Subscribe to RSS
DOI: 10.1055/s-2007-983890
Synthesis of Organosilatranes via Rhodium(I)-Catalyzed Silylation of Organic Iodides with Hydrosilatrane
Publication History
Publication Date:
11 September 2007 (online)
Abstract
The silylation of aryl and alkenyl iodides with hydrosilatrane in the presence of a rhodium(I) catalyst and DABCO provides the corresponding organosilatranes in good yield. The same catalyst system also enables the related coupling of hydrogermatrane.
Key words
silicon - rhodium - catalysis - cross-coupling - halides
-
1a
Voronkov MG.D’yakov VM.Kirpichenko SV. J. Organomet. Chem. 1982, 233: 1 -
1b
Verkade JK. Coord. Chem. Rev. 1994, 137: 233 -
1c
Pestunovich V.Kirpichenko S.Voronkov M. In The Chemistry of Organic Silicon Compounds Part 1, Vol. 2:Rappoport Z.Apeloig Y. Wiley; Chichester: 1998. p.1447-1537 - 2
Karlov SS.Zaitseva GS. Chem. Heterocycl. Compd. (Engl. Transl.) 2001, 37: 1325 - 3
Riggleman S.DeShong P. J. Org. Chem. 2003, 68: 8106 - 4
Faller JW.Kultyshev RG. Organometallics 2002, 21: 5911 -
5a
Frye CL.Vogel GE.Hall JA. J. Am. Chem. Soc. 1961, 83: 996 -
5b
Frye CL.Vincent GA.Finzel WA. J. Am. Chem. Soc. 1971, 93: 6805 -
7a
Murata M.Suzuki K.Watanabe S.Masuda Y. J. Org. Chem. 1997, 62: 8569 -
7b
Manoso AS.DeShong P. J. Org. Chem. 2001, 66: 7449 -
8a
Murata M.Ishikura M.Nagata M.Watanabe S.Masuda Y. Org. Lett. 2002, 4: 1843 -
8b
Murata M.Yamasaki H.Ueta T.Nagata M.Ishikura M.Watanabe S.Masuda Y. Tetrahedron 2007, 63: 4087 - 9
Faller JW.Kultyshev RG. Organometallics 2003, 22: 199 - 11
Murata M.Watanabe S.Masuda Y. Tetrahedron Lett. 1999, 40: 9255 - 12
Nakamura T.Kinoshita H.Shinokubo H.Oshima K. Org. Lett. 2002, 4: 3165
References
Kishida, E.; Saiki, T.; Ishiyama, T.; Miyaura, N. The 53rd Symposium on Organometallic Chemistry; Osaka, Japan, September 8-9, 2006; Abstract PB253.
10The results of the silylation of ethyl 4-iodobenzoate with hydrosilatrane (1) in the presence of [Rh(cod)(MeCN)2]BF4 and DABCO in selected solvents are as follows [% NMR yield (% conversion)]: DMF, 63 (100); DMSO, 0 (100); MeCN, 0 (100); dioxane, 38 (100); DCE, 0 (8); toluene, trace (27).
13To some extent, a plausible mechanism for the case of triethoxysilane, proposed by us (see ref. 8b), would refer to the present situation.