Total synthesis of (-)- and (+)-dysibetaine |
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Authors: | Snider B B Gu Y |
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Affiliation: | Department of Chemistry, MS015, Brandeis University, Waltham, Massachusetts 02454-9110, USA. snider@brandeis.edu |
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Abstract: | Glycidamides 6R and 6S were elaborated to (R,R)- and (S,S)-dysibetaines (1R and 1S) by intramolecular alkylation and functional group modification in 23% overall yield. The absolute stereochemistry of natural dysibetaine was established as S,S by comparison of the optical rotation of the natural product with that of the synthetic materials. |
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