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Volumn 212, Issue 1, 1997, Pages 203-204

Crystal structure of (2R,3S,4S)-N,3-O-dibenzyl-2-butyl-3,4-dihydroxy-pyrrolidine, C22H29NO2

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Indexed keywords


EID: 0345125419     PISSN: 14337266     EISSN: None     Source Type: Journal    
DOI: 10.1524/ncrs.1997.212.1.203     Document Type: Article
Times cited : (1)

References (6)
  • 1
    • 85025242443 scopus 로고    scopus 로고
    • Concise synthesis of deacetylanisomycin and 2-substituted analogues from N,2-O-dibenzyl-L-threose imine.
    • In print.
    • Veith, U.; Schwardt, O.; Jäger, V.: Concise synthesis of deacetylanisomycin and 2-substituted analogues from N,2-O-dibenzyl-L-threose imine. Synlett. In print.
    • Synlett.
    • Veith, U.1    Schwardt, O.2    Jäger, V.3
  • 3
    • 1842584396 scopus 로고    scopus 로고
    • Auxiliary-controlled diastereoselection by N-(1-phenylethy 1) in Grignard additions to 2-O-benzyl-glyceraldehyde imines.
    • Veith, U.; Leurs, S.; Jäger, V.: Auxiliary-controlled diastereoselection by N-(1-phenylethy 1) in Grignard additions to 2-O-benzyl-glyceraldehyde imines. J. Chem. Soc. Chem. Commun. (1996) 329-330.
    • (1996) J. Chem. Soc. Chem. Commun. , pp. 329-330
    • Veith, U.1    Leurs, S.2    Jäger, V.3
  • 4
    • 0027162483 scopus 로고
    • Anisomycin and new congeners active against human tumor cell lines.
    • Hosoya, Y.; Kameyama, T.; Naganawa, H.; Okami, Y.; Takeuchi, T.: Anisomycin and new congeners active against human tumor cell lines. J. AntibioL 46 (1993) 1300-1302.
    • (1993) J. AntibioL , vol.46 , pp. 1300-1302
    • Hosoya, Y.1    Kameyama, T.2    Naganawa, H.3    Okami, Y.4    Takeuchi, T.5
  • 6
    • 85025284865 scopus 로고
    • SHELXL-93, a program for refining crystal structures.
    • Germany
    • Sheldrick, G. M.: SHELXL-93, a program for refining crystal structures. University of Göttingen, Germany 1993.
    • (1993) University of Göttingen
    • Sheldrick, G.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.