Efficient Synthesis of a Novel Estrone- Talaromycin Hybrid Natural Product

Abstract
Numerous pharmacologically interesting compounds are available by the synthesis of hybrid natural products. Thus, for instance, the estrone–talaromycin hybrid 2, which is synthesized in a few steps from the estrone derivative 1 by a sequence in which a hetero-Diels–Alder reaction is the key step, exhibits notable cytotoxic activity.

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