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Relevant bibliographies by topics / Cyclopropane-1,1-dicarboxylate / Journal articles

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Journal articles on the topic 'Cyclopropane-1,1-dicarboxylate'

Author: Grafiati

Published: 4 June 2021

Last updated: 18 February 2022

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1

Bréhin, P., J. Kozelka, and C. Bois. "Diammonium cyclopropane-1,1-dicarboxylate." Acta Crystallographica Section C Crystal Structure Communications 48, no. 11 (1992): 2094–96. http://dx.doi.org/10.1107/s0108270192006802.

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2

Schwarz, T., A. Petri, J. Schilling, and A. Lentz. "Hexaaquacobalt(II) Bis(hydrogen cyclopropane-1,1-dicarboxylate)." Acta Crystallographica Section C Crystal Structure Communications 54, no. 8 (1998): 1104–5. http://dx.doi.org/10.1107/s0108270198002960.

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3

Dubourg, A., E. Fabregue, L. Maury, and J. P. Declercq. "Structure of potassium hydrogen cyclopropane-1,1-dicarboxylate hemihydrate." Acta Crystallographica Section C Crystal Structure Communications 46, no. 8 (1990): 1394–96. http://dx.doi.org/10.1107/s0108270189013181.

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4

Illy, Nicolas, Sylvie Boileau, Mitchell A. Winnik, Jacques Penelle, and Valessa Barbier. "Thiol-ene “clickable” carbon-chain polymers based on diallyl cyclopropane-1,1-dicarboxylate." Polymer 53, no. 4 (2012): 903–12. http://dx.doi.org/10.1016/j.polymer.2011.12.047.

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5

Chagarovskiy, A. O., K. L. Ivanov, E. M. Budynina, O. A. Ivanova, and I. V. Trushkov. "Reaction of dimethyl (S)-2-(p-tolyl)cyclopropane-1,1-dicarboxylate with acetonitrile." Chemistry of Heterocyclic Compounds 48, no. 5 (2012): 825–27. http://dx.doi.org/10.1007/s10593-012-1062-7.

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6

Lee, Yu-Ting, Hang Thu Ta, and Ronald G. Duggleby. "Cyclopropane-1,1-dicarboxylate is a slow-, tight-binding inhibitor of rice ketol-acid reductoisomerase." Plant Science 168, no. 4 (2005): 1035–40. http://dx.doi.org/10.1016/j.plantsci.2004.11.020.

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7

Chagarovskiy, A. O., K. L. Ivanov, E. M. Budynina, O. A. Ivanova, and I. V. Trushkov. "ChemInform Abstract: Reaction of Dimethyl (S)-2-(p-Tolyl)cyclopropane-1,1-dicarboxylate with Acetonitrile." ChemInform 44, no. 8 (2013): no. http://dx.doi.org/10.1002/chin.201308106.

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8

Imamoto, T. "Samarium(II) iodide promoted reductive ring opening reaction of cyclopropane-1,1- dicarboxylic esters. Synthesis of substituted 5-pentanolides from carbonyl compounds and dimethyl cyclopropane-1,1-dicarboxylate." Tetrahedron Letters 35, no. 41 (1994): 7805–8. http://dx.doi.org/10.1016/s0040-4039(00)77377-1.

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9

Imamoto, Tsuneo, Toshihiko Hatajima, and Takeshi Yoshizawa. "Samarium(II) iodide promoted reductive ring opening reaction of cyclopropane-1,1-dicarboxylic esters. Synthesis of substituted 5-Pentanolides from carbonyl compounds and dimethyl cyclopropane-1,1-dicarboxylate." Tetrahedron Letters 35, no. 42 (1994): 7805–8. http://dx.doi.org/10.1016/0040-4039(94)80123-1.

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10

IMAMOTO, T., T. HATAJIMA, and T. YOSHIZAWA. "ChemInform Abstract: Samarium(II) Iodide Promoted Reductive Ring Opening Reaction of Cyclopropane-1,1-dicarboxylic Esters. Synthesis of Substituted 5- Pentanolides from Carbonyl Compounds and Dimethyl Cyclopropane-1,1- dicarboxylate." ChemInform 26, no. 12 (2010): no. http://dx.doi.org/10.1002/chin.199512095.

