(arylthiazol-2(3H)-ylidene)acetohydrazides (6a,b), 2-(2-benzylidenecyclopentylidene)-2-cyanoacetohydrazide (8), 2-amino-N'-benzylidene-5,6-dihydro-4H- -cyclopenta[b]thiophene-3-carbohydrazide (9), 2-cyano- -2-(2-(2-phenylhydrazono)cyclopentylidene)acetohydrazide (11), N'-(1-chloropropan-2-ylidene)-2-cyano-2-cyclopentylideneacetohydrazide (12), and 2-cyclopentylidene-3- -(3,5-disubstituted-1H-pyrazol-1-yl)-3-oxopropanenitriles (13a,b) through its reaction with the respective reagents. Antitumor evaluation of the newly synthesized compounds against the three human tumor cells lines, namely, breast adenocarcinoma (MCF-7), non-small cell lung cancer (NCI-H460) and CNS cancer (SF-268) showed that some of the described compounds exhibited higher inhibitory effects towards the three tumor cell lines than the reference compound doxorubicin.
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Gelbrich, Thomas, Volker Kahlenberg, Christoph Langes, and Ulrich J. Griesser. "Telaprevir: helical chains based on three-point hydrogen-bond connections." Acta Crystallographica Section C Crystal Structure Communications 69, no. 2 (January 16, 2013): 179–82. http://dx.doi.org/10.1107/s0108270113000954.

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The crystal structure of the title compound [systematic name: (1S,3aR,6aS)-2-((2S)-2-{[(2S)-2-cyclohexyl-2-(pyrazine-2-carbonylamino)acetyl]amino}-3,3-dimethylbutanoyl)-N-[(3S)-1-(cyclopropylamino)-1,2-dioxohexan-3-yl]-3,3a,4,5,6,6a-hexahydro-1H-cyclopenta[c]pyrrole-1-carboxamide], C36H53N7O6, contains two independent molecules, which possess distinct conformations and a disordered cyclopenta[c]pyrrolidine unit. In the crystal, molecules are linked into helical chainsviathree-point N—H...O hydrogen-bond connections in which three NH and three carbonyl groups per molecule are utilized. The chiralities of the six stereocentres per molecule inferred from this study are in agreement with the synthetic procedure.
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Christensen, Torben Bo, Karl Anker Jørgensen, Finn Krebs Larsen, Lars Martiny, Jørgen Møller, Alexander Senning, and Lucia Vichi. "Formation of a 4H-cyclopenta-1,2,3-thiadiazole by rearrangement of a transient N-(thionitroso)cyclopenta-2,4-diene-1-imine." J. Chem. Soc., Chem. Commun., no. 6 (1993): 489–91. http://dx.doi.org/10.1039/c39930000489.

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Huo, Fang-Jun, Cai-Xia Yin, and Pin Yang. "7-Nitro-2,3-dihydro-1H-cyclopenta[b]chromen-1-one." Acta Crystallographica Section E Structure Reports Online 60, no. 11 (October 22, 2004): o2087—o2089. http://dx.doi.org/10.1107/s1600536804026078.

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Dissertations / Theses on the topic "Cyclopenta-1"

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Grandin, Anna. "Synthetic Routes towards 2-thia-7,8-diaza-cyclopenta[l]phenanthrene and 1-thia-7,8-diaza-cyclopenta[l]phenanthrene for Molecular Electronics Applications." Thesis, Mälardalens högskola, Akademin för hållbar samhälls- och teknikutveckling, 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:mdh:diva-7505.

