Article ID Journal Published Year Pages File Type
5333174 Tetrahedron Letters 2012 4 Pages PDF
Abstract
Regiospecific cyclization of the alcohol 8 into the bicyclo[ 4.2.2] compound 12 was achieved via selective activation of the secondary methoxy group and subsequent acid treatment. A side-chain was introduced at the bridge-head position, thus making up the bicyclomycin skeleton.
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Authors
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