Дизайн и синтез металлоценов 4 группы - эффективных прекатализаторов гомо - и сополимеризации алкенов (1098265), страница 79
Текст из файла (страница 79)
Wennerstrom // Acta Chem. Scand. - 1979. V. B33. - № 4. - P. 307-308.162. Wilkinson, G. [текст] / G. Wilkinson, T. S. Piper // J. Inorg. Nucl. Chem. - 1956. - V. 2. - № 1. P. 32-37.163. Acheson, R. M. Experiments bearing on the synthesis of cortisone. Part I. Some cyclopentenonederivatives [текст] / R. M. Acheson, R. Robinson // J. Chem. Soc. - 1952. - P. 1127-1133.164. Пат. США US5763664, МПК C07C45/66; C07C45/83; C07C49/597; (IPC1-7): C07C49/105.Process for preparing cyclopentenones [текст] / Saunders P. C.
(США); заявитель ALBEMARLECORP; заявл. 01.12.1995 ; опубл. 09.06.1998. - 3 с. : илл.165. Borsche, W. Studien in der Gruppe des Phenyl-cyclopentans [текст] / W. Borsche, W. Menz //Chem. Ber. - 1908. - B. 41. - № 1 - S. 190-210.166. Plattner, P. A.
Transformation d'acides aliphatiques non sature's en cyclopente'nones [текст] / P.A. Plattner, A. S. Pfau // Helv. Chim. Acta. - 1937. - B. 20. - № 1. - S. 1474-1483.167. Ansell, M. F. Reduced cyclic compounds. Part IV. The intramolecular acylation of some olefinicacids [текст] / M. F. Ansell, S. S. Brown // J. Chem. Soc. - 1958. - P. 2955-2961.168.
Eaton, P. E. Phosphorus pentoxide-methanesulfonic acid. A convenient alternative to polyphosphoric acid [текст] / P. E. Eaton, G. R. Carlson, J. T. Lee // J. Org. Chem. - 1973. - V. 38. - № 25. - P.4071-4073.169. Elliott, M. 435. The preparation of cyclopentenones from the products of stobbe condensationswith aliphatic ketones [текст] / M. Elliott // J. Chem. Soc. - 1956. - P. 2231-2241.170.
Frank, R. L. The Synthesis of Octahydrocoumarins and their Reaction with Phosphorus Pentoxide [текст] / R. L. Frank, R. C. Pierle // J. Am. Chem. Soc. - 1951. - V. 73. - № 2. - P. 724-730.171. Dev, S. [текст] / S. Dev // J. Indian Chem. Soc. - 1957. - V. 34. - P. 178-181.172. de Vreis, L. Preparation of 1,2,3,4,5-Pentamethyl-cyclopentadiene, 1,2,3,4,5,5-Hexamethylcyclopentadiene, and 1,2,3,4,5-Pentamethyl-cyclopentadienylcarbinol [текст] / L. de Vreis // J. Org.Chem. - 1960. - V.
25. - № 10. - P. 1838.173. Denmark, S. E. Silicon-directed Nazarov cyclization [текст] / S. E. Denmark, T. K. Jones // J.Am. Chem. Soc. - 1982. - V. 104. - № 9. - P. 2642-2649.375174. Hiyama, T. Regio- and stereoselective cyclopentenone annulation by means of ketone-propargylalcohol adducts [текст] / T.
Hiyama, M. Shinoda, H. Nozaki // J. Am. Chem. Soc. - 1979. - V. 101. № 6. - P. 1599-1600.175. Conia, J. M. No.515 - Sur la preparation de cyclopentenones par adtion de l'acide polphosphorique ssur les esters d'acides α-ethyleniques. 1 Parte: Aspects pratiques [текст] / J. M. Conia, M. L.Leriverend // Bull.
Soc. Chim. Fr. - 1970. - № 8-9. - P. 2981-2991.176. Dev, S. [текст] / Dev S. // J. Indian Chem. Soc. - 1957. - V. 34. - № 1. - P. 169-173.177. / Hacini, S. A facile route to cyclopentenones by Friedel-Crafts acylation [текст] / S. Hacini, R.Pardo, M. Santelli A // Tetrahedron Lett.
- 1979. - № 47. - P. 4553-4556.178. Austin, R. N. Synthesis and properties of novel substituted 4,5,6,7-tetrahydroindenes and selected metal complexes [текст] / R. N. Austin, T. J. Clark, T. E. Dickson, C. M. Killian, T. A. Nile,D. J. Schabacker, A. T. McPhail // J. Organomet. Chem. - 1995. - V. 491. - № 1-2. - P. 11-18.179. Hiyama, T. Acid-catalyzed reaction of dichlorocyclopropylcarbinols [текст] / T. Hiyama, M.Tsukanaka, H. Nozaki // J.
