Relevant bibliographies by topics / Bicyclo[3

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

Academic literature on the topic 'Bicyclo[3'

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

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Journal articles on the topic "Bicyclo[3"

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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 (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-acetoxyacrylon
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Chen, Shi Peng, Jian Ting Zhang, Dong Wang Liu, et al. "A Prophase Study on Applying Conia-Ene Reation in Constructing bicyclo [3, 3, 1] Nonane Ring." Advanced Materials Research 781-784 (September 2013): 1172–74. http://dx.doi.org/10.4028/www.scientific.net/amr.781-784.1172.

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The bicyclo [3, 3, 1] nonane ring system is the main structural feature in the lycopodium alkaloids. There are many methods to build the [3, 3, 1] bridged ring system, Herein, we designed to use indium Lewis acid which can activate the triple bond to construct [3, 3, 1] bridged ring system via Conia-ene reaction, and described a prophase study of applying Conia-ene reaction to construct such bicycle [3, 3, 1] nonane ring.
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Binder, Herbert, Walter Matheis, Gernot Heckmann, Hans-Jörg Deiseroth та Han Fu-Son. "Über bicyclische Diacyloxy-pentafluoro-μ3-oxotriborane 2.2.6.10.10-Pentafluoro-4.8-dialkyl-1.3.5.7.9-pentaoxa-2.6.10-triborabicyclo(4.4.0)decadiene: Darstellung, Molekül- und Kristallstruktur". Zeitschrift für Naturforschung B 40, № 7 (1985): 934–41. http://dx.doi.org/10.1515/znb-1985-0715.

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Abstract Bicyclic acyloxyfluoroboranes 3 react with BF3 by an insertion reaction to form bicyclic diacyloxy- pentafluoro-μ3-oxotriboranes of the 2.2.6.10.10-pentafluoro-4.8-dialkyl-1.3.5.7.9-pentaoxa- 2.6.10-tribora-bicyclo(4.4.0)decadiene type 4. A X-ray crystal structure determination of 4b is reported. NM R data of 4b in the solid state and in solution are discussed.
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Hřebabecký, Hubert, Milena Masojídková, and Antonín Holý. "Synthesis of Novel Conformationally Locked Carbocyclic Nucleosides Derived from 5,5- and 6,6-Bis(hydroxymethyl)bicyclo[2.2.1]heptan-2-ol." Collection of Czechoslovak Chemical Communications 70, no. 4 (2005): 519–38. http://dx.doi.org/10.1135/cccc20050519.

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(1R*,2R*,3R*,4S*)-3-Amino-6,6-bis(hydroxymethyl)bicyclo[2.2.1]heptan-2-ol (13) was prepared from (bicyclo[2.2.1]hept-5-ene-2,2-diyl)dimethyl dibenzoate (7) viacis-diol8, cyclic sulfate10, and azide12. (1R*,2R*,3S*,4S*)-3-Amino-6,6-bis(hydroxymethyl)bicyclo[2.2.1]-heptan-2-ol (18) and (1R*,2S*,3S*,4S*)-3-amino-5,5-bis(hydroxymethyl)bicyclo[2.2.1]heptan-2-ol (19) were obtained by addition of chromyl azide to double bond of7, chromatographic separation, debenzoylation and hydrogenation of resulting azides14and16. The amines13,18, and19were used to build (1R*,2R*,3R*,4S*)- (21a), (1R*,2R*,3S*,4S*)
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YAMAMOTO, T., T. EKI, S. NAGUMO, H. SUEMUNE, and K. SAKAI. "ChemInform Abstract: Novel Skeletal Transformation of Bicyclo(3.3.0)octanones to Bicyclo(3. 2.1)octenes." ChemInform 22, no. 50 (2010): no. http://dx.doi.org/10.1002/chin.199150080.

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Zhu, Fang-Hua, Jun-Xiao Yang, Zhi-Hua Mao, and Ru-Gang Xie. "1-[Bicyclo[4.2.0]octa-1(6),2,4-trien-3-yl]-3-[bicyclo[4.2.0]octa-1(6),2,4-trien-3-ylmethyl]imidazolium hexafluorophosphate." Acta Crystallographica Section E Structure Reports Online 64, no. 2 (2008): o434. http://dx.doi.org/10.1107/s1600536807067086.

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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 d
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Liu, Qi Mei, та Wan Xi Peng. "80°С-Based TD-GC/MS Analysis of Chemical Components from Branches of Cinnamomum camphora". Key Engineering Materials 480-481 (червень 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
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Loughlin, Wendy A. "A Facile Approach to Bicyclo[n.2.0]alkan-1-ols: An Overview." Australian Journal of Chemistry 57, no. 4 (2004): 335. http://dx.doi.org/10.1071/ch03213.

