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- W2004328774 abstract "A general strategy for the synthesis of cyclopeptide alkaloids containing an endocyclic aryl-alkyl ether bond has been developed featuring a key intramolecular S(N)Ar reaction. The importance of the N-terminal protective group in the realization of such a strategy is documented. From the appropriate amino acid constituents, the natural sanjoinine G1, a 14-membered para cyclophane, has been synthesized in seven steps with 21% overall yield." @default.
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- W2004328774 date "2002-01-01" @default.
- W2004328774 modified "2023-10-18" @default.
- W2004328774 title "A Convergent Approach to Cyclopeptide Alkaloids: Total Synthesis of Sanjoinine G1" @default.
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- W2004328774 doi "https://doi.org/10.1021/ja0170807" @default.
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