Am. Chem. Soc. - 1974. - V. 96. - № 11. - P. 3713-3714.180. Fendrick, C. M. Large-scale synthesis of 1,2,3,4,5-pentamethylcyclopentadiene [текст] / C. M.Fendrick, L. D. Schertz, E. A. Mintz, T. J. Marks, T. E. Bitterwolf, P. A. Horine, T. L. Hubler, J. A.Scheldon, D. D. Belin // Inorg.
Synth. - 1992. - № 29. - P. 193-198.181. Staudinger, H. Insektentötende Stoffe V. Synthese des Tetrahydro-pyrethrons, des Reduktionsproduktes des Pyrethrolons [текст] / H. Staudinger, L. Ruzicka // Helv. Chim. Acta. - 1924. - B. 7. № 1. - S. 245.182. Bachmann, W. E. The Synthesis of Compounds Related to the Sex Hormones [текст] / W.
E.Bachmann, R. D. Morin // J. Am. Chem. Soc. - 1944. - V. 66. - № 4. - P. 553-557.183. Gordon, A. R. Mild and Efficient N-Oxide Promoted Pauson-Khand Reactions with Ethylene[текст] / A. R. Gordon, C. Johnstone, W. A. Kerr // Synlett. - 1995. - № 10. - P. 1083-1084.184. Lee, B. Y.
Promoters for the (alkyne) hexacarbonyldicobalt-based cyclopentenone synthesis[текст] / B. Y. Lee, Y. K. Chung, N. Jeong, M. Heudecek, P. L. Pauson // Organometallics. - 1993. V. 12. - № 1. - P. 220-223.185. Lee, B. Y. Generation of Cyclopentadienyl Ligands via the Pauson-Khand and Retro-Diels-AlderReactions [текст] / B. Y. Lee, H. Moon, Y. K. Chung, N. Jeong // J. Am. Chem. Soc. - 1994. - V.116. - № 5. - P. 2163-2164.186.
Kang, Y. K. Synthesis of fulvalene-bridged bimetallic compounds containing a substituted cyclopentadienyl group based on Pauson-Khand chemistry [текст] / Y. K. Kang, K. S. Shin, S. G. Lee,I. S. Lee, Y. K. Chung // Organometallics. - 1999. - V. 18. - № 2. - P. 180-186.376187. Saltiel, J. A case of fully diffusion-controlled exothermic triplet excitation transfer [текст] / J.Saltiel, P. T. Shannon, O. C.
Zafiriou, A. K. Uriarte // J. Am. Chem. Soc. - 1980. - V. 102. - № 22. P. 6799-6808.188.Evans,W.J.Synthesisandreactivityofatethereddienecyclopentadiene,(C5Me4H)SiMe2(CH2CH=CHCH=CH2), and its alkali metal salts [текст] / W. J. Evans, D. G.Giarikos, J. W. Ziller // J. Organomet. Chem. - 2003.
- V. 688. - № 1-2. - P. 200-205.189. Arias, J. L. Stable catalyst for intermolecular Pauson–Khand reaction [текст] / J. L. Arias, A.Cabrera, P. Sharma, N. Rosas, R. Sampere // J. Mol. Catal., A: Chem. - 2006. - V. 246. - № 1-2. - P.237-241.190. Lee, B. Y. Synthesis of bis(1.2.3-substituted cyclopentadientl)zirconium derivatives and their usein ethylene polymerization [текст] / B. Y. Lee, J.
W. Han, Y. K. Chung, S. W. Lee // J. Organomet.Chem. - 1999. - V. 587. - № 2. - P. 181-190.191. Shibata, T. Iridium-Chiral Diphosphine Complex Catalyzed Highly Enantioselective PausonKhand-Type Reaction [текст] / T. Shibata, K. Takagi // J. Am. Chem. Soc. - 2000. - V.
122. - № 40. P. 9852-9853.192. Chung, Y. K. Transition metal alkyne complexes: the Pauson-Khand reaction [текст] / Y. K.Chung // Coord. Chem. Rev. - 1999. - V. 188. - № 1. - P. 297-341.193. Kim, M. W. Group 4 metallocene complexes with annulated twelve-membered ring cyclopentadienyl ligands: their synthesis, characterization and catalytic behaviour in olefin polymerization[текст] / M. W. Kim, E.
Hong, T. K. Han, S. I. Woo, Y. Do // J. Organomet. Chem. - 1996. - V. 523.- № 2. - P. 211-219.194. Polo, E. Synthesis of ring-substituted bis-η5-cyclopentadienyl derivatives of the group IV elements containing the bicyclic ligands η5-C5H3(1,2-CH2-)n, n = 4,5, or 6 [текст] / E. Polo, R. M. Bellabarba, G. Prini, O. Traverso, M.
