Organic Letters · 2006 · 52 citations · 31 references
An asymmetric synthesis of the marine metabolite bistramide A is reported. The synthesis relies on the utility of three different organosilane reagents to construct all principle fragments and 8 of the 11 stereogenic centers of the natural product. [structure: see text].
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Recent advances in the staudinger reaction
Yuri G. Gololobov, L. F. Kasukhin · Tetrahedron · 1992 · 774 citations
Novel cytotoxic compounds from the ascidian Lissoclinum bistratum
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