A stereocontrolled route to d-ribo-phytosphingosine and sphinganine from an achiral secondary homoallylic alcohol using Sharpless kinetic resolution

Tetrahedron

Volumn 69, Issue 19, 2013, Pages 3817-3822

  Devi, Thongam Joymati ^a   Saikia, Bishwajit ^a   Barua, Nabin C ^a  

^a NATIONAL CHEMICAL LABORATORY   (India)

Author keywords

Sphingolipid Phytosphingosine Sphinganine Apoptosis Regioselective

Indexed keywords

CARBOXYLIC ACID; CINNAMALDEHYDE; DEXTRO RIBO PHYTOSPHINGOSINE; EPOXIDE; PHYTOSPHINGOSINE; SPHINGANINE; UNCLASSIFIED DRUG;

ALLYLATION; ARTICLE; CHIRALITY; COLUMN CHROMATOGRAPHY; ENANTIOSELECTIVITY; PRIORITY JOURNAL; ROOM TEMPERATURE; SHARPLESS EPOXIDATION; STEREOISOMERISM; SYNTHESIS; WITTIG REACTION;

EID: 84875964924     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2013.03.057     Document Type: Article

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