The Lewis acid mediated cyclization of β-oxygen substituted allylic stannanes 1,2, and 9, bearing a hydrazone group at the terminus of the carbon chain, afforded the corresponding trans-β-amino cyclic ethers 3a,4a and 10, respectively, with very high diastereoselectivities in high chemical yields.
I. Kadota, J. Park and Y. Yamamoto, Chem. Commun., 1996, 841 DOI: 10.1039/CC9960000841
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