Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5333174 | Tetrahedron Letters | 2012 | 4 Pages |
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
Shin-ichi Nakatsuka, Kumi Yoshida, Toshio Goto,