Asymmetric epoxidation of allylic alcohols employing 4,5-diphenyloxazole as a masked ester functionality
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Enantiospecific syntheses of leukotrienes C4, D4, and E4, and [14,15-3H2]leukotriene E4 dimethyl ester
2. Asymmetric epoxidation provides shortest routes to four chiral epoxy alcohols which are key intermediates in syntheses of methymycin, erythromycin, leukotriene C-1, and disparlure
3. Chirally directed synthesis of (-)-methyl 5(S), 6(S)-oxido-7-hydroxyheptanoate, a key intermediate for the total synthesis of leukotrienes A, C, D and E
4. Tetrahedron;Wasserman,1981
5. Oxazoles as masked activated carboxylates. Synthesis of (±)-di-O-methylcurvularin
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