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Relevant bibliographies by topics / Bicyclo[2.2.1]heptane

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Academic literature on the topic 'Bicyclo[2.2.1]heptane'

Author: Grafiati

Published: 4 June 2021

Last updated: 10 February 2022

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Journal articles on the topic "Bicyclo[2.2.1]heptane"

1

Werstiuk, N. H., S. Yeroushalmi, and Hong Guan-Lin. "Synthesis of bicyclic diones and thiones. Facile methylation of the enolates of bicyclo[2.2.1]heptane-2,5-dione and bicyclo[2.2.2]octane-2,5-dione. An AM1 computational study of bicyclic enolates." Canadian Journal of Chemistry 70, no. 3 (March 1, 1992): 974–80. http://dx.doi.org/10.1139/v92-130.

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A group of bicyclic ketones and thiones have been synthesized for homenolization studies. Bicyclo[2.2.1]heptane-2,5-dione (6) undergoes unusually rapid tetramethylation giving 3,3,6,6-tetramethylbicyclo[2.2.1]heptane-2,5-dione (1) in good yield. Treatment of 1 with P2S5 in xylene gave 3,3,6,6-tetramethylbicyclo[2.2.1]heptane-2,5-dithione (2) and 3,3,6,6-tetramethyl 15-oxo-bicyclo[2.2.1]heptane-2-thione (3), which was converted into 4 with Raney nickel. Bicyclo[2,2,2]octane-2,5-dione (7), prepared via a Diels–Alder reaction between 2-trimethylsilyloxy-1,3-cyclohexadiene and and α-acetoxyacrylonitrile followed by a one-step desilylation/hydrolysis, also undergoes facile tetramethylation giving 3,3,6,6-tetramethylbicyclo[2.2.2]octane-2,5-dione (5) in good yield. AM1 calculations were carried out on the α-enolates of bicyclo[2.2.1]heptan-2-one, 6, 5-methylidenebicyclo[2.2.1]heptan-2-one, and 4-acetylbicyclo[2.2.1]-heptan-2-one in an attempt to gain information on the source of the enhanced acidity of the C-3 hydrogens of 6 and 7. Keywords: bicyclic ketones, thiones, synthesis.

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Hřebabecký, Hubert, Milena Masojídková, Martin Dračínský, and Antonín Holý. "Synthesis of Novel Conformationally Locked Carbocyclic Nucleosides Derived from 3-(Hydroxymethyl)bicyclo[2.2.1]heptane-2,5-diol." Collection of Czechoslovak Chemical Communications 71, no. 6 (2006): 871–88. http://dx.doi.org/10.1135/cccc20060871.

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(1R*,2R*,3R*,4R*,5R*,6S*)-3-Amino-5-(benzyloxy)-6-(hydroxymethyl)bicyclo[2.2.1]heptan-2-ol (18) was prepared in seven easy steps from benzyl (1R*,2S*,3S*,4S*)-3-(benzyloxy)bicyclo[2.2.1]hept-5-ene-2-carboxylate (10). Reaction of amine18with ethylN-((2E)-3-ethoxymethacryloyl)carbamate afforded 1-[(1R*,2R*,3R*,4R*,5S*,6R*)-6-(benzyloxy)-3-hydroxy-5- (hydroxymethyl)bicyclo[2.2.1]heptan-2-yl]-5-methylpyrimidine-2,4(1H,3H)-dione (21) and after deprotection by transfer hydrogenation, free thymine analogue22. The thymine derivative21was converted to 2,3'-anhydronucleoside26. Treatment of the benzyl derivative18with sodium in liquid ammonia led to amine19, which was used as key intermediate for the construction of (1R*,2R*,3R*,4R*,5R*,6S*)-3-(6-chloro-9H-purin-9-yl)-6-(hydroxymethyl)-bicyclo[2.2.1]heptane-2,5-diol (28) and (1R*,2R*,3R*,4R*,5R*,6S*)-3-(2-amino-6-chloro-9H-purin-9-yl)-6-(hydroxymethyl)bicyclo[2.2.1]heptane-2,5-diol (33). Ammonolysis of28led to 6-amino-9H-purine derivative29. 6-(Dimethylamino)-9H-purine analogue30and 6-(cyclopropylamino)-9H-purine analogues31and34were prepared by aminolysis of corresponding chloropurine derivatives.

