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Volumn 65, Issue 29-30, 2009, Pages 5849-5854

A practical synthesis of optically active arylglycines via catalytic asymmetric Strecker reaction

Author keywords

Asymmetric; Catalyst; Hydrocyanation; Imine

Indexed keywords

GLYCINE DERIVATIVE; N TERT BUTYLOXYCARBONYL 1 NAPHTHYLGLYCINE METHYL ESTER; N TERT BUTYLOXYCARBONYL 2 BROMOPHENYLGLYCINE METHYL ESTER; N TERT BUTYLOXYCARBONYL 2 CHLOROPHENYLGLYCINE METHYL ESTER; N TERT BUTYLOXYCARBONYL 2 METHYLPHENYLGLYCINE METHYL ESTER; N TERT BUTYLOXYCARBONYL 3 FLUOROPHENYLGLYCINE METHYL ESTER; N TERT BUTYLOXYCARBONYL 4 BROMOPHENYLGLYCINE METHYL ESTER; N TERT BUTYLOXYCARBONYL 4 CHLOROPHENYLGLYCINE METHYL ESTER; N TERT BUTYLOXYCARBONYL 4 METHYLPHENYLGLYCINE METHYL ESTER; N TERT BUTYLOXYCARBONYL PHENYLGLYCINE METHYL ESTER; UNCLASSIFIED DRUG;

EID: 67149115145     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.04.098     Document Type: Article
Times cited : (23)

References (56)
  • 19
    • 67149098388 scopus 로고    scopus 로고
    • Reviews
    • Reviews:
  • 21
  • 24
    • 67149140015 scopus 로고    scopus 로고
    • Recent examples of metal catalysts
    • Recent examples of metal catalysts:
  • 28
    • 67149108769 scopus 로고    scopus 로고
    • Recent examples of organocatalysts
    • Recent examples of organocatalysts:
  • 35
    • 67149136897 scopus 로고    scopus 로고
    • Chiral phase transfer catalyzed variants of asymmetric Strecker reactions have recently been reported
    • Chiral phase transfer catalyzed variants of asymmetric Strecker reactions have recently been reported:
  • 39
    • 67149087417 scopus 로고    scopus 로고
    • However, none of the examples includes α-aryl substrates presumably due to their ease of racemization under basic conditions required for the PTC reactions. See also:
    • However, none of the examples includes α-aryl substrates presumably due to their ease of racemization under basic conditions required for the PTC reactions. See also:


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.