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Volumn 130, Issue 10, 2008, Pages 2916-2917

Rh-catalyzed carbonyl hydroacylation: an enantioselective approach to lactones

Author keywords

[No Author keywords available]

Indexed keywords

CARBONYL DERIVATIVE; LACTONE; RHODIUM;

EID: 41449097197     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja7109025     Document Type: Article
Times cited : (110)

References (20)
  • 1
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    • For reviews, see: a
    • For reviews, see: (a) Cane, D. E. Chem. Rev. 1997, 97, 2463.
    • (1997) Chem. Rev , vol.97 , pp. 2463
    • Cane, D.E.1
  • 4
    • 84890779821 scopus 로고    scopus 로고
    • For a review, see:, Evans, P. A, Ed, Wiley-VCH: New York, and references therein
    • For a review, see: Fu, G. C. In Modern Rhodium-Catalyzed Reactions; Evans, P. A., Ed.; Wiley-VCH: New York, 2005; pp 79-91 and references therein.
    • (2005) Modern Rhodium-Catalyzed Reactions , pp. 79-91
    • Fu, G.C.1
  • 5
    • 22544471229 scopus 로고    scopus 로고
    • To our knowledge, there are no other transition metal-catalyzed ketone hydroacylations. For Rh- and Ru-catalyzed aldehyde hydroacylation, see: a
    • To our knowledge, there are no other transition metal-catalyzed ketone hydroacylations. For Rh- and Ru-catalyzed aldehyde hydroacylation, see: (a) Fuji, K.; Morimoto, T.; Tsutsumi K.; Kakiuchi, K. Chem. Commun. 2005, 3295.
    • (2005) Chem. Commun , pp. 3295
    • Fuji, K.1    Morimoto, T.2    Tsutsumi, K.3    Kakiuchi, K.4
  • 11
    • 0141920762 scopus 로고    scopus 로고
    • For a Tishchenko review, see
    • (a) For a Tishchenko review, see: Mahrwald, R. Curr. Org. Chem. 2003, 7, 1713.
    • (2003) Curr. Org. Chem , vol.7 , pp. 1713
    • Mahrwald, R.1
  • 12
    • 0035861769 scopus 로고    scopus 로고
    • For an asymmetric Tishchenko, see
    • (b) For an asymmetric Tishchenko, see: Hsu, J. L.; Fang, J. M. J. Org. Chem. 2001, 66, 8573.
    • (2001) J. Org. Chem , vol.66 , pp. 8573
    • Hsu, J.L.1    Fang, J.M.2
  • 13
    • 0001321315 scopus 로고
    • For reviews on the benzoin reaction, see: a
    • For reviews on the benzoin reaction, see: (a) Ide, W. S.; Buck, J. S. Org. React. 1948, 4, 269.
    • (1948) Org. React , vol.4 , pp. 269
    • Ide, W.S.1    Buck, J.S.2
  • 16
  • 18
    • 41449091301 scopus 로고    scopus 로고
    • Chelation has been proposed to stabilize Rh(III)-acyl intermediates and suppress decarbonylation; see: (a) ref 5a.
    • Chelation has been proposed to stabilize Rh(III)-acyl intermediates and suppress decarbonylation; see: (a) ref 5a.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.