This review uncovers enantioselective strategies for synthesizing various spiroketal types, highlighting critical catalytic methods.
This review highlights enantioselective strategies for preparing (N,O)- (N,N)- and (N,S)-spiroketal skeleton, which are key structural units found in many natural products and pharmacologically active substances. The strategies are mainly based on metallo-, organo- or Lewis acid-catalyzed cycloaddition or annulation reactions.
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Sow et al. (2025) studied this question.
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