Trifluoromethyl derivatization of the ganglioside, GM1

Synthesis

Volumn , Issue 11, 2010, Pages 1905-1908

  Liu, Zhao ^a   Kumar, Krishna ^a,b  

^a TUFTS UNIVERSITY   (United States)

^b TUFTS MEDICAL CENTER   (United States)

Author keywords

Fluorine; Glycolipids; Natural products; Sphingolipids

Indexed keywords

ACYL CHAIN; BOVINE BRAIN; CHEMICAL BIOLOGY; CHEMICAL MANIPULATION; CHEMICAL TRANSFORMATIONS; DERIVATIZATION OF; GLYCOLIPIDS; GLYCOSPHINGOLIPIDS; MASS SPECTRAL; NATURAL PRODUCTS; NATURALLY OCCURRING; REGIO-SELECTIVE; SOFT TISSUE; SPHINGOLIPIDS; SYNTHETIC ROUTES; TRIFLUOROMETHYL;

BIOLOGY; ESTERS; FLUORINE;

LIPIDS;

15 OXOPENTADECANOATE; 18,18,18 TRIFLUOROOCTADEC 15 ENOATE; 18,18,18 TRIFLUOROSTEARIC ACID; DEACETYL LYSO GANGLIOSIDE GM1; GANGLIOSIDE GM1; GLYCOSPHINGOLIPID; LYSO GANGLIOSIDE GM1; METHYL 15 HYDROXYPENTADECANOATE; METHYL 15 OXOPENTADECANOATE; METHYL 18,18,18 TRIFLUOROOCTADEC 15 ENOATE; METHYL 18,18,18 TRIFLUOROOCTADECANOATE; N FMOC LYSO GANGLIOSIDE GM1; N SUCCINIMIDYL 18,18,18 TRIFLUOROSTEARATE; PHOSPHONIUM DERIVATIVE; TRIFLUORO GANGLIOSIDE GM1; TRIFLUOROSTEARIC ACID; TRIPHENYL(3,3,3 TRIFLUOROPROPYL)PHOSPHONIUM IODIDE; UNCLASSIFIED DRUG;

ARTICLE; BIOPHYSICS; CHEMICAL STRUCTURE; CYTOLOGY; MASS SPECTROMETRY; MOLECULAR BIOLOGY; NONHUMAN; SOFT TISSUE; SYNTHESIS;

EID: 77952762714     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0029-1218777     Document Type: Article

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