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3

Tanase, Constantin I., Anamaria Hanganu, and Constantin Draghici. "Trifluoroacetylation of Alcohols During NMR Study of Compounds with Bicyclo[2.2.1]heptane, Oxabicyclo[3.3.0]octane and Bicyclo[3.3.0]octane Skeleton." Revista de Chimie 72, no. 2 (May 7, 2021): 156–77. http://dx.doi.org/10.37358/rc.21.2.8428.

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TFA was added to a solution of a bicyclo[2.2.1]heptane azide-alcohol in CDCl3 to correctly characterize the compound, but during 24 h gave the trifluoro acetylated compound in quantitative yield. NMR spectra of the esterified compound helped us also to correctly attribute the NMR signals to the protons, and also confirmed the identification of the carbon atoms. The study was extended to other 14 compounds containing a primary alcohol group alone or with an ethylene ketal, a δ- or -lactone group, a primary and a secondary group, two primary and an alkene group and two primary and a secondary alcohol groups on scaffolds containing bicyclo[2.2.1]heptane, oxabicyclo[3.3.0]octane, bicyclo [2.2.1]heptane constrained with a cyclopropane ring and bicyclo[3.3.0]octane fragments. The esterification of all compounds was also quantitative in 24 to 72 h; this helped us to correct attribute the NMR signals to the protons and carbon atoms of the un-esterified compounds by comparison with those of the trifluoro acetylated compounds. A graphical presentation of 1H- and 13C-NMR spectra of a few un-esterified and esterified compounds are presented in the paper.

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4

Liu, Qi Mei, and Wan Xi Peng. "80°С-Based TD-GC/MS Analysis of Chemical Components from Branches of Cinnamomum camphora." Key Engineering Materials 480-481 (June 2011): 466–71. http://dx.doi.org/10.4028/www.scientific.net/kem.480-481.466.

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The analytical result by 80°С-based TD-GC/MS showed that 65 peaks were obtained from the helium volatiles from the fresh branches of Cinnamomum camphora and 60 chemical compounds were identified. The results showed that the main components were as: 1,3-Benzodioxole, 5-(2-propenyl)- (12.629%), Tricyclo[2.2.1.0(2,6)]heptane, 1,7-dimethyl-7-(4-methyl-3-pentenyl)-, (-)- (10.302%), 3-Cyclohexene-1-methanol, .alpha.,.alpha.4-trimethyl- (9.084%), Bicyclo[2.2.1] heptan-2-one, 1,7,7-trimethyl-, (1R)- (7.406%), Nerolidol (6.695%), Bicyclo[2.2.1]heptane, 2-methyl-3-methylene-2-(4-methyl-3-pentenyl)-, (1S-exo)- (6.017%), Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (.+/-.)- (4.885%), Bicyclo[3.1.1]hept-2-ene, 2,6-dimethyl-6-(4-methyl-3-pentenyl)- (4.680%), Naphthalene, 1,2,3,5,6,8a-hexahydro-4,7-dimethyl-1-(1-methylethyl)-, (1S-cis)- (4.139%), 3-Cyclohexen-1-ol, 4-methyl-1-(1-methylethyl)-, (R)- (3.538%), Copaene (2.749%), Bicyclo[2.2.1] heptan-2-ol, 1,7,7-trimethyl-, (1S-endo)- (2.643%), Acetic acid, 1,7,7-trimethyl-bicyclo [2.2.1]hept-2-yl ester (2.536%), Cyclohexane, bromo- (2.530%), 1,6,10-Dodecatriene, 7,11- dimethyl-3-methylene-, (E)- (1.725%), Naphthalene, 1,2,3,4,4a,5,6,8a-octahydro-7-methyl-4- methylene-1-(1-methylethyl)-, (1.alpha.,4a.beta.,8a.alpha.)- (1.265%), Bicyclo[4.4.0]dec-1-ene, 2-isopropyl-5-methyl-9-methylene- (1.174%), (-)-Isosativene (1.149%), 11-Tetradecen-1-ol acetate (1.118%), .alpha.-Cadinol (1.061%), etc. The analytical result suggested that the helium volatiles from the fresh branches of C. camphora could be used as industrial materials of biomedicines, spicery and food industry.

