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An unexpected product from attempted reductive etherification of a silyl alcohol with an aldehyde
Authors:Christopher G.H. White
Affiliation:Department of Chemistry, UCL, 20, Gordon Street, London WC1H 0AJ, UK
Abstract:
Reductive etherification, using BiBr3/Et3SiH, between two modified amino acids, one with a silyl alcohol side chain and one with an aldehyde side chain, gave, not the desired bis-amino acid, but a tetrahydrooxazine, in good yield.
Keywords:Reductive etherification   Cyclic aminal
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