Direct conversion of benzyl alcohol to ketone by polymer-supported Rh catalyst

Tetrahedron Letters

Volumn 40, Issue 50, 1999, Pages 8897-8900

  Jun, Chul Ho ^a   Hong, Hye Suk ^a   Huh, Chan Woo ^a  

^a Yonsei University   (South Korea)

Author keywords

Catalysis; Ketones; Rhodium; Rhodium compounds; Supported reagents reactions

Indexed keywords

BENZYL ALCOHOL; KETONE; POLYMER; POLYSTYRENE; RHODIUM COMPLEX;

ARTICLE; CATALYSIS; CATALYST; CHEMICAL REACTION; COMPLEX FORMATION; POLYMERIZATION; REACTION ANALYSIS;

EID: 0033544778     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)01907-3     Document Type: Article

References (14)

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7. For review, see: Cornils, B.; Herrmann, W. A. In Applied Homogeneous Catalysis with Organometallic Compounds; Cornils, B.; Herrmann, W. A., Eds.; VCH: New York, 1996; Vol. 2, pp. 575-601.
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11. (c) Frechet, J. M. Tetrahedron 1981, 37, 663-683.
12. 3 on decanting and washing at the first run) and 303 mg 2a were added. The reaction was carried out under the previous reaction conditions to give 49.2 mg 6a (72%).
13. When the reaction was carried out with benzaldehyde instead of 1a, no reaction occurred.
14. Osborn, J. A.; Wilkinson, G. In Reagents for Transition Metal Complex and Organometallic Syntheses; Angelici, R., Ed.; Wiley: New York, 1989; Vol. 28, pp. 77-79.