Моделирование механизмов многомаршрутных каталитических реакций формирования и разрыва связей углерод-углерод (1090302), страница 28
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Bicyclo[2.2.1]hepta-2,5-diene (Norbornadiene). / T.J. Kettles, W.Tam // e-EROS Encyclopedia of Reagents for Organic Synthesis. – 2012.72. Klumpp, G.W. Homo-1,4-addition of dichlorocarbene and dibromocarbene tonorbornadienes /G.W. Klumpp, P.M. Kwantes // Tetrahedron Lett. – 1976. – V.17. –P. 707-710.73. Lautens, M.
Nickel-catalyzed [2.pi. + 2.pi. + 2.pi.] (homo-Diels-Alder) and[2.pi.+ 2.pi.] cycloadditions of bicyclo[2.2.1]hepta-2,5-dienes /M. Lautens, L.E.Edwards, W. Tam, A.J. Lough // J. Am. Chem. Soc. – 1995. – V.117. – P. 1027610291.24874. Trost, B.M. Palladium-mediated cycloaddition approach to cyclopentanoids.Introduction and initial studies /B.M. Trost, D.M.T. Chan // J. Am.
Chem. Soc. –1983. – V.105. – P. 2315-2325.75. Binger, P. Cyclopropenes and methylenecylopropanes as multifunctional reagentsin transition metal catalyzed reactions /P. Binger, H.M. Buch // Top. Curr. Chem. –1987. – V.135. – P. 77-151.76.Villeneuve,K.Asymmetricinductioninruthenium-catalyzed[2+2]cycloadditions between bicyclic alkenes and a chiral acetylenic acyl sultam /K.Villeneuve, W. Tam // Angew.
Chem., Int. Ed. – 2004. – V.43, I.5. – P. 610-613.77. Riddell, N. Ruthenium-catalyzed [2+2] cycloadditions of alkynyl sulfides andalkynyl sulfones /N. Riddell, W. Tam // J. Org. Chem. – 2006. – V.71. – P. 19341937.78. Burton, R.R. Study on the reactivity of oxabicyclic alkenes in rutheniumcatalyzed [2+2] cycloadditions /R.R. Burton, W. Tam // J. Org. Chem.
– 2007. –V.72. – P. 7333-7336.79. Allen, A. Alkynyl halides in ruthenium(II)-catalyzed [2+2] cycloadditions ofbicyclic alkenes /A.Allen, K. Villeneuve, N. Cockburn, E. Fatila, N. Riddell, W. Tam// Eur. J. Org. Chem. – 2008. – V.2008. – P. 4178-4192.80.Hanaoka,M.Bis(cyclopentadienyl)tetracarbonyldimolybdenum-alkynecomplexes mediated [2 + 2 + 1] cycloaddition: the formation of 3-substitutedcyclopentenone derivatives /M. Hanaoka, C. Mukai, M. Ushiyama // J. Chem. Soc.,Chem. Commun. – 1992.
– I.14. – P. 1014-1015.81. Mayo, P. Remote substituent effects on regioselectivity in the Pauson-Khandreaction of 2-substitued norbornenes /P. Mayo, W. Tam // Tetrahedron. – 2001. – V.57. – P. 5943-5952.82. Kim, J.-Y. Synthesis and structure–activity studies of novel homomorpholineoxazolidinone antibacterial agents /J.-Y. Kim, F.E. Boyer, A.L. Choy, M.D. Huband,P. J. Pagano, J.V.N. Vara Prasad // Bioorg. Med. Chem. Lett. – 2009.
– V.19, I.2. – P.550-553.24983. Gugelchuck, M.M. Kinetic and modeling studies on the nickel-catalyzed homodiels-Alder addition of 7-substituted norbornadienes /M.M. Gugelchuck, A.L.Doherty-Kirby // J. Org. Chem. – 1996. – V.61. – P. 3490-3495.84. Lautens, M. Cobalt-catalyzed [2.pi. + 2.pi. + 2.pi.] (Homo-Diels-Alder) and [2.pi.+ 2.pi. + 4.pi.] cycloadditions of bicyclo[2.2.1]hepta-2,5-dienes / M. Lautens, W.Tam, J.C. Lautens, L.G.
Edwards, C.M. Crudden, A.C. Smith // J. Am. Chem. Soc. –1995. – V.117. – P. 6863-6879.85. Chen, Y. Metal-catalyzed [4 + 2 + 2] cycloadditions: cycloadducts of substitutednorbornadienes and their opening with Zeise's dimer /Y.Chen, J.K. Snyder // J. Org.Chem. – 1998. – V.63. – P. 2060-2061.86. Ma, B. Development of a new cobalt catalyst system for the [4 + 2 + 2]cycloadditions of functionalized norbornadienes and butadiene / B.
