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Volumn 344, Issue 16, 2009, Pages 2120-2126

Efficient synthesis of d-xylo and d-ribo-phytosphingosines from methyl 2-amino-2-deoxy-β-d-hexopyranosides

Author keywords

Grubbs' catalyst; Olefin cross metathesis; Phytosphingosines; Synthesis

Indexed keywords

EFFICIENT SYNTHESIS; GRUBBS' CATALYST; HIGH YIELD; OLEFIN CROSS-METATHESIS; PHYTOSPHINGOSINES; REDUCTIVE OPENING; SYNTHESIS; SYNTHETIC APPROACH;

EID: 70349758237     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carres.2009.07.007     Document Type: Article
Times cited : (18)

References (54)
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    • Holst, O.1
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    • For recent examples of syntheses of phytosphingosine and derivatives, see: and references cited therein
    • For recent examples of syntheses of phytosphingosine and derivatives, see:. Luo S.-Y., Thorpate S.R., Hsu C.-Y., and Hung S.-C. Tetrahedron Lett. 43 (2002) 4889-4892 and references cited therein
    • (2002) Tetrahedron Lett. , vol.43 , pp. 4889-4892
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    • 70349760367 scopus 로고    scopus 로고
    • For examples of truncated sphingosine and its applications in our group, see: Bundle, D. R, Ling, C.-C, Zhang, P. Patent WO 03/101937; Chem. Abstr. 2003, 140, 16928
    • For examples of truncated sphingosine and its applications in our group, see: Bundle, D. R.; Ling, C.-C.; Zhang, P. Patent WO 03/101937; Chem. Abstr. 2003, 140, 16928.
  • 28
    • 2942752245 scopus 로고    scopus 로고
    • For the syntheses of E-sphingosine via OCM, see:
    • For the syntheses of E-sphingosine via OCM, see:. Torssell S., and Somfai P. Org. Biomol. Chem. 2 (2004) 1643-1646
    • (2004) Org. Biomol. Chem. , vol.2 , pp. 1643-1646
    • Torssell, S.1    Somfai, P.2
  • 34
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    • For the syntheses of phytosphingosine via OCM, see:
    • For the syntheses of phytosphingosine via OCM, see:. Singh O.V., Kampf D.J., and Han H. Tetrahedron Lett. 45 (2004) 7239-7242
    • (2004) Tetrahedron Lett. , vol.45 , pp. 7239-7242
    • Singh, O.V.1    Kampf, D.J.2    Han, H.3
  • 37
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    • Ph.D. Thesis, University of Alberta, September
    • Jacques, S. Ph.D. Thesis, University of Alberta, September, 2008.
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    • Jacques, S.1
  • 53
    • 70349774034 scopus 로고    scopus 로고
    • Compounds 11, 13, 15, and 17 were prepared from truncated 7b. Cai, Y., Ph.D. thesis, University of Alberta, 2008.
    • Compounds 11, 13, 15, and 17 were prepared from truncated 7b. Cai, Y., Ph.D. thesis, University of Alberta, 2008.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.