Cyclopropyl-allyl rearrangement gem-dibromocyclopropanes under the action of aluminum carbenoides
- Autores: Yaroslavova A.V.1, Zosim T.P.1, Ramazanov I.R.1
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Afiliações:
- Institute of Petrochemistry and Catalysis of Russian Academy of Sciences
- Edição: Volume 61, Nº 5 (2025)
- Páginas: 538-543
- Seção: ЭКСПЕРИМЕНТАЛЬНЫЕ СТАТЬИ
- URL: https://journals.rcsi.science/0514-7492/article/view/318338
- DOI: https://doi.org/10.31857/S0514749225050033
- ID: 318338
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Resumo
Sobre autores
A. Yaroslavova
Institute of Petrochemistry and Catalysis of Russian Academy of Sciencesprosp. Oktyabrya, 141, Ufa, 450075 Russia
T. Zosim
Institute of Petrochemistry and Catalysis of Russian Academy of Sciences
Email: tania-ygnty@yandex.ru
prosp. Oktyabrya, 141, Ufa, 450075 Russia
I. Ramazanov
Institute of Petrochemistry and Catalysis of Russian Academy of Sciencesprosp. Oktyabrya, 141, Ufa, 450075 Russia
Bibliografia
- Thankachan A.P., Sindhu K.S., Krishnan K.K. Org. Biomol. Chem. 2015, 13, 8780–802. doi: 10.1039/c5ob01088h
- Doering E.W., Hoffmann A.K. J. Am. Chem. Soc. 1954, 76, 6162–6165. doi: 10.1021/ja01652a087
- Kostikov R.R., Molcahnov A.P. Top. Curr. Chem. 1990, 155, 41.
- Fedoryński M. Chem. Rev. 2003, 103, 1099–1132. doi: 10.1002/chin.200326275
- Murphy J.A., Scott K.A., Sinclair R.S., Lewis N. Tetrahedron Lett. 1997, 38, 7295–7298. doi: 10.1016/S0040-4039(97)01695-X
- Murphy J.A., Scott K.A., Sinclair R.S., Martin C.G., Kennedy A.R., Lewis N. J. Chem. Soc., Perkin Trans. 1. 2000, 15, 2395–2408. doi: 10.1039/b002565h
- Trost B.M., Oslob J.D. J. Am. Chem. Soc. 1999, 121, 13, 3057–3064. doi: 10.1021/ja983617d
- Sydnes L.K., Mungaroo R., Aanesen B.A. Acta Chem. Scand. 1998, 52, 1386–1391. doi: 10.3891/acta.chem.scand.52-1386
- Banwell M.G., Reum M.E. Advances in Strain in Organic Chemistry. JAI Press. 1991, 1, 19.
- Nerdel F., Buddrus J. Tetrahedron Lett. 1965, 6, 3197–3198. doi: 10.1016/S0040-4039(01)89211-X
- Skattebоl L., Boulette B. J. Org. Chem. 1966, 31, 81–85. doi: 10.1021/jo01339a016
- Ramazanov I.R., Yumagulova A.V., Dzhemilev U.M., Nefedov O.M. Tetrahedron Lett. 2009, 50, 4233–4235. doi: 10.1002/chin.200944057
- Kadikova R.N., Ramazanov I.R., Zosim T.P., Yaroslavova A.V., Dzhemilev U.M. Tetrahedron Lett. 2015, 71, 3290–3295. doi: 10.1016/j.tet.2015.03.113
- Ramazanov I.R., Yaroslavova A.V., Dzhemilev U.M. Tetrahedron Lett. 2016, 57, 4024–4026. doi: 10.1016/j.tetlet.2016.07.043
- Ramazanov I.R., Kadikova R.N., Zosim T.P., Dzhemilev U.M., de Meijere A. Eur. J. Org. Chem. 2017, 47, 7060–7067. doi: 10.1002/ejoc.201700991
- Ramazanov I.R., Yaroslavova A.V., Yaubasarov N.R., Dzhemilev U.M. Synlett. 2018, 29, 627–629. doi: 10.1055/s-0036-1591731
- Frisch M.J., Trucks G.W., Schlegel H.B., Scuseria G.E., Robb M.A., Cheeseman J.R., Scalmani G., Barone V., Petersson G.A., Nakatsuji H., Li X., Caricato M., Marenich A. V., Bloino J., Janesko B.G., Gomperts R., Mennucci B., Hratchian H.P., Ortiz J.V., Izmaylov A.F., Sonnenberg J.L., Williams-Young D., Ding F., Lippari- ni F., Egidi F., Goings J., Peng B., Petrone A., Henderson T., Ranasinghe D., Zakrzewski V.G., Gao J., Re- ga N., Zheng G., Liang W., Hada M., Ehara M., Toyo- ta K., Fukuda R., Hasegawa J., Ishida M., Nakajima T., Honda Y., Kitao O., Nakai H., Vreven T., Throssell K., Montgomery J.A.Jr., Peralta J.E., Ogliaro F., Bear- park M.J., Heyd J.J., Brothers E.N., Kudin K.N., Sta- roverov V.N., Keith T.A., Kobayashi R., Normand J., Raghavachari K., Rendell A.P., Burant J.C., Iyengar S.S., Tomasi J., Cossi M., Millam J.M., Klene M., Adamo C., Cammi R., Ochterski J.W., Martin R.L., Morokuma K., Farkas O., Foresman J.B., Fox D.J. Gaussian 16, Revision B.01. Gaussian, Inc., Wallingford CT, 2016.
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