aigialomycin-d has been researched along with monorden* in 1 studies
1 other study(ies) available for aigialomycin-d and monorden
Article | Year |
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Total synthesis of aigialomycin D.
[reaction: see text] The first total synthesis of resorcinylic macrolide aigialomycin D was described. The resorcinylic moiety was constructed by a highly efficient Diels-Alder reaction using a disiloxydiene and a 14-membered "ynolide" as the dienophile synthesized by ring-forming olefin metathesis. Topics: Cyclopropanes; Lactones; Macrolides; Molecular Structure; Stereoisomerism | 2004 |