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Scientific article
English

Asymmetric Dihydroxylations of β-Substituted N-(α,β-Enoyl)bornane-10,2-sultams

Published inHelvetica chimica acta, vol. 70, no. 7, p. 1666-1675
Publication date1987-11-04
First online date2004-10-25
Abstract

Pure (E)- or (Z)-enoylsultams 2 were Oxidized with OsO4/N-Methylmorpholine N-oxide in a stereospecific and highly π-face-selective manner. Acetalization of the resulting 1,2-diols furnished, after purification, the stable, crystalline acetals 6 in >99% d.e. and in 63–74% overall yield from 2. Reductive or hydrolytic cleavage of 6 gave enantiomerically pure alcohols 8 or carboxylic acids 9 with recovery of the sultan auxiliary 1.

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Citation (ISO format)
VON OPPOLZER, Wolfgang, BARRAS, Jean-Pierre. Asymmetric Dihydroxylations of β-Substituted N-(α,β-Enoyl)bornane-10,2-sultams. In: Helvetica chimica acta, 1987, vol. 70, n° 7, p. 1666–1675. doi: 10.1002/hlca.19870700703
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ISSN of the journal0018-019X
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