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Journal of Organometallic Chemistry

Volumn 689, Issue 10, 2004, Pages 1856-1859

Tris(trimethylsilylmethyl)alane: An aldehyde selective peterson methylenation reagent

(2) Abedi, Vahak a Battiste, Merle A a

a University of Florida (United States)

Author keywords

Aldehyde vs. ketone selectivity; Peterson methylenation; Tris(trimethylsilylmethyl)alane

Indexed keywords

ALCOHOL DERIVATIVE; ALDEHYDE DERIVATIVE; ALLYLTRIMETHYLSILANE; CYCLOHEXANONE DERIVATIVE; FLUORENONE DERIVATIVE; INDANONE DERIVATIVE; ORGANOHALOGEN DERIVATIVE; ORGANOLITHIUM COMPOUND; ORGANOSILICON DERIVATIVE; REAGENT;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL MODIFICATION; CHEMICAL REACTION KINETICS; CHEMICAL STRUCTURE; CONTROLLED STUDY; SILYLATION; SYNTHESIS;

EID: 1842843023 PISSN: 0022328X EISSN: None Source Type: Journal
DOI: 10.1016/j.jorganchem.2004.02.009 Document Type: Short Survey

Times cited : (3)

References (14)

1
- 0002469552
- For a comprehensive survey of reagents and conditions related to the title reactions see
- For a comprehensive survey of reagents and conditions related to the title reactions see: Pine S.H. Org. React. 43 1993 1
- (1993) Org. React. , vol.43 , pp. 1
- Pine, S.¹

2
- 0002974335
- Ager D.J. Org. React. 38 1988 1
- (1988) Org. React. , vol.38 , pp. 1
- Ager, D.J.¹

3
- 0002342369
- Kauffman T. King R. Tetrahedron Lett. 22 1981 5031
- (1981) Tetrahedron Lett. , vol.22 , pp. 5031
- Kauffman, T.¹ King, R.²

4
- 0010626350
- Ethyl Corporation
- G. Bruno, The Use of Aluminum Alkyls in Organic Synthesis, Ethyl Corporation, 1970
- (1970) The Use of Aluminum Alkyls in Organic Synthesis
- Bruno, G.¹

5
- 1842848857
- Ethyl Corporation
- G. Bruno, The Use of Aluminum Alkyls in Organic Synthesis (Suppl. 1), Ethyl Corporation, 1973
- (1973) The Use of Aluminum Alkyls in Organic Synthesis , Issue.SUPPL. 1
- Bruno, G.¹

6
- 1842870864
- Ethyl Corporation
- J.B. Honeycutt, The Use of Aluminum Alkyls in Organic Synthesis (Suppl. 2), Ethyl Corporation, 1979
- (1979) The Use of Aluminum Alkyls in Organic Synthesis , Issue.SUPPL. 2
- Honeycutt, J.B.¹

7
- 0004106458
- Amsterdam: Elsevier
- Mole T. Jeffery E.A. Organoaluminum Compounds 1972 Elsevier Amsterdam
- (1972) Organoaluminum Compounds
- Mole, T.¹ Jeffery, E.A.²

8
- 1842848856
- Ph.D. Dissertation, University of Florida
- V. Abedi, Ph.D. Dissertation, University of Florida, 1991
- (1991)
- Abedi, V.¹

9
- 0002227766
- Niathi J.Z. Ressner J.M. Smith J.D. J. Organomet. Chem. 70 1974 35
- (1974) J. Organomet. Chem. , vol.70 , pp. 35
- Niathi, J.Z.¹ Ressner, J.M.² Smith, J.D.³

10
- 0040648305
- Beachley O.T. Jr. Tessier-Youngs C. Inorg. Chem. 21 1982 1970
- (1982) Inorg. Chem. , vol.21 , pp. 1970
- Beachley Jr., O.T.¹ Tessier-Youngs, C.²

11
- 33845185721
- Saulnier M.G. Kadow J.F. Tun M.M. Vyas D.M. Langley D.R. J. Am. Chem. Soc. 111 1989 8320
- (1989) J. Am. Chem. Soc. , vol.111 , pp. 8320
- Saulnier, M.G.¹ Kadow, J.F.² Tun, M.M.³ Vyas, D.M.⁴ Langley, D.R.⁵

12
- 0005821348
- The cerium (III) reagent of Johnson and Tait may be preferable in the case of readily enolizable aldehydes
- The cerium (III) reagent of Johnson and Tait may be preferable in the case of readily enolizable aldehydes: Johnson R. Tait B.D. J. Org. Chem. 52 1987 281
- (1987) J. Org. Chem. , vol.52 , pp. 281
- Johnson, R.¹ Tait, B.D.²

13
- 1842838109
- - in the reaction mixture appears to assist in breaking up alkylaluminum-oxide aggregates. The latter effect should increase the reactivity of the alane as well as counteract the reduction-oxidation processes which involve an alkoxyaluminum-aldehyde complex (Scheme 1; path b)
- - in the reaction mixture appears to assist in breaking up alkylaluminum-oxide aggregates. The latter effect should increase the reactivity of the alane as well as counteract the reduction-oxidation processes which involve an alkoxyaluminum-aldehyde complex (Scheme 1; path b)

14
- 1842870865
- Scharf H.-D. Kalkoff H. Janus J. Tetrahedron 35 1979 2513
- (1979) Tetrahedron , vol.35 , pp. 2513
- Scharf, H.-D.¹ Kalkoff, H.² Janus, J.³

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