Ma, J.K. Snyder //Organometallics. – 2002. – V. 21. – P. 4688-4695.87. Scrauzer, G.N. Über die katalytische Anlagerung von Olefinen und Alkinen anNorbornadien mit Ni0-Verbindungen und einem neuen NiII-Komplex /G.N.Scrauzer, P. Glockner // Chem. Ber. – 1964. – V.97, I.9 – P. 2451-2462.88. Turecek, F. 6+2 cycloadditions catalysed by titanium complexes II /F. Turecek,K. Mach, H. Antropiusova, L. Petrusova, V. Hanus, P. Sedmera // Tetrahedron. –1984. – V.40.
– P. 3295-3302.89. Myers, H.K. Vinyl nortricyclane. / H.K. Myers, J.E. Lyons, A. Schneider // USPatent 4098835. – 1978. – App. No.: 829301. – CI: C07C 015/00.90.Bogdanoke,B.Assymmetrishesynthesenmithomogenenubergargsmetallkatalysatoren /B. Bogdanoke, B. Henc, A. Losler, B. Meister, H.Pauling, G. Wilke // Angew. Chem. – 1973. – V.85. – P. 1013-1023.91. Myers, H.K. Catalytic codimerization of norbornadiene with acrylonitrile. / H.K.Myers, A.
Schneider // US Patent 4107198. – 1978. – App. No.: 812208. – CI: C07C120/00, C07C 121/46.25092. Schneider, A. Catalytic codimerization of norbornadiene with an acrylic acidester. / A. Schneider, H.K. Myers // US Patent 4139714. – 1979. – App. No.: 812206.– CI: C07C 069/74.93. Schneider, A. Catalytic codimerization of norbornadiene with an acrylic acidester. / A.
Schneider, H.K. Myers // US Patent 4142055. – 1979. – App. No.: 812207.– CI: C07C 069/74.94. Noyori, R. Nickel (0) catalyzed reaction of quadricyclane with electron deficientolefins /R. Noyori, I. Umeda, H. Kawauchi, H. Takaya // J. Am. Chem. Soc. – 1975.– V.97. – P.
812-819.95. Pardigon, O. Influence of aluminum Lewis acids on the diastereoselectivity of thenickel-catalyzed [2+2+2] cycloaddition of norbornadiene and electron deficientalkenes /O. Pardigon, A. Tenaglia, G. Buono // Tetrahedron Lett. ‒ 2000. ‒ V.41. –P.4089-409296. Lautens, M. Stereoselectivity in the Homo Diels-Alder Reaction.
/M. Lautens,L.G. Edwards // Tetrahedron Lett. – 1989. – V.30. – P. 6813-6816.97. Дмитриев, Д.В. Содимеризация норборнадиена с активированнымиолефинами: дис. … канд. хим. наук: 02.00.04 / Дмитриев ДмитрийВикторович.‒ М., 2005. ‒ 130 с.98. Noyori, R. Transition metall catalysed [2+2] cross-addition of olefins. Ni(0) –catalyzed cycloaddition of norbornadiene and methylencyclopropane /R.
Noyori, T.Ishigumi, N. Hayashi, H. Takaya // J. Amer .Chem. Soc.– 1973.– V.95, I.5.– P. 16741676.99. Ullman, E.F. // Chem. and Ind. ‒ 1958. ‒ V.81. ‒ P. 1173-1174.100.Greco,A.Catalyticnorbornadiene-butadieneandnorbornadiene-1.1-dimethylallene codimerization / A. Greco, A. Carbonaro, G. Dall’Asta // J. Org.Chem. – 1970. – V.35. – P. 271-274.101. Myers, H.K. Preparation of tetramethylene nortricyclane. / H.K. Myers, A.Schneider // US Patent 4152360. – 1979. – App.
No.: 819443. – CI: C07C 013/28.251102. Carbonaro, A. Catalitic behaviour of some Ziegler-Natta catalysts in thenorbornadiene-butadiene codimerization /A. Carbonaro, F. Cambisi, G. Dall’Asta // J.Org. Chem. – 1971. – V.36. – P. 1443-1445.103. Chen, Y. Metal-сatalyzed [4 + 2 + 2] сycloadditions: сycloadducts of substitutednorbornadienes and their opening with zeise's dimer /Y. Chen, J.K.