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Bicyclo[n.2.0]alkan-1-ols are an integral part of various frameworks of natural products. The reaction of the lithium enolates of simple ketones with (±)-phenyl vinyl sulfoxide and the controlled formation of bicyclo[n.2.0]alkan-1-ols was investigated. Facile access to bicyclo[n.2.0]alkan-1-ols (n = 3–6) bearing a bridgehead hydroxyl group was obtained. The ratio of bicyclo[n.2.0]alkan-1-ols (n = 3–6) to alkyated ketone was found to be dependent on enolate reactivity, electrophile conversion, time, reaction temperature, concentration, as well as the stability and steric strain observed in the
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Ahlenstiel, Eckart, Wolfgang Kliegel, Steven J. Rettig, and James Trotter. "Structural studies of organoboron compounds. LVII. Synthesis and structure of bicyclic boron-nitrogen betaines. 1-Methyl-5-(3-nitrophenyl)-4,6,9-trioxa-1-azonia-5-boratabicyclo[3.3.1]nonane and 3,3,4-trimethyl-1-(3-nitrophenyl)-2,6,7-trioxa-3-azonia-1-boratabicyclo[2.2.2]octane." Canadian Journal of Chemistry 71, no. 2 (1993): 263–71. http://dx.doi.org/10.1139/v93-038.

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The syntheses and structures of the bicyclic boron-nitrogen betaines 1-methyl-5-(3-nitrophenyl)-4,6,9-trioxa-1-azonia-5-boratabicyclo[3.3.1]nonane, 7a, and 3,3,4-trimethyl-1-(3-nitrophenyl)-2,6,7-trioxa-3-azonia-1-boratabicyclo[2.2.2]-octane, 14a, are reported. Crystals of 7a are orthorhombic, a = 20.256(2), b = 37.652(2), c = 6.642(1) Å, Z = 16, space group Fdd2, and those of 14a are orthorhombic, a = 21.402(2), b = 11.334(3), c = 11.248(2) Å, Z = 8, space group Pbca. The structures were solved by direct methods and were refined by full-matrix least-squares procedures to R = 0.038 and 0.045 (
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Dissertations / Theses on the topic "Bicyclo[3"

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Gregg, Timothy Morgan. "Diastereoselective manipulations and conformational calculations of enantiomerically pure bicyclo(M.1.0)alkan-2-ones and bicyclo(M.1.0)alk-3-en-2-ones." Diss., The University of Arizona, 1995. http://hdl.handle.net/10150/187294.

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Medium- and large-sized cycloalkanones with adjacent fused cyclopropyl rings are excellent substrates for highly diastereoselective reactions. We attribute the high selectivity of these reactions to local conformational rigidity around the stereo genic cyclopropane ring in these otherwise flexible systems. Addition of a variety of nucleophiles to these compounds, where the large ring ranged from eight- to 16-membered, gave cyclopropyl carbinols with >20:1 stereoselectivity. Crystallographic analysis of the products in several cases confirmed that the favored approach of the nucleophile is anti
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Stahl, Matthew Timothy. "Conformational analysis and nucleophilic addition transition state modeling of bicyclo(m.1.0)alkan-2-ones and bicyclo(m.1.0)alk-3-en-2-ones." Diss., The University of Arizona, 1995. http://hdl.handle.net/10150/187429.

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Medium and large ring bicyclo (m.1.0) alkan-2-ones and bicyclo (m.1.0) alk-3-en-2-ones are ideal starting materials for stereoselective organic synthesis. Readily available in many ring sizes and in enantiomerically pure form, such carbocyclic skeleta provide entry into numerous natural products. Reactions such as 1,2-addition, α-alkylation, and 1,4-addition have been shown to proceed with high diastereoselectivity due to local conformational anchoring of the cyclopropyl ketone function. In an effort to elucidate the mechanisms of diastereoselectivity and to augment the synthetic utility, comp
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GUO, YUPING. "Synthese du 11,11-dimethyl bicyclo 5. 3. 1 undec-3,8-diene, sous-structure a/b du taxol." Paris 11, 1992. http://www.theses.fr/1992PA112206.

