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Volumn 12, Issue 12, 2010, Pages 2762-2765

Enantioselective synthesis of syn / anti -1,3-amino alcohols via proline-catalyzed sequential α-aminoxylation/α-amination and horner-wadsworth-emmons olefination of aldehydes

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; ALKENE; AMINOALCOHOL; PROLINE;

EID: 77953589791     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol100856u     Document Type: Article
Times cited : (54)

References (60)
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    • For excellent reviews on the use of chiral 1,3-amino alcohol in asymmetric organic synthesis see
    • For excellent reviews on the use of chiral 1,3-amino alcohol in asymmetric organic synthesis see: Lait, S. M.; Rankic, D. A.; Keay, B. A. Chem. Rev. 2007, 107, 767
    • (2007) Chem. Rev. , vol.107 , pp. 767
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  • 18
    • 77953546922 scopus 로고    scopus 로고
    • Asymmetric synthesis of 1,3-amino alcohols
    • Asymmetric synthesis of 1,3-amino alcohols
  • 22
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    • For a review see: Tramontini, M. Synthesis 1982, 605
    • (1982) Synthesis , vol.605
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    • For reduction of enantiopure β-amino ketones see
    • For reduction of enantiopure β-amino ketones see: Davis, F. A.; Prasad, K. R.; Nolt, B. M.; Wu, Y. Org. Lett. 2003, 5, 923
    • (2003) Org. Lett. , vol.5 , pp. 923
    • Davis, F.A.1    Prasad, K.R.2    Nolt, B.M.3    Wu, Y.4
  • 34
    • 0037043180 scopus 로고    scopus 로고
    • For a review of proline-catalyzed asymmetric reactions, see
    • For a review of proline-catalyzed asymmetric reactions, see: List, B. Tetrahedron 2002, 58, 5573.
    • (2002) Tetrahedron , vol.58 , pp. 5573
    • List, B.1
  • 39
    • 4344651796 scopus 로고    scopus 로고
    • For a comprehensive review on α-aminoxylation, see, and references cited therein
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    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 2995
    • Merino, P.1    Tejero, T.2
  • 41
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    • For reviews on organocatalytic tandem reactions, see
    • For reviews on organocatalytic tandem reactions, see: Notz, W.; Tanaka, F.; Barbas, C. F., III. Acc. Chem. Res. 2004, 37, 580
    • (2004) Acc. Chem. Res. , vol.37 , pp. 580
    • Notz, W.1    Tanaka, F.2    Barbas Iii, C.F.3
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    • note
    • The relative stereochemistry of amino alcohols 4 and 5 was determined by NMR and also on the basis of NOESY studies of the cyclic carbamates 14 and 17 derived from anti-4a and syn-5a, respectively (see Supporting Information).
  • 57
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    • For a review on 1,2-amino alcohols see
    • For a review on 1,2-amino alcohols see


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.