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• W2108461755 abstract "Abstract A highly stereoselective total synthesis of attenols A and B is described. The salient features of this synthesis are the utilization of a reductive radical cyclization strategy for methyl center creation, a Prins cyclization/reductive opening cascade for anti ‐1,3‐diol motif generation, and a double alkylation tosylmethyl isocyanide (TosMIC) strategy to construct the spiro acetal segment." @default.
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• W2108461755 date "2013-08-08" @default.
• W2108461755 modified "2023-10-17" @default.
• W2108461755 title "Stereoselective Total Synthesis of Attenols A and B" @default.
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• W2108461755 doi "https://doi.org/10.1002/ejoc.201300623" @default.
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