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Free keywords:
conformation analysis; natural products; NMR spectroscopy; polyketides; residual dipolar coupling
Abstract:
Combine and conquer: Configurational assignment of remote stereogenic centers in the complex polyketide macrolide archazolide A (see structure; red O, blue N, yellow S) was accomplished by a purely NMR-based approach relying on a combination of nuclear Overhauser effects, J couplings, and residual dipolar couplings (RDCs).