Stereoselective construction of quaternary centers at ambient temperature by the highly stereocontrolled migration of groups containing sp-, sp2-, and sp3-hybridized …

…, J Pickering, AD Hobson, R Wrigglesworth…

Index: Marson, Charles M.; Walker, Andrew J.; Pickering, Jane; Hobson, Adrian D.; Wrigglesworth, Roger; Edge, Simon J. Journal of Organic Chemistry, 1993 , vol. 58, # 22 p. 5944 - 5951

Full Text: HTML

Citation Number: 64

Abstract

A very highly diastereoselective semipinacol rearrangement of 2, 3-epoxy alcohols mediated by tin-(IV) chloride at ambient temperatures is shown to be applicable to a wide variety of migrating groups including methyl, tert-butyl, cyclopropy1, vinyl, alkynyl, phenyl, and 2-furyl. A synthetically valuable feature is that a mixture of syn-and anti-epoxy alcohols affords only a single diastereoisomerically pure 8-hydroxy ketone. Additional advantages ...

Related Articles:

New cross-aldol reactions. Reactions of silyl enol ethers with carbonyl compounds activated by titanium tetrachloride

[Mukaiyama,T. et al. Journal of the American Chemical Society, 1974 , vol. 96, p. 7503 - 7509]

Titanocene-Promoted Intermolecular Couplings of Epoxides with Nitriles. An Easy Access to β-Hydroxyketones

[Fernandez-Mateos; Encinas Madrazo; Herrero Teijon; Rubio Gonzalez Journal of Organic Chemistry, 2009 , vol. 74, # 10 p. 3913 - 3918]

More Articles...