Stereoselective synthesis of a novel branched-chain (1S,2R,6R,7S)-7a-(hydroxymethyl)-1,2,6,7-tetrahydroxypyrrolizidine
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文摘

A convenient approach to a new type of branched-chain pentahydroxylated pyrrolizidine.

Ring closing metathesis of a diene-substrate foldamer possessing the amino functionality.

The spontaneous cyclisation during regioselective tosylation to establish a pyrrolizidine unit.

Highly substrate-controlled diastereoselective dihydroxylation.

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