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Electric current is known to flow through the π-bonds in oligothiophenes. In order to use them as molecular wires it is important to use a technique where the potential gradients can be generated and maintained in supramolecular networks. A solution to this problem can be the use of metal complexes as junction points within such a network.  In this project pathways to synthesize 2-thia-7,8-diaza-cyclopenta[l]phenanthrene (1) and 1-thia-7,8-diaza-cyclopenta[l]phenanthrene (2) for use in molecular electronic devices have been investigated. 4-(5-Bromo-thiophen-2-yl)2,2’-bipyridine (3) was prepared via Kröhnke reaction from 3-(5-bromothiophene-2-yl)acrolein and 1-(2-Oxo-2-pyridine-2-yl-ethyl)-pyridinium iodide in an overall yield of 14 %.    Several routes towards 2-thia-7,8-diaza-cyclopenta[l]phenanthrene (1) and 1-thia-7,8-diaza-cyclopenta[l]phenanthrene (2) were tested. Since the original planned pathway did not work, lack of time made it impossible to complete the series of experiments that were needed. The synthesis of 2-thia-7,8-diaza-cyclopenta[l]phenanthrene (1) is almost finished. Due to the solvation problems, after the decarboxylation step, the product could not be analyzed by 1H-NMR in a satisfactory manner. The product was sent for analysis.  A number of experiments towards 1-thia-7,8-diaza-cyclopenta[l]phenanthrene (2) were tested but few of them worked as planned. There is a lot of work left to be done in the synthesis of this compound but the lack of time made it impossible.  The chemistry that has been achieved is the synthesis of 1,10-phenanthroline-5,6-dione in the synthesis of 2-thia-7,8-diaza-cyclopenta[l]phenanthrene (1). The following Hinsberg thiophene synthesis probably worked but due to solvation problems the product could not be isolated. The final product after hydrolysis and decarboxylation of the remaining ester groups after the Hinsberg thiophene synthesis was tested but the results were difficult to confirm.  In the synthesis of 1-thia-7,8-diaza-cyclopenta[l]phenanthrene (2) several attempts to make 3,4-diamino-N,N-diethyl-benzamide were made. The attack from the primary amines on the carbonyl carbon made it necessary to protect them. The attempt to synthesize 3,4-bis-acetylamino-N,N-diethyl-benzamide also failed, both the attempt directly from the carboxylic acid and through the acylchloride, even though the amines were protected.
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Dallemagne, Patrick. "Synthèse et étude de la réactivité chimique des premiers amino-4 cyclopenta[b] thiophènes ; application aux nouvelles séries de l'amino-3 indanone-1 et de l'amino-6 cyclopenta[b] thiophène." Caen, 1988. http://www.theses.fr/1988CAEN4071.

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Nadarajah, Sivakumar. "Synthesis and reactions of a 2-cyclopenten-1-one d³ synthon." Thesis, University of British Columbia, 1986. http://hdl.handle.net/2429/26010.

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This thesis describes the preparation of 3-trimethylstannyl-2-cyclo-penten-1-one 14 via the higher order stannylcuprate 78, a new reagent prepared to convert 3-iodo-2-cyclopenten-1-one 75 to the desired product. The observations made from this chemistry led to the development of "one-pot" cuprate formation which was demonstrated to be a viable and practically convenient way to generate such species compared with traditional methods. This thesis also describes the preparation of 3-tert-butyldimethyl-siloxy-1-trimethylstannylcyclopentene 83, its conversion into the corresponding lithio species, and reaction of the latter reagent with electrophiles. Thus, transmetalation of 83 with methyllithium produced 1—lithio— 3-tert-butyldimethylsiloxycyclopentene 84, which reacted smoothly at -78°C in tetrahydrofuran with alkyI halides, aldehydes, and ketones, providing the corresponding products in good yield. Treatment of the vinyllithium reagent 84 with 1 equiv. of phenylthiocopper or cuprous cyanide at -78° C for 1 h gave solutions of the corresponding cuprate reagents 103 and 104, respectively. Similarly the corresponding Grignard reagent 105 was made by addition of 1 equiv. of magnesium bromide to the solution of 84 at -78°C. The reagents thus produced reacted in a conjugate sense, the latter catalyzed by copper (I) bromide-dimethylsulphide complex, to enones such as 2-cyclopenten-1-one and 2-cyclohexen-l-one, affording the corresponding products 106 and 107 in excellent yields. β-lodo enones such as 3-iodo-2-cyclopenten-1-one 75 and 3-iodo-2-cyclohexen-1-one 7 also reacted with the cuprate 103 in a conjugate sense to give the corresponding products 108 and 109 in excellent yields. The cyanocuprate 104 prepared by a "one-pot" process also reacted with 3-iodo-2-cyclopenten-1-one 75 to give the enone 108 in good yield. [See Thesis For Diagrams]
Science, Faculty of
Chemistry, Department of
Graduate
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Perrard, Thierry. "Synthèse énantiosélective des énantiomères du dihydrojasmonate de méthyle." Rouen, 1999. http://www.theses.fr/1999ROUES054.