Snyder // J. Org.Chem. – 1998. – V.63, I.7. – P. 2060-2061.104. Chen, Y. Transition metal-catalyzed [4 + 2 + 2] cycloadditions ofbicyclo[2.2.1]hepta-2,5-dienes (norbornadienes) and bicyclo[2.2.2]octa-2,5-dienes/Y. Chen, R. Kiattansakul, B.
Ma, J.K. Snyder // J. Org. Chem. – 2001. – V.66, I.21.– P. 6932 – 6942.105. Heimbach, P. Mischoligomerisation von butadiene mit bicyclo[2.2.1]hept-2enen /P. Heimbach, R. Meyer, G. Wilke // Liebigs Ann. Chem. – 1975. – V.1975, I.4. – P. 743-751.106. Lautens, M. Regiochemical control in the Homo-Diels-Alder reaction:substituent effects /M. Lautens, L.G. Edwards // J. Org. Chem.
– 1991. – V.56, I.12. –P. 3761-3763.107. Lautens, M. Stereoselectivity in the homo-Diels-Alder reaction: effect of aremote 7-substituent on nickel-catalysed cycloadditions /M. Lautens, W. Tam, L.G.Edwards // J. Chem. Soc., Perkin Trans.1. – 1994.
– V.15. – P. 2143-2150.108. Takaya, H. Ni(0) catalyzed cross-addition of bicyclo[2.2.1]heptene derivativeswith electron –deficient olefins /H. Takaya, M. Yamakawa, R. Noyori // Bull. Chem.Soc. Jpn. – 1982. – V.55. – P. 852-855.109. Дмитриев, Д.В. Каталитические синтезы полициклических соединений наоснове норборна-2,5-диена в присутствии комплексов никеля.
Сообщение 4.Вопросы региоселективности в реакциях содимеризации норборнадиена сактивированными олефинами. /Д.В. Дмитриев, О.С. Манулик, В.Р. Флид //Кинетика и катализ. – 2004. – T.45. – С. 181-187.252110. Эфрос, И.Е. Никель-катализируемые реакции циклоприсоединенияактивированных олефинов к норборнадиену: дис. … канд. хим. наук: 02.00.04 /Эфрос Илья Евгеньевич. ‒ М., 2010.
‒ 133 с.111. Kalnes, T.N. Green Diesel: A Second Generation Biofuel./ T.N. Kalnes, T.Marker, D.R. Shonnard // Int. J. of Chem. Reactor Engineering. – 2007. – V.5, I.1. –A48.112. Мировые инвестиции в «зеленую» энергетику выросли на 32%[Электронный ресурс] / Информационно-аналитическое агентство Cleandex. –2011.–Режимдоступа:http://www.cleandex.ru/articles/2011/07/08/Mirovye_investitsii_v_zelenuyu_energetiku_vyrosli.113. Smith, B. Catalytic upgrading of tri-glycerides and fatty acids to transportbiofuels /B. Smith, H.C. Greenwell, A. Whiting // Energy Environ. Sci.
– 2009. – V.2.– P. 262-271.114. Яковлев, В.А. Гетерогенные катализаторы процессов превращениятриглицеридов жирных кислот и их производных в углеводороды топливногоназначения /В.А. Яковлев, С.А. Хромова, В.И. Бухтияров // Успехи химии. –2011. – Т.80, №10. – С. 955-970.115. Кацер, Д.В. Производство биодизельного топлива. Мировой опыт иперспективы производства в республике Беларусь [Электронный ресурс] / Д.В.Кацлер // Белорусская государственная сельскохозяйственная академия. – 2009.– Режим доступа: http://www.bioethanol.ru/Legislation/belarus/.116.
Statistics [Электронный ресурс] / European Biodiesel Board. –2011. – Режимдоступа: http://www.ebb-eu.org/stats.php.117. New capacity on stream [Электронный ресурс] / Neste Oil. –2011. – Режимдоступа: http://www.nesteoil.com/default.asp?path=1,41,11991,12243,13565.118. U.S. Census releases 2010 biodiesel production estimates [Электронныйресурс]/BiodieselMagazine.–2011.–Режимдоступа:http://biodieselmagazine.com/articles/7658/u-s-census-releases-2010-biodieselproduction-estimates.253119. Водоросли для биодизеля: новая жизнь и заброшенные исследования(Часть 1) [Электронный ресурс] / Paskalex: Новости биодизеля.
– 2011. – Режимдоступа: http://paskalex.blogspot.com/2009/11/1.html.120. Schenk, P.M. Second generation biofuels: High-efficiency microalgae forbiodiesel production /P.M. Schenk, S.R. Thomas-Hall, E. Stephens, U.C. Marx, J.H.Mussgnug, C. Posten, O. Kruse, B. Hankamer // BioEnergy Research.
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