| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5217264 | Tetrahedron | 2013 | 4 Pages |
Abstract
Absolute configuration of miyakosyne A at its isolated branched methyl stereogenic center has been studied by chemical degradation in combination with esterification with the Ohrui's acid. Comparison of the 1H NMR data of the relevant diesters for the degradation product and the synthetic standards indicated the 14R-configuration.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Yuki Hitora, Kentaro Takada, Shigeki Matsunaga,