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Volumn 9, Issue 12, 2011, Pages 4580-4586

Design and synthesis of pyrrolidine-containing sphingomimetics

Author keywords

[No Author keywords available]

Indexed keywords

APOPTOSIS; BIOLOGICAL EVALUATION; CARBON ATOMS; CYCLIC SULFATES; CYTOTOXIC EFFECTS; MIMETICS; NUCLEOPHILIC RING OPENING; PYRROLIDINE MOIETY; PYRROLIDINES; REDUCTIVE CYCLIZATION; REGIO-SELECTIVE; SPHINGOLIPIDS; SYNTHESIS FEATURES;

EID: 79957988189     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c1ob05324h     Document Type: Article
Times cited : (13)

References (65)
  • 32
    • 65949110846 scopus 로고    scopus 로고
    • (2S,3R)-3-Hydroxy-2-(hydroxymethyl)pyrrolidine bearing various C4 lipophilic residues has been synthesized and evaluated. See:
    • J. Cho Y. M. Lee D. Kim S. Kim J. Org. Chem. 2009 74 3900 3904
    • (2009) J. Org. Chem. , vol.74 , pp. 3900-3904
    • Cho, J.1    Lee, Y.M.2    Kim, D.3    Kim, S.4
  • 37
    • 0026516860 scopus 로고
    • According to ref.16, the Staudinger-type reductive cyclization of 1,3-azido nitrile 10 seemed to be feasible to give γ-lactam 14. However, our attempts to effect this reaction were not successful
    • Y. G. Gololobov L. F. Kasukhin Tetrahedron 1992 48 1353 1406
    • (1992) Tetrahedron , vol.48 , pp. 1353-1406
    • Gololobov, Y.G.1    Kasukhin, L.F.2
  • 41
    • 25444457793 scopus 로고    scopus 로고
    • Intermolecular Staudinger ligation of an azide and a carboxylic acid to form an amide group has been reported. See:
    • M. Kawasaki T. Shinada M. Hamada Y. Ohfune Org. Lett. 2005 35 4165 4167
    • (2005) Org. Lett. , vol.35 , pp. 4165-4167
    • Kawasaki, M.1    Shinada, T.2    Hamada, M.3    Ohfune, Y.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.