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11

Penelle, Jacques, and Tao Xie. "Ring-Opening Polymerization of Diisopropyl Cyclopropane-1,1-dicarboxylate under Living Anionic Conditions: A Kinetic and Mechanistic Study." Macromolecules 33, no. 13 (2000): 4667–72. http://dx.doi.org/10.1021/ma991173f.

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12

Jia, Lin, Ming Liu, Aurélie Di Cicco, et al. "Self-Assembly of Amphiphilic Liquid Crystal Polymers Obtained from a Cyclopropane-1,1-Dicarboxylate Bearing a Cholesteryl Mesogen." Langmuir 28, no. 30 (2012): 11215–24. http://dx.doi.org/10.1021/la301860b.

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13

Kitagawa, Osamu, Hiroki Fujiwara, and Takeo Taguchi. "Radical [3+2]-cycloaddition reaction with alkenes using dimethyl 2-(iodomethyl)cyclopropane-1,1-dicarboxylate as a new homoallyl radical precursor." Tetrahedron Letters 42, no. 11 (2001): 2165–67. http://dx.doi.org/10.1016/s0040-4039(01)00125-3.

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14

Gu, Xiangyong, Xiang Li, Yue Qu, Qi Yang, Pixu Li, and Yingming Yao. "Intermolecular Visible-Light Photoredox Atom-Transfer Radical [3+2]-Cyclization of 2-(Iodomethyl)cyclopropane-1,1-dicarboxylate with Alkenes and Alkynes." Chemistry - A European Journal 19, no. 36 (2013): 11878–82. http://dx.doi.org/10.1002/chem.201301943.

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15

Gu, Xiangyong, Xiang Li, Yue Qu, Qi Yang, Pixu Li, and Yingming Yao. "ChemInform Abstract: Intermolecular Visible-Light Photoredox Atom-Transfer Radical [3 + 2]-Cyclization of 2-(Iodomethyl)cyclopropane-1,1-dicarboxylate with Alkenes and Alkynes." ChemInform 45, no. 3 (2014): no. http://dx.doi.org/10.1002/chin.201403061.

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16

Kitagawa, Osamu, Hiroki Fujiwara, and Takeo Taguchi. "ChemInform Abstract: Radical [3 + 2]-Cycloaddition Reaction with Alkenes Using Dimethyl 2-(Iodomethyl)cyclopropane-1,1-dicarboxylate as a New Homoallyl Radical Precursor." ChemInform 32, no. 25 (2010): no. http://dx.doi.org/10.1002/chin.200125083.

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17

Novikov, Roman A., and Yury V. Tomilov. "Dimerization of Dimethyl 2-(Naphthalen-1-yl)cyclopropane-1,1-dicarboxylate in the Presence of GaCl3to [3+2], [3+3], [3+4], and Spiroannulation Products." Helvetica Chimica Acta 96, no. 11 (2013): 2068–80. http://dx.doi.org/10.1002/hlca.201200636.

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18

Liu, Jianping, Jie Wu, Xingxin Yu, and Guanyinsheng Qiu. "Synthesis of 2,3,4,11b-Tetrahydro-1H-pyridazino[6,1-a]isoquinolines via the Three-Component Reaction of 2-Alkynylbenzaldehydes, a Sulfonohydrazide and Dimethyl Cyclopropane-1,1-dicarboxylate." Synthesis 2011, no. 14 (2011): 2268–74. http://dx.doi.org/10.1055/s-0030-1260063.

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19

Yu, Xingxin, Guanyinsheng Qiu, Jianping Liu, and Jie Wu. "ChemInform Abstract: Synthesis of 2,3,4,11b-Tetrahydro-1H-pyridazino[6,1-a]isoquinolines via the Three-Component Reaction of 2-Alkynylbenzaldehydes, a Sulfonohydrazide and Dimethyl Cyclopropane-1,1-dicarboxylate." ChemInform 42, no. 47 (2011): no. http://dx.doi.org/10.1002/chin.201147147.

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20

Penelle, Jacques, Hugues Hérion, Tao Xie, and Pascal Gorissen. "Synthesis and characterization of a model carbon-chain polymer substituted by two esters on every third atom via anionic ringopening polymerization of a cyclopropane-1,1-dicarboxylate." Macromolecular Chemistry and Physics 199, no. 7 (1998): 1329–36. http://dx.doi.org/10.1002/macp.1998.021990710.

