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Volumn 40, Issue 50, 1999, Pages 8771-8774

A synthesis of L-α-phosphatidyl-D-myo-inositol 4,5-bisphosphate (4,5- PIP2) and glyceryl lipid analogs

Author keywords

Cyclitols; Hydroxylation; Phospholipids; Shikimic acid

Indexed keywords

GLYCEROLIPID; INOSINE DERIVATIVE; PHOSPHATIDYLINOSITOL 4,5 BISPHOSPHATE; SHIKIMIC ACID DERIVATIVE;

EID: 0033544819     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)01877-8     Document Type: Article
Times cited : (16)

References (24)
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    • Ashcroft, F. Science 1998, 282, 1059-1060 and references cited therein.
    • (1998) Science , vol.282 , pp. 1059-1060
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    • 0001260735 scopus 로고
    • Bender, S. L.; Budhu, R. J. J. Am. Chem. Soc. 1991, 113, 9883-9885. Estevez, V. A.; Prestwich, G. D. J. Am. Chem. Soc. 1991, 113, 9885-9887.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 9883-9885
    • Bender, S.L.1    Budhu, R.J.2
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    • 84987580087 scopus 로고
    • Bender, S. L.; Budhu, R. J. J. Am. Chem. Soc. 1991, 113, 9883-9885. Estevez, V. A.; Prestwich, G. D. J. Am. Chem. Soc. 1991, 113, 9885-9887.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 9885-9887
    • Estevez, V.A.1    Prestwich, G.D.2
  • 20
    • 0009475130 scopus 로고    scopus 로고
    • note
    • 31P NMR, IR, and MS analysis using chromatographically homogeneous material.
  • 21
    • 84981773177 scopus 로고
    • Epoxy enol ethers are generally quite labile and are usually only detected as transient species: Effenberger, F. Angew. Chem., Int. Ed. Engl. 1969, 8, 295-400.
    • (1969) Angew. Chem., Int. Ed. Engl. , vol.8 , pp. 295-400
    • Effenberger, F.1
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    • note
    • 4 external reference) δ 0.35, 0.33, -2.10.
  • 24
    • 0009478969 scopus 로고    scopus 로고
    • note
    • 31P NMR analysis, but was typically used in the next step without separation.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.