Asymmetric 1,4-additions to γ-menthyloxybutenolides. Part IV. Two enantioselective syntheses of 2-methyl-1,4-butanediol

Article abstract of DOI:10.1080/00397919208019320

Based on the asymmetric Michael addition to 5(R)- and 5(S)-menthyloxy-2[5H]-furanone two new syntheses of enantiomerically pure R- and S-2-methyl-1,4-butanediol are described.

Full text of DOI:10.1080/00397919208019320

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Synthetic Communications: An
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Asymmetric 1,4-Additions to
Y-Menthyloxybutenolides;
(part IV1) two Enantioselective
Syntheses of 2-Methyl-1,4-
Butanediol
Johan F.G.A. Jansen a & Ben L. Feringa a
a Department of Organic Chemistry , University of
Groningen , Nijenborgh 16, 9747 AG, Groningen, The
Netherlands
Published online: 24 Sep 2006.
To cite this article: Johan F.G.A. Jansen & Ben L. Feringa (1992) Asymmetric 1,4-
Additions to Y-Menthyloxybutenolides;(part IV1) two Enantioselective Syntheses
of 2-Methyl-1,4-Butanediol, Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 22:9, 1367-1376, DOI:
10.1080/00397919208019320
To link to this article: http://dx.doi.org/10.1080/00397919208019320
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