CHIRAL PROPIONATE ENOLATE EQUIVALENTS FOR THE STEREOSELECTIVE SYNTHESIS OF THREO-ALPHA-METHYL-BETA-HYDROXY OR ERYTHRO-ALPHA-METHYL-BETA-HYDROXY ACIDS

CHIRAL PROPIONATE ENOLATE EQUIVALENTS FOR THE STEREOSELECTIVE SYNTHESIS OF THREO-ALPHA-METHYL-BETA-HYDROXY OR ERYTHRO-ALPHA-METHYL-BETA-HYDROXY ACIDS

Manylion Llyfryddiaeth
Prif Awduron:	Davies, S, Dordorhedgecock, I, Warner, P
Fformat:	Journal article
Cyhoeddwyd:	1985

Eitemau Tebyg

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Specific tritium labeling of cerebrosides at the 3-positions of erythro-sphingosine and threo-sphingosine
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The direct catalytic enantioselective synthesis of protected aryl beta-hydroxy-alpha-amino acids.
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threo-Diethyl 2-ethyl-2-hydroxy-3-(4-methylbenzenesulfonamido)succinate
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Synthesis of new bile acid analogues and their metabolism in the hamster: 3 alpha, 6 alpha-dihydroxy-6 beta-methyl-5 beta-cholanoic acid and 3 alpha, 6 beta-dihydroxy-6 alpha-methyl-5 beta-cholanoic acid.
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Sterol synthesis : chemical synthesis of 3 beta-hydroxy-5 alpha-cholest-7-ene-9 alpha-carbonitrile.
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Occurrence of 3 beta-hydroxy-5-cholestenoic acid, 3 beta,7 alpha-dihydroxy-5-cholestenoic acid, and 7 alpha-hydroxy-3-oxo-4-cholestenoic acid as normal constituents in human blood.
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