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Wermuth, Urs D., Ian D. Jenkins, Raymond C. Bott, Karl A. Byriel, and Graham Smith. "Some Stereochemical Aspects of the Strecker Synthesis and the Bucherer - Bergs Reaction." Australian Journal of Chemistry 57, no. 5 (2004): 461. http://dx.doi.org/10.1071/ch03202.

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Both the Strecker and Bucherer–Bergs reactions convert the norbornane keto ester methyl bicyclo[2.2.1]hept-6-one-2-endo-carboxylate into the lactam 6-endo-aminobicyclo[2.2.1]heptane-2-endo-carboxylic acid-γ-lactam-6-exo-carboxylic acid. This lactam is unusually stable and cannot be hydrolyzed to the corresponding amino acid. The stereochemistry in the Strecker reaction, in which the amino group is endo, is contrary to that expected from literature precedent. The stereochemistry in the Bucherer–Bergs reaction, in which the amino group is also endo, has been confirmed by X-ray crystallographic analysis of the intermediate spirohydantoin (±)-bicyclo[2.2.1]heptane-2-endo-carboxylic acid-6-spiro-5′-hydantoin.

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Che, Jin-Xin, Zhi-Long Wang, Xiao-Wu Dong, You-Hong Hu, Xin Xie, and Yong-Zhou Hu. "Bicyclo[2.2.1]heptane containing N,N′-diarylsquaramide CXCR2 selective antagonists as anti-cancer metastasis agents." RSC Advances 8, no. 20 (2018): 11061–69. http://dx.doi.org/10.1039/c8ra01806e.

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7

Rehse, Klaus, Peter Sparfeldt, and Wolfgang Kehr. "Neuropsychotrope aktivität dopaminanaloger bicyclo[2.2.1]-heptane." Archiv der Pharmazie 320, no. 10 (October 1987): 1042–50. http://dx.doi.org/10.1002/ardp.198700007.

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8

Liu, Qi Mei, Dang Quan Zhang, Kuan Peng, and Wan Xi Peng. "Deep Analysis on Bioindustry Prospects of 40°С Volatiles of Cinnamomum camphora Branches." Key Engineering Materials 480-481 (June 2011): 266–71. http://dx.doi.org/10.4028/www.scientific.net/kem.480-481.266.

