Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5216861 | Tetrahedron | 2014 | 6 Pages |
Abstract
The first total synthesis of the marine natural product (+)-hemifistularin 3 in enantiomerically pure form was accomplished by using the amide forming reaction of (+)-spiroisoxazoline ester with the (+)-octopamine derivative. The stereodivergent strategy employed in this effort enabled the assignment of the absolute configurations at the three stereogenic centers in (+)-hemifistularin 3.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Hironori Kubo, Kaori Matsui, Tsuyoshi Saitoh, Shigeru Nishiyama,