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Volumn 7, Issue 9, 1996, Pages 2585-2593

Synthesis of enantiomerically pure (2R,5S)- and (2R,5R)-5-hydroxypipecolic acid from glycinate Schiff bases

Author keywords

[No Author keywords available]

Indexed keywords

PIPECOLIC ACID DERIVATIVE;

EID: 0030250010     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/0957-4166(96)00332-1     Document Type: Article
Times cited : (40)

References (27)
  • 1
    • 85030275873 scopus 로고    scopus 로고
    • The configuration of the 5-hydroxypipecolic acid derivatives is indicated in one of the following ways: position 5: cis-and irons-hydroxy or 5R and 5S, respectively; position 2 : D and L-aminoacid or 2R and 2S, respectively
    • 1. The configuration of the 5-hydroxypipecolic acid derivatives is indicated in one of the following ways: position 5: cis-and irons-hydroxy or 5R and 5S, respectively; position 2 : D and L-aminoacid or 2R and 2S, respectively.
  • 5
    • 0011883252 scopus 로고
    • Eds. L. Reinhold and Y. Liwischitz, Wiley London
    • (d) Fowden L., Progress in Phytochemistry, Eds. L. Reinhold and Y. Liwischitz, Wiley London, 1970, 2, 203.
    • (1970) Progress in Phytochemistry , vol.2 , pp. 203
    • Fowden, L.1
  • 21
    • 85030278651 scopus 로고    scopus 로고
    • 3OH, which was possible only with pyrrolidine structure); 190; 170; 146
    • 3OH, which was possible only with pyrrolidine structure); 190; 170; 146.
  • 23
    • 85030268870 scopus 로고    scopus 로고
    • 2Ph), 7.26 (5H, s, Ph)
    • 2Ph), 7.26 (5H, s, Ph).
  • 25
    • 84981003593 scopus 로고
    • 12. 2-hydroxypinan-3-one was prepared by the method of H. Schmidt, Chem. Ber. 1960, 93, 2485.
    • (1960) Chem. Ber. , vol.93 , pp. 2485
    • Schmidt, H.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.