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Cinnamomum camphora has been used to heal some specific diseases in the Chinese Folk for a long time. In order to explore the wide utilization in biomedicine and spicery, the chemical components of helium volatiles from the fresh branches of C. camphora were studied by TD-GC/MS. The analytical result by TD-GC/MS showed that 50 peaks were obtained from the helium volatiles from the fresh branches of C. camphora and 46 chemical compounds representing 99.993% of the total areas were identified. The results showed that the main components were as: Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1R)- (9.620%), 3-Cyclohexene-1- methanol, .alpha.,.alpha.4-trimethyl- (9.425%), 1,3-Benzodioxole, 5-(2-propenyl)- (8.223%), Bicyclo[2.2.1]heptane, 2-methyl-3-methylene-2-(4-methyl-3-pentenyl)-, (1S-exo)- (7.541%), Tricyclo[2.2.1.0(2,6)]heptane, 1,7-dimethyl-7-(4-methyl-3-pentenyl)-, (-)- (6.884%), Bicyclo[3.1.1] hept-2-ene, 2,6-dimethyl-6-(4-methyl-3-pentenyl)- (6.050%), Bicyclo[2.2.1]heptan-2-one, 1,7,7- trimethyl-, (1S)- (4.678%), 1,3-Benzodioxole, 5-(2-propenyl)- (4.500%), Naphthalene, 1,2,3,5,6,8a- hexahydro-4,7-dimethyl-1-(1-methylethyl)-, (1S-cis)- (4.491%), 3-Cyclohexen-1-ol, 4-methyl-1- (1-methylethyl)-, (R)- (4.254%), Copaene (4.120%), Tricyclo[2.2.1.0(2,6)]heptane, 1,7-dimethyl-7- (4-methyl-3-pentenyl)-, (-)- (4.097%), Acetic acid, 1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester (3.574%), Borneol 3.334%), 3-(4-N,N-Dimethylaminophenyl)propenoic acid, 2- (diethoxyphosphinyl)-, ethyl ester (2.809%), Eucalyptol (2.096%), 1,6,10-Dodecatriene, 7,11- dimethyl-3-methylene-, (Z)- (1.885%), (-)-Isosativene (1.664%), 1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl- (1.407%), Cyclohexene, 1-methyl-4-(5-methyl-1-methylene-4-hexenyl)-, (S)- (1.218%), 1,4-Methanoazulene, decahydro-4,8,8-trimethyl-9-methylene-, [1S-(1.alpha.,3a.beta., 4.alpha.,8a.beta.)]- (1.174%), .alpha.-Caryophyllene (1.156%), etc. The analytical result suggested that the helium volatiles from the fresh branches of C. camphora can be applicable to biomedicine and spicery industrial materials.

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Tanase, Constantin I., Constantin Draghici, Catalina Negut, and Lucia Pintilie. "New Constrained Amines in a Bicyclo[2.2.1]Heptane Skeleton." Revista de Chimie 69, no. 9 (October 15, 2018): 2448–53. http://dx.doi.org/10.37358/rc.18.9.6551.

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In this paper we present an efficient procedure for obtaining ether-protected bicyclo[2.2.1]heptane amines in six steps, from an optically active keto-alcohol norbornane compound, for building the heterocyclic bases of pyrimidine and purine constrained nucleosides. Trityl as protecting group makes it possible to isolate 5-endo-compounds in pure form by selective crystallization, and to isolate the intermediates in the next 3 steps of the reaction by crystallization. With TBDMS, all compounds were obtained as oil. The direct selective reduction of the keto-alcohol norbornane compound gave the pure 5-endo-diol 4d in high yield, which was then selectively protected at the primary hydroxyl with a trityl group; the next steps are similar for obtaining the trityl-protected bicyclo[2.2.1]heptane amine. The azide intermediates are valuable intermediates for click chemistry.

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10

Šála, Michal, Hubert Hřebabecký, Martin Dračínský, Milena Masojídková, Armando M. De Palma, Johan Neyts, and Antonín Holý. "Synthesis of novel racemic carbocyclic nucleosides derived from 5,6-disubstituted norbornene." Collection of Czechoslovak Chemical Communications 75, no. 1 (November 28, 2009): 1–20. http://dx.doi.org/10.1135/cccc2009116.

