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Volumn 131, Issue 32, 2009, Pages 11280-11281

Stereoselective synthesis of α-alkyl-β-keto imides via asymmetric redox C-C bond formation between α-alkyl-α-diazocarbonyl compounds and aldehydes

Author keywords

[No Author keywords available]

Indexed keywords

C-C BOND FORMATION; CHEMICAL EQUATIONS; GENERAL METHOD; STEREOGENIC CENTERS; STEREOSELECTIVE SYNTHESIS;

EID: 68849108385     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja903500w     Document Type: Article
Times cited : (62)

References (37)
  • 15
    • 0000252759 scopus 로고    scopus 로고
    • Use of arylaldehydes tends to give the aryl transfer products dominantly; see: a
    • Use of arylaldehydes tends to give the aryl transfer products dominantly; see: (a) Mahmood, S. J.; Hossain, M. M. J. Org. Chem. 1998, 63, 3333.
    • (1998) J. Org. Chem , vol.63 , pp. 3333
    • Mahmood, S.J.1    Hossain, M.M.2
  • 24
    • 68849091098 scopus 로고    scopus 로고
    • 1H NMR, which could be separated by column chromatography on silica gel.
    • 1H NMR, which could be separated by column chromatography on silica gel.
  • 25
    • 68849124503 scopus 로고    scopus 로고
    • For the determination of the relative configuration and the discussion on the stereochemical outcome, see Supporting Information
    • For the determination of the relative configuration and the discussion on the stereochemical outcome, see Supporting Information.
  • 26
    • 68849130714 scopus 로고    scopus 로고
    • 2 for 3 days led to the predominant formation of the opposite diastereomer (dr = 1:3).
    • 2 for 3 days led to the predominant formation of the opposite diastereomer (dr = 1:3).
  • 27
    • 38349184575 scopus 로고    scopus 로고
    • For recent examples of Roskamp reaction with α-chiral aldehydes, see: a
    • For recent examples of Roskamp reaction with α-chiral aldehydes, see: (a) Toueg, J.; Prunet, J. Org. Lett. 2008, 10, 45.
    • (2008) Org. Lett , vol.10 , pp. 45
    • Toueg, J.1    Prunet, J.2
  • 32
    • 68849116078 scopus 로고    scopus 로고
    • Zinc borohydride reduction and nucleophilic addition of MeMgI also proceeded with high diasteroselectivity. See Supporting Information
    • Zinc borohydride reduction and nucleophilic addition of MeMgI also proceeded with high diasteroselectivity. See Supporting Information.
  • 37
    • 0033591141 scopus 로고    scopus 로고
    • For the synthetic applications of β-lactones, see
    • For the synthetic applications of β-lactones, see: Yang, H. W.; Romo, D. Tetrahedron 1999, 55, 6403.
    • (1999) Tetrahedron , vol.55 , pp. 6403
    • Yang, H.W.1    Romo, D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.