Abstract
The asymmetric synthesis of the marine sponge natural products R-strongylodiols A R- 1 and B R- 2 , using a minimum protection strategy, is described. Two approaches were examined and the Noyori asymmetric reduction of ynones was found to be successful for installing the chirality of the natural products. Analogue R- 32 was also prepared. In addition, asymmetric alkynylation of aldehydes is briefly reviewed.
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