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Novel class of the carbocyclic nucleosides based on bicyclo[2.2.1]heptene/heptane was prepared by two approaches. Thymine analogues were synthesized starting from methyl (1R*,4S*)-bicyclo[2.2.1]hepta-2,5-diene-2-carboxylate1by Michael addition of the thymine salt to the double bond as the key step. The yield and ratio of the isomers of this reaction depended on the used base (DBU, K2CO3). Purine nucleoside analogues were synthesized by the linear synthesis, the purine nucleobase was build-up on the amino group. The amino groups (exo/endoconfiguration) were introduced to the scaffold by the Curtius rearrangement. Norbornene analogues were converted to saturated andcis-hydroxylated nucleoside derivatives. [(1R*,2S*,3S*,4S*)-3-(6-Chloro-9H-purin-9-yl)bicyclo[2.2.1]hept-5-en-2-yl]methanol (13a) and [(1R*,2R*,3R*,4S*)-3-(6-chloro-9H-purin-9-yl)bicyclo[2.2.1]hept-5-en-2-yl]methanol (13b) showed moderate activity againstCoxsackievirus CVB3.

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Dissertations / Theses on the topic "Bicyclo[2.2.1]heptane"

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Jung, Céline. "Etude des équilibrations et de la solvatation d'alcools épimères dans la série du bicyclo[2.2.1]heptane." Doctoral thesis, Universite Libre de Bruxelles, 1986. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/213553.

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Karimiahmadabadi, Mansoureh. "Novel Pentofuranose Chemistry to Modulate RNA Function." Doctoral thesis, Uppsala universitet, Kemisk biologi, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-233898.

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Chemical modifications of oligonucleotides provide an important tool to understand how the natural substrate works as well as how to improve their biochemical and biological properties as potential therapeutics and diagnostics. Our carba-LNA (2',4'-carba-bridged Locked Nucleic Acid) modified oligo-DNA or -RNA have been found to be useful to modulate oligo-RNA and -DNA activity. This thesis is based on four papers: Paper I (J. Org. Chem. 2010, 75, 7112-7128) deals with the synthesis of 2',4'-propylene-bridged (Carba-ENA) thymidine and its analogues. These carba-ENA nucleosides have been subsequently incorporated into 15mer antisense oligodeoxynucleotides (AON), and their affinity toward complementary mRNA and DNA, as well as their nuclease resistance and RNase H recruitment capability have been investigated in comparison with those of the native and ENA counterparts. Paper II (J. Org. Chem. 2012, 77, 6855–6872) illustrates the synthesis of dimethylbicyclo[2.2.1]heptane and a diastereomeric mixture of oxabicyclo[2.2.1]heptanes by the free-radical ring-closure reaction approach. The role of steric factors for different chair- and the boat-like transition states was evaluated involving the 5-exo radical ring closure reaction to a tethered olefin. Paper III (J. Org. Chem. 2012, 77, 9747-9755) shows an unusual strain releasing reaction of 1-mesyloxy-8,7-dimethylbicyclo[2.2.1]heptane by a base-promoted substitution at the chiral C3 followed by spontaneous concerted ring opening involving the most strained C2-C3-C4 bonds (with bond angle 94°) and the C2 bridgehead leading to anti-endo elimination of the C1-mesyloxy group by the conjugate base of adenine or thymine to give two diastereomeric C3'(S) and C3'(R) derivatives of 1-thyminyl and 9-adeninyl cyclohexene, and a mechanistic rational has been formulated. Paper IV (J. Org. Chem. 2014, 79, 7266−7276) focuses on the diastereospecific synthesis of E/Z bicyclo[2.2.1]heptane-7- and oxabicyclo[2.2.1]heptane-8-oximes and their corresponding C-nitroso derivatives. The comparative kinetic and thermodynamic studies of the conversions of the C-nitroso side products to the required oximes have been delineated leading to the synthesis of desmethyl sugar derivatives.

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Dorok, Sascha. "Erzeugung und Folgechemie von Bicyclo[2.1.1]hex-1-ylhalogen- und Bicyclo[2.2.1]hept-1-ylhalogencarbenen." Doctoral thesis, [S.l. : s.n.], 2003. http://deposit.ddb.de/cgi-bin/dokserv?idn=970415109.

