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Merck

Total synthesis of paracaseolide A.

Organic letters (2013-01-18)
Tezcan Guney, George A Kraus
ABSTRACT

The total synthesis of paracaseolide A, a valuable cell-cycle progression inhibitor, was accomplished in 8 steps from known compounds, with 6.6% overall yield. The synthetic strategy creates strong potential for diversification.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
4-Hydroxybutanoic acid lactone, ≥98%, FCC, FG
Sigma-Aldrich
γ-Butyrolactone, ReagentPlus®, ≥99%