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Ce travail se divise en deux parties et a pour but l'elaboration des cycles a et b du taxol 5, une substance naturelle aux proprietes antitumorales. Nos efforts ont ete concentres sur l'etude des fragmentations regioselectives de la liaison c4-c12 de 4,8,11-trimethyl-5-methoxy-12-oxo-2,5-epoxytricyclo 5. 31#4#,#1#1 dodecene-8 39, ouvrant une nouvelle voie d'acces aux derives du taxol. La premiere partie decrit les differentes tentatives d'agrandissement de cycle par fragmentations heterolytiques, via la reaction de haller-bauer, le systeme base-solvant: ko-t-bu/h#2o-dmso et la reaction de grob
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Jacquet, Fabienne. "Obtention de l'hydroxy-4 dioxa-2,6 bicyclo (3. 3. 0) octanone-8 (1S, 4S, 5R) par voie catalytique, et selon un procédé d'électrosynthèse organique." Toulouse, INPT, 1986. http://www.theses.fr/1986INPT023G.

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Zeghdoudi, Rachida. "Contribution à la synthèse totale des dérivés du taxane." Paris 11, 1988. http://www.theses.fr/1988PA112083.

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Cette thèse constitue une contribution à la synthèse de dérivés du taxane, groupe de diterpènes dont certains manifestent une activité antileucémique et antitumorale prononcée. Le squelette de ces composés (appelé taxane) comprend trois cycles : A, B et C dont le cycle B à huit chaînons. La stratégie adoptée consiste à construire successivement :A→AB→ ABC. La première partie de ce travail décrit la synthèse de dérivés diméthyl-9,9 bicycle [3. 3. 1] nonadione-2,4, renfermant le cycle A. La deuxième partie concerne la préparation, en deux étapes (réaction de de 1AYO, suivie d'une rétroaldolisati
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Carret, Sébastien. "Approche générale, efficace et sélective de produits naturels possédant le squelette Bicyclo [5. 3. 0] décane : synthèse d'Azulènes et de Guaianolides." Université Joseph Fourier (Grenoble), 2005. http://www.theses.fr/2005GRE10230.

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La cycloaddition [2+2] du dichlorocétène, sur des cycloheptatriènes mono substitués conduit après expansion de cycle au diazométhane et déshydrohalogénation, de façon régio- et stéréosélective, à des alpha-chlorotriénones. Ces intermédiaires se sont déjà avérés des synthons particulièrement attractifs pour la synthèse totale de produits naturels possédant le squelette bicyclo[5. 3. 0]décane. L'utilisation d'organozinciques, de cétènes-acétals et des conditions de couplage de Suzuki, nous a permis d'élaborer une approche générale et régiosélective des azulènes polysubsitués parmi lesquels de no
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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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Heinrich, Clément. "Des alcynyl-cétones fonctionnalisées : vers la synthèse de squelettes carbonés originaux." Thesis, Strasbourg, 2016. http://www.theses.fr/2016STRAF001/document.

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Les travaux décrits dans ce mémoire de thèse ont pour objet d'une part l'étude de la réactivité de céto-3-alcynoates et de céto-sulfonylynamides. Les céto-3-alcynoates conduisent à la formation d'allénoates bi- ou tricycliques par catalyse au carbonate de césium. La sélectivité est totale au niveau de l'allénoate bicyclique obtenu. Il est également possible d'effectuer cette réaction de cyclisation de façon monotope au départ de l'alcynyl-cétone correspondante, dans ce cas les allénoates tricycliques sont obtenus avec de très bons rendements. Les 3-alcynoates peuvent également être utilisés po
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Calancea, Mihaela. "Approche Générale et Efficace des Terpénoïdes Possédant le Squelette Bicyclo[5. 3. 0]décane : Synthèse de Sesquiterpènes (Aromadendranes, Guaianes et Tri-nor-guaianes) et Approche des Diterpènes." Université Joseph Fourier (Grenoble), 2008. http://www.theses.fr/2008GRE10105.

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La cycloaddition [2+2] du dichlorocétène sur des cycloheptatriènes monosubstitués conduit, après expansion de cycle au diazométhane et déshydrohalogénation, de façon régio- et stéréosélective, à des alpha-chlorotriénones. Ces intermédiaires se sont déjà avérés des synthons particulièrement attractifs pour la synthèse totale de produits naturels possédant le squelette bicyclo[5. 3. 0]décane. Une cyclopropanation régio- et diastéréosélective avec l'ylure de soufre sur l'alpha-chlorotriénone nous a permis d'élaborer une approche générale des aromadendranes ainsi que la synthèse totale de la (±)-c
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Guilini, Pauline. "Synthèse de nouveaux inhibiteurs des fonctions plaquettaires, antagonistes des récepteurs P2Y1 et P2Y12." Strasbourg, 2011. http://www.theses.fr/2011STRA6189.

