SCOPUS 정보 검색 플랫폼

Volumn 39, Issue 29, 1998, Pages 5237-5238

A mild aldol reaction of aryl aldehydes through palladium-catalyzed hydrosilation of α,β-unsaturated carbonyl compounds with trichlorosilane

Author keywords

[No Author keywords available]

Indexed keywords

CARBONYL DERIVATIVE; PALLADIUM;

ARTICLE; CATALYSIS; METAL BINDING; OXIDATION REDUCTION REACTION; REACTION ANALYSIS; STEREOCHEMISTRY; SYNTHESIS;

EID: 0032537679 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(98)01030-2 Document Type: Article

Times cited : (67)

References (11)

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- 1. Rhodium-catalyzed hydrosilation of α,β-unsaturated carbonyl compounds to give silyl ketene acetals and silyl enol ethers: (a) Ojima, I.; Kogure, T.; Nagai, Y. Tetrahedron Lett. 1972, 5035-5038.
- (1972) Tetrahedron Lett. , pp. 5035-5038
- Ojima, I.¹ Kogure, T.² Nagai, Y.³

2
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- (b) Revis, A.; Hilty, T. K. J. Org. Chem. 1990, 55, 2972-2973.
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- Revis, A.¹ Hilty, T.K.²

3
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- 2. Isayama, S.; Mukaiyama, T. Chem. Lett. 1989, 2005-2008.
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4
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- 3. Matsuda, I.; Takahashi, K.; Sato, S. Tetrahedron Lett. 1990, 31, 5331-5334.
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- Matsuda, I.¹ Takahashi, K.² Sato, S.³

5
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- 4. (a) Sato, S.; Matsuda, I.; Izumi, Y. Tetrahedron Lett. 1986, 27, 5517-5520.
- (1986) Tetrahedron Lett. , vol.27 , pp. 5517-5520
- Sato, S.¹ Matsuda, I.² Izumi, Y.³

6
- 0000556498
- (b) Slough, G. A. ; Bergman, R. G.; Heathcock, C. H. J. Am. Chem. Soc. 1989, 111, 938-949.
- (1989) J. Am. Chem. Soc. , vol.111 , pp. 938-949
- Slough, G.A.¹ Bergman, R.G.² Heathcock, C.H.³

7
- 0347195435
- 13C chemical shifts of carbinol carbon in comparison with the reported data ( (a) Heathcock, C. H.; Buse C. T.; Kleschick, W. A.; Pirrung M. C.; Sohn, J. E., Lampe, J. J. Org. Chem. 1980, 45, 1066-1081.
- (1980) J. Org. Chem. , vol.45 , pp. 1066-1081
- Heathcock, C.H.¹ Buse, C.T.² Kleschick, W.A.³ Pirrung, M.C.⁴ Sohn, J.E.⁵ Lampe, J.⁶

8
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- (b) Heathcock, C. H.; Pirrung, M. C. ; Sohn, J. E. Ibid. 1979, 44, 4294-4299.
- (1979) J. Org. Chem. , vol.44 , pp. 4294-4299
- Heathcock, C.H.¹ Pirrung, M.C.² Sohn, J.E.³

9
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- (c) Mulzer, J.; Zippel, M.; Brüntrup, G.; Segner, J.; Finke, J. LiebigsAnn. Chem. 1980, 1108-1134.), as listed below: syn-3a. (2.7 Hz, 73.1ppm), anti-3a (5.8 Hz, 76.3 ppm); syn-3b (2.0 Hz, 69.5 ppm), anti-3b (5.1 Hz, 73.3 ppm); syn-3c (2.2 Hz, 73.0 ppm), anti-3c (5.8 Hz, 76.5 ppm); syn-3d (2.0 Hz, 73.2 ppm), anti-3d (6.1 Hz, 76.6 ppm); syn-3e (2.0 Hz, 72.5 ppm), anti-3e (6.8 Hz, 75.7 ppm);syn-3f (1.7 Hz, 72.6 ppm), anti-3f (7.1 Hz, 75.9 ppm); syn-3g (4.12 Hz, 73.8 ppm), anti-3g (7.6 Hz, 76.3 ppm); syn-3h (4.12 Hz, 73.7 ppm), anti-3h (8.0 Hz, 76.5 ppm); syn-3i (4.12 Hz, 73.6 ppm), anti-3i (7.8 Hz, 76.1 ppm).
- (1980) Liebigsann. Chem. , pp. 1108-1134
- Mulzer, J.¹ Zippel, M.² Brüntrup, G.³ Segner, J.⁴ Finke, J.⁵

10
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- 6. Denmark, S. E.; Winter, S. B. D.; Su, X.; Wong, K. -T. J. Am. Chem. Soc. 1996, 118, 7404-74
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11
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- (b)Denmark, S. E.; Wong, K. -T.; Stavenger, R. A. Ibid. 1997, 119, 2333-2334.
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- Denmark, S.E.¹ Wong, K.-T.² Stavenger, R.A.³

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