A convenient one-pot synthesis of homoallylic halides and 1,3-butadienes
Resource
Tetrahedron Letters (44),8033–8036
Journal
Tetrahedron Letters (44),8033–8036
Pages
-
Date Issued
2003
Date
2003
Author(s)
Hung, Ying-Yueh
DOI
246246/2006111501233421
Abstract
An efficient one-pot synthetic pathway for the preparation of homoallylic halides by in situ generated MgBrCl-promoted
ring opening of cyclopropylcarbinyl acetates has been established. An easily accessible one-pot synthetic protocol of
1,3-butadienes by the elimination of hydrogen halides from the resulting homoallylic halides in the presence of an excess amount
of strong base has also been developed.
Subjects
alcohol
humans
otoacoustic emissions
pure-tone audiometry
Publisher
Taipei:National Taiwan University Dept Chem
Type
journal article
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