A facile synthesis of D-ribo-C20-phytosphingosine and its C2 epimer from D-ribose

Carbohydrate Research

Volumn 346, Issue 13, 2011, Pages 1728-1738

  Martinková, Miroslava ^a   Gonda, Jozef ^a   Pomikalová, Kvetoslava ^a   Kožíšek, Jozef ^b   Kuchár, Juraj ^a  

^a P J AFÁRIK UNIVERSITY   (Slovakia)

^b SLOVAK UNIVERSITY OF TECHNOLOGY   (Slovakia)

Author keywords

Overman rearrangement; Phytosphingosine; Sphingolipids; Trichloroacetamides

Indexed keywords

SYNTHESIS (CHEMICAL);

OVERMAN REARRANGEMENT; PHYTOSPHINGOSINES; RIBOSE DERIVATIVES; SPHINGOLIPIDS; SYNTHETIC ROUTES; TRICHLOROACETAMIDES; TRICHLOROACETIMIDATES; WITTIG OLEFINATION;

ORGANIC COMPOUNDS;

2 AMINOICOSANE 1,3,4 TRIOL; 2 AMINOICOSANE 1,3,4 TRIOL (DEXTRO RIBO PHYTOSPHINGOSINE); CARBOHYDRATE DERIVATIVE; DEXTRO RIBO PHYTOSPHINGOSINE; FUNCTIONAL GROUP; JASPINE B; N [[6,7 BIS[(TERT BUTYLDIMETHYLSILYL)OXY] 4,5 (ISOPROPYLIDENEDIOXY)HEPT 1 EN 3 YL]] 2,2,2 TRICHLOROACETAMIDE; N [[6,7 BIS[(TERT BUTYLDIMETHYLSILYL)OXY]4,5 (ISOPROPYLIDENEDIOXY)HEPT 1 EN 3 YL]] 2,2,2 TRICHLOROACETAMIDE; NATURAL PRODUCT; PHYTOSPHINGOSINE; RIBOSE; SPHINGANINE; SPHINGOSINE; TRICHLOROACETIMIDIC ACID; UNCLASSIFIED DRUG;

ARTICLE; CARBOHYDRATE SYNTHESIS; CHEMICAL REACTION; EPIMER; FACILE SYNTHESIS; MOLECULE; OLEFINATION; OVERMAN REARRANGEMENT; PRIORITY JOURNAL; REDUCTION; WITTIG REACTION;

EID: 80053560741     PISSN: 00086215     EISSN: 1873426X     Source Type: Journal    
DOI: 10.1016/j.carres.2011.05.028     Document Type: Article

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