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Volumn 40, Issue 8, 2010, Pages 1099-1105

Improved enantioselective synthesis of protected (3S,4S)-4-amino-3,5- dihydroxypentanoic acid (ADPA)

Author keywords

amino b hydroxy acids; ADPA; Enantioselective synthesis

Indexed keywords

4 AMINO 3,5 DIHYDROXYPENTANOIC ACID; BETA KETO ESTER; ESTER; MAGNESIUM SALT; METHYL ESTER; SERINE; TERT BUTYL ESTER; UNCLASSIFIED DRUG; VALERIC ACID;

EID: 77949369934     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910903029958     Document Type: Article
Times cited : (1)

References (9)
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  • 4
    • 0001638532 scopus 로고    scopus 로고
    • An improved enantiospecific synthesis of statine and statine analogs via 4-(N,N-dibenzylamino)-3-keto esters
    • Hoffman, R. V.; Tao, J. An improved enantiospecific synthesis of statine and statine analogs via 4-(N,N-dibenzylamino)-3-keto esters. J. Org. Chem. 1997, 62, 2292-2297.
    • (1997) J. Org. Chem. , vol.62 , pp. 2292-2297
    • Hoffman, R.V.1    Tao, J.2
  • 5
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    • Approaches to the synthesis of (2R,3S)-2-hydroxymethylpyr-rolidin-3-ol (CYB-3) and its C(3) epimer: A cautionary tale
    • Hulme, A. N.; Curley, K. S. Approaches to the synthesis of (2R,3S)-2-hydroxymethylpyr-rolidin-3-ol (CYB-3) and its C(3) epimer: A cautionary tale. J. Chem. Soc, Perkin Trans. 1 2002, 1, 1083-1091.
    • (2002) J. Chem. Soc, Perkin Trans. 1 , vol.1 , pp. 1083-1091
    • Hulme, A.N.1    Curley, K.S.2
  • 7
    • 0035478942 scopus 로고    scopus 로고
    • Diastereoselective synthesis of enantiopure y-amino-P-hydroxy acids by Reformatsky reaction of chiral a-dibenzylamino aldehydes
    • D \ \3.8 (c= 1.0, CDCl3). See
    • D \ \3.8 (c= 1.0, CDCl3). See Andres, J. M.; Pedrosa, R.; Perez, A.; Perez-Encabo, A. Diastereoselective synthesis of enantiopure y-amino-P-hydroxy acids by Reformatsky reaction of chiral a-dibenzylamino aldehydes. Tetrahedron 2001, 57, 8521-8530.
    • (2001) Tetrahedron , vol.57 , pp. 8521-8530
    • Andres, J.M.1    Pedrosa, R.2    Perez, A.3    Perez-Encabo, A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.