xestoaminol-c and safingol

xestoaminol-c has been researched along with safingol* in 1 studies

Other Studies

1 other study(ies) available for xestoaminol-c and safingol

Article	Year
Asymmetric synthesis of vicinal amino alcohols: xestoaminol C, sphinganine and sphingosine. Organic & biomolecular chemistry, 2008, May-07, Volume: 6, Issue:9 The highly diastereoselective anti-aminohydroxylation of alpha,beta-unsaturated esters, via conjugate addition of lithium (S)-N-benzyl-N-(alpha-methylbenzyl)amide and subsequent in situ enolate oxidation with (+)-(camphorsulfonyl)oxaziridine, has been used as the key step in the asymmetric synthesis of N,O-diacetyl xestoaminol C (41% yield over 8 steps), N,O,O-triacetyl sphinganine (30% yield over 8 steps) and N,O,O-triacetyl sphingosine (30% yield over 7 steps). Topics: Fatty Alcohols; Molecular Conformation; Sphingosine; Stereoisomerism	2008

Article

Year

Asymmetric synthesis of vicinal amino alcohols: xestoaminol C, sphinganine and sphingosine.

Organic & biomolecular chemistry, 2008, May-07, Volume: 6, Issue:9

The highly diastereoselective anti-aminohydroxylation of alpha,beta-unsaturated esters, via conjugate addition of lithium (S)-N-benzyl-N-(alpha-methylbenzyl)amide and subsequent in situ enolate oxidation with (+)-(camphorsulfonyl)oxaziridine, has been used as the key step in the asymmetric synthesis of N,O-diacetyl xestoaminol C (41% yield over 8 steps), N,O,O-triacetyl sphinganine (30% yield over 8 steps) and N,O,O-triacetyl sphingosine (30% yield over 7 steps).

Topics: Fatty Alcohols; Molecular Conformation; Sphingosine; Stereoisomerism

2008