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• W2952713450 abstract "The synthesis and structural analysis, involving X-ray crystallographic, nuclear magnetic resonance, and computational studies of four diastereomers of the common western BCD diarylether macrocycle of the complestatins, a family of HIV entry inhibitors, has been achieved exploiting a ruthenium-promoted intramolecular S(N)Ar reaction. The stereogenicity of the individual phenylglycines (residues C and D) results in remarkable effects on the backbone conformation." @default.
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• W2952713450 date "2004-04-01" @default.
• W2952713450 modified "2023-09-23" @default.
• W2952713450 title "Complestatin synthetic studies" @default.
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• W2952713450 doi "https://doi.org/10.1016/j.bmcl.2004.01.056" @default.
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