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21

Penelle, Jacques, Hugues Hérion, Tao Xie, and Pascal Gorissen. "Synthesis and characterization of a model carbon-chain polymer substituted by two esters on every third atom via anionic ring-opening polymerization of a cyclopropane-1,1-dicarboxylate." Macromolecular Chemistry and Physics 199, no. 7 (1998): 1329–36. http://dx.doi.org/10.1002/(sici)1521-3935(19980701)199:7<1329::aid-macp1329>3.0.co;2-k.

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22

Kitagawa, Osamu, Yoichiro Yamada, Atsushi Sugawara, and Takeo Taguchi. "Radical Cascade Reaction with 1,4-Dienes and 1,4-Enynes Using 2-(Iodomethyl)cyclopropane-1,1-dicarboxylate as a Homoallyl Radical Precursor: One-Step Synthesis of Bicyclo[3.3.0]octane Derivatives." ChemInform 33, no. 35 (2010): 74. http://dx.doi.org/10.1002/chin.200235074.

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23

Kitagawa, Osamu, Yoichiro Yamada, Atsushi Sugawara, and Takeo Taguchi. "Radical Cascade Reaction with 1,4-Dienes and 1,4-Enynes Using 2-(Iodomethyl)cyclopropane-1,1-dicarboxylate as a Homoallyl Radical Precursor: One-Step Synthesis of Bicyclo[3.3.0]octane Derivatives." Organic Letters 4, no. 6 (2002): 1011–13. http://dx.doi.org/10.1021/ol025583r.

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24

Elinson, Michail N., Sergey K. Feducovich, Anatolii N. Vereshchagin, Sergey V. Gorbunov, Pavel A. Belyakov, and Gennady I. Nikishin. "Electrocatalytic multicomponent cyclization of an aldehyde, malononitrile and a malonate into 3-substituted-2,2-dicyanocyclopropane-1,1-dicarboxylate—the first one-pot synthesis of a cyclopropane ring from three different molecules." Tetrahedron Letters 47, no. 51 (2006): 9129–33. http://dx.doi.org/10.1016/j.tetlet.2006.10.075.

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25

Novikov, Roman A., and Yury V. Tomilov. "ChemInform Abstract: Dimerization of Dimethyl 2-(Naphthalen-1-yl)cyclopropane-1,1-dicarboxylate (I) in the Presence of GaCl3to [3 + 2] (II), [3 + 3] (III), [3 + 4] (IV), and Spiroannulation Products (V)." ChemInform 45, no. 13 (2014): no. http://dx.doi.org/10.1002/chin.201413028.

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26

May, Nóra Veronika, Gyula Tamás Gál, Zsolt Rapi, and Péter Bakó. "Crystal structure of diethyl 3-(3-chlorophenyl)-2,2-dicyanocyclopropane-1,1-dicarboxylate." Acta Crystallographica Section E Crystallographic Communications 72, no. 2 (2016): 253–56. http://dx.doi.org/10.1107/s2056989016001444.

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Abstract:

In the racemic title compound, C17H15ClN2O4, which has been synthesized and the crystal structure of the solvent-free molecule determined, the angle between the planes of the benzene and cyclopropane rings is 54.29 (10)°. The molecular conformation is stabilized by two weak intramolecular C—H...Ocarboxylinteractions. In the crystal, C—H...O hydrogen bonds form centrosymmetric cyclicR22(10) dimers which are linked into chain substructures extending alongc. Further C—H...Nnitrilehydrogen bonding, including a centrosymmetric cyclicR22(14) association, link the chain substructures, forming a two-d

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27

Elinson, Michail N., Sergey K. Feducovich, Anatolii N. Vereshchagin, Sergey V. Gorbunov, Pavel A. Belyakov, and Gennady I. Nikishin. "Electrocatalytic Multicomponent Cyclization of an Aldehyde, Malononitrile and a Malonate into 3-Substituted-2,2-dicyanocyclopropane-1,1-dicarboxylate — The First One-Pot Synthesis of a Cyclopropane Ring from Three Different Molecules." ChemInform 38, no. 14 (2007). http://dx.doi.org/10.1002/chin.200714070.

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