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Volumn 132, Issue 43, 2010, Pages 15182-15184

Enantioselective synthesis of syn - And anti -1,3-aminoalcohols via β-aminoketones and subsequent reduction/dynamic kinetic asymmetric transformation

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ALCOHOLS; ASYMMETRIC TRANSFORMATIONS; DIASTEREOMERS; ENANTIO; ENANTIOSELECTIVE SYNTHESIS; HIGH YIELD; MANNICH REACTIONS; ORGANOCATALYTIC; STEREOGENIC CENTERS;

EID: 78049380161     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja107857v     Document Type: Article
Times cited : (63)

References (30)
  • 21
    • 78049354959 scopus 로고    scopus 로고
    • See the Supporting Information
    • See the Supporting Information.
  • 29
    • 78049393470 scopus 로고    scopus 로고
    • 2 atmosphere, the (2 R,4 S)- 2a /(2 S,4 R)- 4a /(S)- 1a ratio was 70:30:0, and (2 R,4 S)- 4a could not be detected
    • 2 atmosphere, the (2 R,4 S)- 2a /(2 S,4 R)- 4a /(S)- 1a ratio was 70:30:0, and (2 R,4 S)- 4a could not be detected.
  • 30
    • 78049363979 scopus 로고    scopus 로고
    • The ee of 2f could not be determined with precision because of peak overlap in the HPLC analysis, as the peak of the minor enantiomer overlapped with the peak of the minor diastereoisomer. Since the major part of the small peak was attributed to the minor diastereoisomer, we indirectly concluded that the ee was >99%
    • The ee of 2f could not be determined with precision because of peak overlap in the HPLC analysis, as the peak of the minor enantiomer overlapped with the peak of the minor diastereoisomer. Since the major part of the small peak was attributed to the minor diastereoisomer, we indirectly concluded that the ee was >99%.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.