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Les maladies ischémiques, causées principalement par des thromboses artérielles, sont la première cause de mortalité dans les pays développés. Les antiagrégants plaquettaires sont des médicaments destinés à empêcher la formation des thromboses artérielles. Une stratégie thérapeutique consiste à inhiber les récepteurs responsables de l’activation des plaquettes : le récepteur P2Y12 et le récepteur P2Y1. Pour obtenir une réponse optimale d'agrégation des plaquettes, l'activation synergique des deux récepteurs P2Y1 et P2Y12 a été démontrée. Le travail décrit dans ce mémoire concerne la synthèse d
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Books on the topic "Bicyclo[3"

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Lawrie, Robin. Fear 3.1. Stone Arch Books, 2007.

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Lawrie, Robin. Radar riders. Stone Arch Books, 2007.

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Lawrie, Robin. First among losers. Stone Arch Books, 2007.

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Pato va en bici. Ed. Juventud, 2002.

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Ya zi qi che ji. Xiao lu wen hua shi ye gu fen you xian gong si, 2003.

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Duck on a bike. Blue Sky Press, 2002.

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Shannon, David. Duck on a bike. Blue Sky Press, 2002.

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Shannon, David. Duck on a bike. Blue Sky Press, 2002.

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Crown. Coaster & 3 Speed Bicycle Repa. Crown, 1988.

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Caesar's Bicycle (Timeline Wars/John Barnes, No 3). Eos, 1997.

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Book chapters on the topic "Bicyclo[3"

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

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Cibulka, I., L. Hnědkovský, J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture cis-Bicyclo[4.4.0]decane C10H18 + C10H18 trans-Bicyclo[4.4.0]decane (LB1803, VMSD1112)." In Binary Liquid Systems of Nonelectrolytes. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-73584-7_2770.

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Cibulka, I., L. Hnědkovský, J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture cis-Bicyclo[4.4.0]decane C10H18 + C10H18 trans-Bicyclo[4.4.0]decane (LB1799, VMSD1211)." In Binary Liquid Systems of Nonelectrolytes. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-73584-7_2771.

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Cibulka, I., J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture Cyclopentane C5H10 + C10H18 Bicyclo[4.4.0]decane (VMSD1111, LB3152_V)." In Binary Liquid Systems of Nonelectrolytes I. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-02935-6_272.

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Cibulka, I., J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture Cyclopentane C5H10 + C10H18 Bicyclo[4.4.0]decane (VMSD1212, LB3407_V)." In Binary Liquid Systems of Nonelectrolytes I. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-02935-6_273.

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Cibulka, I., J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture Cyclohexane C6H12 + C10H18 Bicyclo[4.4.0]decane (VMSD1111, LB3153_V)." In Binary Liquid Systems of Nonelectrolytes I. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-02935-6_274.

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Cibulka, I., J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture Cyclohexane C6H12 + C10H18 Bicyclo[4.4.0]decane (VMSD1212, LB3160_V)." In Binary Liquid Systems of Nonelectrolytes I. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-02935-6_275.

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Cibulka, I., J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture Cyclooctane C8H16 + C10H18 Bicyclo[4.4.0]decane (VMSD1111, LB3159_V)." In Binary Liquid Systems of Nonelectrolytes I. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-02935-6_276.

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Cibulka, I., J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture Cyclooctane C8H16 + C10H18 Bicyclo[4.4.0]decane (VMSD1212, LB3163_V)." In Binary Liquid Systems of Nonelectrolytes I. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-02935-6_277.

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Cibulka, I., J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture Bicyclo[4.4.0]decane C10H18 + C10H20 Cyclodecane (VMSD1211, LB4886_V)." In Binary Liquid Systems of Nonelectrolytes I. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-02935-6_279.

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Conference papers on the topic "Bicyclo[3"

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Jonsson, Stefan, and Jon Geirsson. "Synthesis and Ring-Enlargement of Bicyclo[3.3.1]nonan-3-ones." In The 1st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 1997. http://dx.doi.org/10.3390/ecsoc-1-02043.

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Layton, Bradley, Lauren Jablonowski, Ryan Kirby, and Nicholas Lampe. "Bicycle Infrastructure Development Strategy for Suburban Commuting." In ASME 2007 International Mechanical Engineering Congress and Exposition. ASMEDC, 2007. http://dx.doi.org/10.1115/imece2007-42233.

