Oxazine formation by MsCl/Et 3N as a convenient tool for the stereochemical interconversion of the hydroxyl group in N-acetyl 1,3-aminoalcohols. Asymmetric synthesis of N-acetyl L-xylo- and L-arabino-phytosphingosines

Tetrahedron Letters

Volumn 45, Issue 39, 2004, Pages 7239-7242

  Singh, Om V ^a   Kampf, Dorothy J ^a   Han, Hyunsoo ^a  

^a UNIVERSITY OF TEXAS AT SAN ANTONIO   (United States)

Author keywords

Olefin cross metathesis; Oxazine; Phytosphingosine; Regioselective asymmetric aminohydroxylation

Indexed keywords

AMINOALCOHOL; HYDROXYL GROUP; N ACETYLARABINOPHYTOSPHINGOSINE; N ACETYLPHYTOSPHINGOSINE; PHYTOSPHINGOSINE; UNCLASSIFIED DRUG;

ARTICLE; ASYMMETRIC SYNTHESIS; GRIGNARD REACTION; HYDROLYSIS; MITSUNOBU REACTION; RING CLOSING METATHESIS; STEREOCHEMISTRY; SYNTHESIS;

EID: 4444380439     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.08.030     Document Type: Article

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