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Hachisu, Shuji. "Radical rearrangement of bicyclo [2.2.1] systems and application in kainoid synthesis." Thesis, University of Oxford, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.414142.

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Al-Rubaye, Huda Ismail. "Synthesis of analogues of epibatidine based on the 2-azabicyclo[2.2.1]heptane system." Thesis, University of Leicester, 2018. http://hdl.handle.net/2381/42393.

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Epibatidine (exo-2-(6-chloro-3-pyridyl)-7-azabicyclo[2.2.1]heptane) is an alkaloid isolated from the skin of the Ecuadorian poison frog. It has been known since 1992 and has high binding affinity for nicotinic acetylcholine receptors. Many studies have reported epibatidine to possess analgesic properties, but it is also toxic even in low doses, thus, it cannot be used therapeutically. A wide range of epibatidine analogues have been studied in the hope of reducing their toxicity, and hence exploiting their therapeutic potential A general method for the synthesis of anti-7-functionalised 2-benzyl-2-azabicyclo[2.2.1]heptane has been employed. Aza Diels-Alder reaction was used successfully to construct the rigid protected amine 2-benzyl-2-azabicyclo[2.2.1]hept-5-ene skeleton. Bromination of 2-benzyl-2-azabicyclo[2.2.1]hept-5-ene gives a reactive tricyclic salt, which in turn undergoes skeletal rearrangement with hydrid to obtain anti-7-bromo-2-benzyl-2-azabicyclo[2.2.1]heptane. Nucleophilic substitution reaction at C-7 of this compound found to be occur with retention of configuration, consistent with neighbouring group participation of the bicyclic nitrogen lone pair. An oxidation-reduction strategy facilitated the epimerisation at the C-7 of 2-azabicyclo[2.2.1]heptane, heterocycles have been introduced at this position to give the ether linkage nicotinic receptor ligands with general structure 7-(pyridyloxy)-2-benzyl-2-azabicyclo[2.2.1]heptane. Mitsunobu chemistry has been utilised to synthesis a range of pyridyl ether compounds. Methylisoxazole heterocycle has also been synthesised and incorporated to open the way to some analogues. The synthesis of fluorinated analogues of 2-azabicyclo[2.2.1]heptane has been investigated using nucleophilic fluorinating agent, diethylaminosulphur trifluoride, DAST. Moreover, fluorination of all alcohols is consistent with SN2 attack, whilst fluorination of ketones gave geminal difluorides with the 6-oxo isomer being assisted by neighbouring group participation. A range of different 5- and 6-chloropyridyl-substituted-2-azabicyclo[2.2.1]heptane derivatives have been constructed. The 5- and 6-chloropyridyl derivatives were synthesised via nucleophilic attack of lithiated-chloropyridine onto the appropriate azabicyclic ketone. Dehydration of the adduct gave an olefin. 1H, 13C and 19F NMR spectroscopy was used to characterise these compounds.

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Chen, Yao-Jung. "Secondary amine catalyzed-oximation of cyclopentanone and basicity and reactivity of 1-azabicyclo[2.2.1]heptane /." The Ohio State University, 1986. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487265555441794.

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Terranova, Eric. "Poplynorbonène : étude de l'oxydation d'un modèle et de dérivés bicyclo [2.2.1] héptaniques catalysée par le ruthénium." Aix-Marseille 3, 1989. http://www.theses.fr/1989AIX30089.

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8

Bonfantini, Edia. "Synthèse et réactivité des complexes carbonylfer du (dimethoxymethyl)-1 dimethylidène-5,6 oxa-7 bicyclo(2.2.1)heptène-2 /." [S.l.] : [s.n.], 1990. http://library.epfl.ch/theses/?nr=827.

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Taylor, David. "Reactions of 2-azabicyclo[2.2.1] heptane systems and their application in the synthesis of peptide and amino acid analogues." Thesis, Heriot-Watt University, 2001. http://hdl.handle.net/10399/480.