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Dans la première partie de ce travail, nous avons imaginé un projet de synthèse du (+)-dihydroépijasmonate de méthyle, un composé ayant des propriétés odorantes intéressantes dans lequel l'étape-clef est un dédoublement cinétique par des amidures de magnésium chiraux dans une réaction de déprotonation régiosélective. Nous avons suivi ce projet jusqu'à la synthèse du dihydrojasmonate de méthyle racémique de configuration trans. Des essais de protonation diastéréosélective et des essais de cis-hydrogénation n'ont pas donné le dihydroépijasmonate de méthyle pur de configuration cis désiré. Ce composé s'épimérise très facilement en dihydrojasmonate de méthyle de configuration trans plus stable. Parallèlement à cette synthèse, nous avons essayé de trouver de nouvelles applications aux amidures de magnésium chiraux, réactifs peu utilisés en synthèse organique. Nous avons tenté des carboxylations électrophiles sur des intermédiaires azaalylmagnésium, issus de la déprotonation d'imines prochirales par des amidures de magnésium. Nous n'avons pas isolé le chlorhydrate d'aminoester voulu, les amidures de magnésium ne semblent pas être adaptés à ce type de conditions expérimentales. Dans la deuxième partie de ce travail, nous avons mis au point une nouvelle méthode de synthèse en catalyse par transfert de phase asymétrique (CATP) solide-liquide. La réaction étudiée est l'addition de Michael asymétrique du malonate de méthyle sur la 2-npentyl cyclopent-2-ène-1-one. En l'absence de solvant classique, mais en présence de 30 équivalents de malonate de méthyle recyclable, d'un catalyseur à base d'alcaloïdes N-alkylés du Cinchina et de carbonate de potassium, nous sommes parvenus à synthétiser chacun des énantiomères désirés avec respectivement 90 et 80% d'excès énantiomérique. Une réaction de déméthoxycarbonylation non racémisante permet d'accéder respectivement aux (+)- et (-)-dihydrojasmonate de méthyle. Nous avons généralisé la méthode à quelques autres substrats accepteurs de Michael avec succès. Nous avons aussi appliqué ce procédé à d'autres nucléophiles potentiels en vue de la synthèse de la cible, mais il semble spécifique du malonate de méthyle.
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Chen, Zhong-Yi, and 陳忠毅. "1. 1. Studies in Synthesis of C-1 Substituted Fulvenes via the Oxidation-Addition of Haloacetyl Halide to fulveneketene Acetal. 2. Traceless Solid-Phase Synthesis of Cyclopenta[c]quinolines and Cyclopenta[c]chromenes via Hetero [6+3] Cycloadditions of Fu." Thesis, 2003. http://ndltd.ncl.edu.tw/handle/12983595954471742161.

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博士
國立中正大學
化學研究所
91
1.Studies in Synthesis of C-1 Substituted Fulvenes via the Oxidation-Addition of Haloacetyl Halide to fulveneketene Acetal. In contrast to the [2+2] cycloaddition of fulvenes and ketenes, fulveneketene acetal, 2-chloropentadienylidene-1,3-dioxalane, reacts with a-halo acyl halides to give various C-1 substituted fulvene. Herein we describe the first example of oxidative-addition of a-chloroacetyl chloride to fulveneketene acetal, and formal synthesis of the carbocyclic analogs of Captopril. 2.Traceless Solid-Phase Synthesis of Cyclopenta[c]quinolines and Cyclopenta[c]chromenes via Hetero [6+3] Cycloadditions of Fulvene. A Facile Approach to the 11-Heterosteroids Framework. The hetero [6+3] cycloaddition of fulvenes to benzoquinones and indoanilines provides an efficient route to the synthesis cyclopenta[c]-4H-chromen-8-ol, benzo[d]cyclopenta[e]-3H-3-azin-8-ol and other 11-hetero steroids. The structure of the cyclopenta[c]chromene skeleton was confirmed by the X-ray structure analysis of the p-bromobenzoate of 109. The traceless solid-phase synthesis of the scaldfold, consist of 110 examples, was achieved by the reaction of benzoquinones or iodoanilines with aminofulvene resin 140 which was prepared from polystyrene amino resin 138 via 2-step reaction.
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Hofmann, Thorsten. "Synthese und Reaktionen von Cyclopenta[c]1,2-diazepinen und Cyclopenta[d]1,2-diazepinen." Phd thesis, 2002. http://tuprints.ulb.tu-darmstadt.de/185/1/dissertation.pdf.