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We present a “Bicycle Highway” transportation alternative to automobile commuting by exploring avenues for reducing perceived impediments to bicycle commuting. The three primary goals of the project are: 1) Address the American diabetes and obesity epidemics by making exercising on a daily basis a more desirable and viable alternative. 2) Address the problem of greenhouse gas emissions and pollutants by partially replacing combustion engines with human-powered transportation. 3) Address the problem of the United States’ dependence on foreign oil by diminishing energy demand for short-range tra
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Doval, Peter N., and Ilya V. Avdeev. "Investigation of Riding Position Effects on Time-Trial Bicycle Drag Coefficient at Different Yaw Angles." In ASME 2012 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/imece2012-88247.

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Time-trial bicycle racing is highly influenced by aerodynamics, perhaps more so than any other form of bicycle racing. Companies competing in this class of racing spend millions of dollars trying to optimize the geometry of the bicycles and the gear each rider wears in order to reduce aerodynamic drag. The idea behind this project was to investigate other ways to optimize the aerodynamic efficiency of the rider, considering that the rider contributes the majority of the drag force of the bicycle-rider system. A large contributor to drag is the frontal area of the object of interest (a silhouet
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Doria, Alberto, and Edoardo Marconi. "A Testing Method for the Prediction of Comfort of City Bicycles." In ASME 2018 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/detc2018-85128.

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An experimental/numerical method for predicting bicycle comfort from laboratory tests is presented. The frequency response functions of the seat post and of the handlebar stem are measured by means of impulsive excitation applied on vibrating tables placed under the front and rear wheel. The interference between front and rear excitation, which occurs on the road, is taken into account by numerically calculating the correlated frequency response function. Numerical calculations based on the concept of vehicle mission make it possible to manage the dependence of acceleration on forward speed an
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Lee, Seung Chul, Sanghun Lee, Ji Hoon Lee, Wonjin Cho, and Ji Yeon Jo. "PA 13-3-0865 The preventive effects of bicycle helmets on clinical outcomes in bicycle-related crashes." In Safety 2018 abstracts. BMJ Publishing Group Ltd, 2018. http://dx.doi.org/10.1136/injuryprevention-2018-safety.80.

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Kondo, Michelle, Christopher Mirroson, Erick Guerra, Elinore Kaufman, and Douglas Wiebe. "3 Where do bike lanes work best? a bayesian spatial model of bicycle lanes and bicycle crashes." In SAVIR 2017. BMJ Publishing Group Ltd, 2017. http://dx.doi.org/10.1136/injuryprev-2017-042560.3.

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Gang Liu, Hongbin Ren, Sizhong Chen, and Wenzhu Wang. "The 3-DoF bicycle model with the simplified piecewise linear tire model." In 2013 International Conference on Mechatronic Sciences, Electric Engineering and Computer (MEC). IEEE, 2013. http://dx.doi.org/10.1109/mec.2013.6885617.

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Dressel, Andrew E., and Adeeb Rahman. "Benchmarking Bicycle and Motorcycle Equations of Motion." In ASME 2011 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. ASMEDC, 2011. http://dx.doi.org/10.1115/detc2011-47344.

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In 2007, Meijaard, et al. [1] presented the canonical linearized equations of motion for the Whipple bicycle model along with test cases for checking alternative formulations of the equations of motion or alternative numerical solutions. This paper describes benchmarking three other implementations of bike equations of motion: the linearized equations for bicycles written by Papadopoulos and Schwab [2] in JBike6, the non-linear equations for bicycles outlined by Schwab [3] and implemented in MATLAB as a Cornell University class project, and the non-linear equations for motorcycles implemented
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Santana, Lourenço Luis Botelho de, and Silvio Cunha. "Aza-bicycles Synthesis Through Formal Aza [3+3], [3+2+1] and [3+1+1+1] Cycloadditions Between Enaminones, Aldehydes and Meldrum’s Acid Derivatives." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0056-1.

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Kishibe, Shun, Yusuke Miyazaki, Osamu Nomura, et al. "PA 04-3-0464 Fall injury in infants while the patient is operating a bicycle." In Safety 2018 abstracts. BMJ Publishing Group Ltd, 2018. http://dx.doi.org/10.1136/injuryprevention-2018-safety.23.

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Reports on the topic "Bicyclo[3"

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Brown, H. C., K. Ganesan, and R. K. Dhar. Enolboration 3. An Examination of the Effect of Variable Steric Requirements of R on the Stereoselective Enolboration of Ketones with R2BCl/Et3N. Bis(Bicyclo(2.2.2)Octyl)Chloroborane/Triethylamine - A New Reagent Which Achieves the Selective Generation of E Enolborinates from Representative Ketones. Defense Technical Information Center, 1992. http://dx.doi.org/10.21236/ada250066.

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