126753-78-4Relevant articles and documents
Total synthesis of (±)-, (-)-, and (+)-oudemansin X
Umezawa,Nozawa,Nagumo,Akita
, p. 1111 - 1118 (2007/10/02)
Three kinds of oudemansin X, (-)-1, (+)-1 and (±)-1, were totally synthesized. The key point in the present chiral synthesis was the enantioselective acetylation of the racemic alcohols, (±)-5 and (±)-8, using lipase in an organic solvent. The synthetic (-)-1 was found to exhibit strong antifungal activity against several molds and yeasts.
A simple and highly stereoselective route to (→).podocarpic acid
Banerjee,Nasipuri,Pakrashi
, p. 3952 - 3954 (2007/10/02)
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