[reaction: see text] A new diastereoselective synthesis of pyrrolidines from readily available chiral N-allyl oxazolidines is presented. The construction of the pyrrolidine ring is achieved via a tandem hydrozirconation-stereoselective Lewis acid mediated cyclization sequence.
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| http://dx.doi.org/10.1021/ol0517776 | DOI Listing |
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text] diastereoselective
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