2-Phenoxypropene as protective reagent of chiral alcohols

Article abstract of DOI:10.1080/00397919208021543

2-Phenoxypropene (2) was applied as a novel protective reagent of chiral alcohols, yielding 2-phenoxy-isopropyl (PIP) ethers. Introduction and cleavage of the protective group was achieved under mild conditions.

Full text of DOI:10.1080/00397919208021543

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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2-Phenoxypropene as
Protective Reagent of Chiral
Alcohols
P. Zandbergen a , H. M. G. Willems a , G. A. van der
Marel a , J. Brussee a & A. van der Gen a
a Department of Chemistry , Gorlaeus Laboratories,
Leiden University , P.O. Box 9502 2300 RA, Leiden,
The Netherlands
Published online: 23 Sep 2006.
To cite this article: P. Zandbergen , H. M. G. Willems , G. A. van der Marel ,
J. Brussee & A. van der Gen (1992) 2-Phenoxypropene as Protective Reagent
of Chiral Alcohols, Synthetic Communications: An International Journal for
Rapid Communication of Synthetic Organic Chemistry, 22:19, 2781-2787, DOI:
10.1080/00397919208021543
To link to this article: http://dx.doi.org/10.1080/00397919208021543
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