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10

Aziz, Mostafa. "Synthèse de produits naturels et des racémiques correspondants comportant le squelette du triméthyl-1,3,3 oxa-7 bibyclo(2.2.1.)heptane." Grenoble 2 : ANRT, 1987. http://catalogue.bnf.fr/ark:/12148/cb376024944.

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Books on the topic "Bicyclo[2.2.1]heptane"

1

Tam, William W. L. Transition metal catalyzed [2[pi]+2[pi]+2[pi]] and [2[pi]+2[pi]+4[pi]] cycloadditions of bicyclo[2.2.1]hepta-2,5-dienes: Scope & applications. 1996.

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Book chapters on the topic "Bicyclo[2.2.1]heptane"

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Whitesell, James K., and Mark A. Minton. "Bicyclo[2.2.1]heptanes." In Stereochemical Analysis of Alicyclic Compounds by C-13 NMR Spectroscopy, 55–92. Dordrecht: Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3161-9_6.

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2

Vogt, J. "661 C7H8 Bicyclo[2.2.1]hepta-2,5-diene." In Asymmetric Top Molecules. Part 3, 154. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-14145-4_83.

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3

Winkelmann, Jochen. "Diffusion coefficient of 1,7,7-trimethyl-bicyclo[2.2.1]heptane-2,3-dione in 2-hydroxy-benzoic acid phenyl ester." In Diffusion in Gases, Liquids and Electrolytes, 1339. Berlin, Heidelberg: Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54089-3_903.

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4

Penczek, Stanislaw, Ryszard Szymanski, Julia Pretula, Krzysztof Kaluzynski, and Jan Libiszowski. "Copolymerization of 7-Oxabicyclo[2.2.1]heptane with Tetrahydrofuran." In ACS Symposium Series, 75–82. Washington, DC: American Chemical Society, 1997. http://dx.doi.org/10.1021/bk-1997-0665.ch007.

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5

Moreno-Vargas, Antonio J., and Pierre Vogel. "Synthesis of 7-Oxabicyclo[2.2.1]heptane and Derivatives." In Synthesis of Saturated Oxygenated Heterocycles I, 141–88. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-41473-2_4.

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Vogt, J. "622 C6H11ClO 7-Oxabicyclo[2.2.1]heptane - hydrogen chloride (1/1)." In Asymmetric Top Molecules. Part 3, 92–93. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-14145-4_44.

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Vogt, J. "623 C6H11FO 7-Oxabicyclo[2.2.1]heptane - hydrogen fluoride (1/1)." In Asymmetric Top Molecules. Part 3, 94–95. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-14145-4_45.

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Winkelmann, J. "Diffusion of 6,6-dimethyl-2-methylene-bicyclo[3.1.1]heptane (1); carbon dioxide (2)." In Gases in Gases, Liquids and their Mixtures, 1729. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_1308.

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Cibulka, I., J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Heat of Mixing and Solution of Heptane C7H16 + C10H18 cis-Bicyclo[4.4.0]decane (HMSD1111, LB4080_H)." In Binary Liquid Systems of Nonelectrolytes II, 368–69. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-23277-0_153.

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Kan, Wai Ming, and Yung Lee Yek. "Synthesis of Novel 7-Oxabicyclo[2.2.1]-Heptane Thromboxane A2 Derivatives Containing Substitution on Positions One and Two." In Advances in Experimental Medicine and Biology, 497–501. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-1-4899-1813-0_74.

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Conference papers on the topic "Bicyclo[2.2.1]heptane"

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Tanase, Constantin, Constantin Draghici, and Miron Theodor Caproiu. "Key Intermediates for introducing a bulky bicyclo[3.3.0]heptane skeleton in the w-side chain to reduce the enzyme inactivation of prostaglandins." In The 24th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2020. http://dx.doi.org/10.3390/ecsoc-24-08390.

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