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Bei der Suche nach den Ursachen und der Natur von „Aromatizität“ erwiesen sich zahlreiche nicht-benzoide, carbocyclisch und heterocyclisch konjugierte pi-Elektronensysteme als wertvolle Prüfsteine für quantenchemische Berechnungen. Im Zusammenhang damit war ein Ziel dieser Arbeit, einen Syntheseweg für die bislang unbekannten 4,5-Diazaazulene und 5,6-Diazaazulene zu entwickeln. Durch Reaktionen von semicyclischen 1,5-Diketonen mit verschiedenen Hydrazinen gelang die Darstellung von teilgesättigten literaturunbekannten Cyclopenta[c]1,2-diazepinen, Cyclopenta[d]1,2-diazepinen, Tetraaza[14]annulenen, [1]Pyrindinen und propanoverbrückten alpha-Carbolinen. Verschiedene Methoden zur Dehydrierung der Cyclopenta-1,2-diazepine wurden angewendet, doch führten alle Versuche nicht zu den erwarteten Diazaazulen. Andererseits wäre eine direkte Synthese durch [6+4]-Cycloaddition von 1,2,4,5-Tetrazinen mit Fulvenen denkbar. Doch führten alle Umsetzungen von 2-Cyclopentadienyliden-1,3-dioxolan mit verschieden 1,2,4,5-Tetrazinen unter [4+2]-Cycloaddition zu den entsprechenden Cyclopenta[d]pyridazinen. Neben den schon erwähnten alpha-Carbolinen konnten erstmals auch tricyclische Cyclopenta[d]1,2-diazepine dargestellt werden. Dies ist insbesondere für die Suche nach neuen Leitstrukturen bei der Entwicklung von pharmakologischen Wirkstoffen von Interesse. Alle in der Literatur bisher nicht bekannten Verbindungen wurden mit Hilfe der Massenspektrometrie, Infrarot- und NMR-Spektroskopie sowie Elementaranalysen vollständig charakterisiert. Die Bestimmung der räumlichen Struktur dieser Verbindungen stützt sich dabei im Wesentlichen auf die Ergebnisse zweidimensionaler korrelierter NMR-Experimente und in einigen Fällen auch auf Röntgenstrukturanalysen.
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Book chapters on the topic "Cyclopenta-1"

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Blake, Paul C., Michael F. Lappert, Richard C. Taylor, Paulette N. Hazin, and Joseph W. Bruno. "Bis[η5 -1, 3-Bis(Trimethylsilyl)Cyclopenta-Dienyl]Halouranium(IV) and-Thorium(IV), [MCp″2 Cl2 ] and [UCp″2 X2 ]." In Inorganic Syntheses, 172–77. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132586.ch34.

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Lappert, Michael F., Anirudh Singh, and Josef Takats. "Bis[η5 -1, 3-Bis(Trimethylsilyl)Cyclopenta-Dienyl]Chlorolanthanide(III) Complexes, [{LnCp″2 (μ-Cl)}2 ] and [LnCp″2 Gi-Cl)2 Li(thf)2 ]." In Inorganic Syntheses, 168–72. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132586.ch33.

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Demaison, J. "535 C5H6O 2-Cyclopenten-1-one." In Asymmetric Top Molecules. Part 2, 487–88. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-10400-8_283.

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Winkelmann, J. "Diffusion of cyclopentane (1); air (2)." In Gases in Gases, Liquids and their Mixtures, 1039. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_737.

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Winkelmann, J. "Diffusion of hydrogen (1); methyl-cyclopentane (2)." In Gases in Gases, Liquids and their Mixtures, 1337. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_1006.

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Winkelmann, J. "Diffusion of nitrogen (1); methyl-cyclopentane (2)." In Gases in Gases, Liquids and their Mixtures, 1511. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_1139.

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Winkelmann, J. "Diffusion of oxygen (1); methyl-cyclopentane (2)." In Gases in Gases, Liquids and their Mixtures, 1570. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_1189.

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Winkelmann, J. "Diffusion of argon (1); methyl-cyclopentane (2)." In Gases in Gases, Liquids and their Mixtures, 721. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_450.

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Wohlfarth, Ch. "Viscosity of the mixture (1) cyclopentane; (2) cyclohexane." In Supplement to IV/18, 2348. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_1406.

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Wohlfarth, Ch. "Viscosity of the mixture (1) cyclopentane; (2) toluene." In Supplement to IV/18, 2349–50. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_1407.

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Conference papers on the topic "Cyclopenta-1"

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Ocola, Esther, and Jaan Laane. "VAPOR-PHASE INFRARED AND RAMAN SPECTRA AND THEORETICAL INVESTIGATIONS OF π-TYPE INTRAMOLECULAR HYDROGEN BONDING IN 3-CYCLOPENTEN-1-OL AND 3-CYCLOPENTEN-1-AMINE." In 2020 International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2020. http://dx.doi.org/10.15278/isms.2020.wa02.

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Claudio Herrera Braga, Antonio, and Rodrigo Veludo Malgueiro. "Study of 2-methyl-2-cyclopenten-1-one reductive ozonolysis reaction." In XXIII Congresso de Iniciação Científica da Unicamp. Campinas - SP, Brazil: Galoá, 2015. http://dx.doi.org/10.19146/pibic-2015-37802.

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Reports on the topic "Cyclopenta-1"

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Forster, Nelson H. Carbon-Phenolic Cages for High-Speed Bearings. Part 1 - Friction and Wear Response of Phenolic Composite Impregnated with a Multiply-Alkylated Cyclopentane (MAC) Lubricant and MoS2 Solid Lubricant. Fort Belvoir, VA: Defense Technical Information Center, January 2003. http://dx.doi.org/10.21236/ada416130.

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You might also be interested in the extended bibliographies on the topic 'Cyclopenta-1' for particular source types:
Journal articles
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