A common and stereoselective strategy for the synthesis of N,O,O,O-tetra-acetyl d-ribo-(2S,3S,4R)-phytosphingosine and 2-epi-jaspine B

Authors :: Srinivas Rao, G.
Venkateswara Rao, B.
Source :: Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry. Sep2011, Vol. 52 Issue 38, p4861-4864. 4p.
Publication Year :: 2011
Abstract: Abstract: A common and stereoselective strategy for the synthesis of N,O,O,O-tetra-acetyl d-ribo-(2S,3S,4R)-phytosphingosine and 2-epi-jaspine B was achieved by using Grignard addition on N-benzyl sugar lactamine and Wittig olefination as key steps. [Copyright &y& Elsevier]

Subjects :: *ORGANIC synthesis
*STEREOCHEMISTRY
*SPHINGOSINE
*GRIGNARD reagents
*ADDITION reactions
*AMINES
*WITTIG reaction
*ALKENES

Language :: English
ISSN :: 00404039
Volume :: 52
Issue :: 38
Database :: Academic Search Index
Journal :: Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry
Publication Type :: Academic Journal
Accession number :: 64481935
Full Text :: https://doi.org/10.1016/j.tetlet.2011.07.032

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