L. H. Green // J. Organomet. Chem. - 1999. - V. 577. - № 2. - P.211-218.195. Lee, B. Y. Preparation of a cyclopentadienyl ligand from the Pauson-Khand reaction product andits use in complex chemistry [текст] / B. Y. Lee, H. Moon, Y. K. Chung, N. Jeong, G. B. Corpenter //Organometallics. - 1993. - V. 12. - № 10. - P. 3879-3884.196. Пат. США US2006252895, МПК B01J31/00; B01J31/22; C07B61/00; C07C1/207; C07C13/54;C07C13/547; C07C13/567; C07C2/86; C07C45/46; C07C49/643; C07C49/675; C07F17/00;C07F7/08; C08F10/00; C08F4/44; C08F4/622; C08F4/64; C08F4/642; C08F4/6592. Metallocenecompounds and use thereof in catalysts for the polymerization of olefins [текст] / Bishop C., JonesR., Raman K., Dang Vu.
A., Dang L. C., Resconi L., Dall T. Occo, Galimberti M. (Италия); заявитель BASELL TECHNOLOGY CO BV; заявл. 06.04.1994 ; опубл. 09.11.2006. - 14 с. : илл.377197. Imafuku, K. A Simple and Convenient Synthesis of 5-Alkyl-Substituted 3-Isopropenyl- and 3Acetyltropolones [текст] / K. Imafuku, K. Arai // Synthesis. - 1989. - № 7. - P. 501-505.198. Erden, I. Scope and limitations of fulvene synthesis. Preparation of 6-vinyl-substituted and finctionalized fulvenes. First examples of nucleophilic substitution on a 6-(chloromethyl)fulvene[текст] / I. Erden, F.
P. Xu, A. Sadoun, W. Smith, G. Sheff, M. Ossun // J. Org. Chem. - 1995. - V.60. - № 4. - P. 813-820.199. Пат. США US3192275, МПК C07C2/86 Process for making fulvenes [текст] / Friesleben W.(Германия); заявитель CONSORTIUM ELEKTROCHEM IND;заявл. 01.09.1961 ; опубл.29.06.1965. - 3 с. : илл.200. Clark, T. J. Regioselective synthesis of dialkyl-1,3-cyclopentadienes via novel 2-alkyl-6,6dialkylfulvenes [текст] / T. J. Clark // Synlett. - 1990.
- № 10. - P. 589-590.201. Miller, S. A. Isotactic-Hemiisotactic Polypropylene from C1-Symmetric ansa-Metallocene Catalysts: A New Strategy for the Synthesis of Elastomeric Polypropylene [текст] / S. A. Miller, J. E.Bercaw // Organometallics. - 2002. - V. 21. - № 5. - P. 934-945.202. Alt, H. G. o-Phenylalkyl substituted amido functionalized ansa half-sandwich complexes of titanium and zirconium and metallacycles thereof as catalyst precursors for homogeneous ethylene polymerization [текст] / H. G. Alt, A. Reb, K.
Kundu // J. Organomet. Chem. - 2001. - V. 628. - № 2. P. 211-221.203. Abrams, M. B. Fluxional η3-allyl derivatives of ansa-scandocenes and an ansa-yttrocene. Measurements of the berriers for the η3 to η1 process as an indicator of olefin binding energy to d0 metallocenes [текст] / M. B. Abrams, J. C. Yoder, C. Loeber, M. W. Day, J. E. Bercaw // Organometallics.- 1999.
- V. 18. - № 8. - P. 1389-1401.204. Hoffmann, H. M. R. Regioselective Preparation of Vinylcyclopentadienes and Selected Cycloadditions [текст] / H. M. R. Hoffmann, O. Koch // J. Org. Chem. - 1986. - V. 51. - № 15. - P.2939-2944.205. Hafner, K. 6-(Dimethylamino)fulvene [текст] / K. Hafner, K. H. Vopel, G. Ploss, C. Konig //Organic Syntheses. - 1967. - V. 47. - P.
52-53.206. Wade, L. G. Cyclodehydratation reaction using molted sodium tetrachloroaluminate [текст] / L.G. Wade, K. J. Acker, R. A. Earl, R. A. Osteryoung // J. Org. Chem. - 1979. - V. 44. - № 21. - P.3724-3725.207. Boykin, D. W. 17O NMR stadies on alkylindanones: steric effects [текст] / D. W. Boykin, R.
![](https://s.studizba.com/z.php?f=/templates/si/i/noavatar.png&w=100&h=100&t=1"){kind=avatar}
