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Volumn , Issue 5, 2010, Pages 757-762

Enantioselective synthesis of homosphingosine derivatives from L-aspartic acid

Author keywords

Ceramide; Diastereoselectivity; Enantioselectivity; Sphingosine

Indexed keywords

CERAMIDES; DIASTEREO-SELECTIVITY; ENANTIOPURE; ENANTIOSELECTIVE SYNTHESIS; ERYTHRO; L-ASPARTIC ACID; PROTECTING GROUP; SPHINGOSINE; STERICALLY DEMANDING; WADSWORTH-EMMONS OLEFINATION;

EID: 77955361407     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/S-0029-1219081     Document Type: Article
Times cited : (8)

References (29)
  • 1
  • 21
    • 4344674379 scopus 로고    scopus 로고
    • Compound 10 has been reported in the literature, however, without data, see
    • Compound 10 has been reported in the literature, however, without data, see: Kaul, R.; Brouillette, Y.; Sajjadi, Z.; Hansford, K. A.; Lubell, W. D. J. Org. Chem. 2004, 69, 6131.
    • (2004) J. Org. Chem. , vol.69 , pp. 6131
    • Kaul, R.1    Brouillette, Y.2    Sajjadi, Z.3    Hansford, K.A.4    Lubell, W.D.5
  • 22
    • 77955364393 scopus 로고    scopus 로고
    • 1 (No. 19); a = 14.9329 (6) Å, b = 15.1590 (5) Å, c = 17.2261 (5) Å; R1 = 0.0573, wR2 = 0.0936 (I > 2σ). CCDC 255363-255365 contain the supplementary crystallographic data (excluding structure factors) for this paper. These data can be obtained online free of charge or from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB21EZ UK [fax: (+44)1223336033; or deposit@ccdc.cam.ac.uk]
    • 1 (No. 19); a = 14.9329 (6) Å, b = 15.1590 (5) Å, c = 17.2261 (5) Å; R1 = 0.0573, wR2 = 0.0936 (I > 2σ). CCDC 255363-255365 contain the supplementary crystallographic data (excluding structure factors) for this paper. These data can be obtained online free of charge or from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB21EZ UK [fax: (+44)1223336033; or deposit@ccdc.cam.ac.uk].
  • 29
    • 77955403008 scopus 로고    scopus 로고
    • The stereochemistry was assigned based on analogy with previous reductions, as well as on the coupling constants for similar compounds; see, for example, ref. 8d
    • The stereochemistry was assigned based on analogy with previous reductions, as well as on the coupling constants for similar compounds; see, for example, ref. 8d.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.