| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5270550 | Tetrahedron Letters | 2009 | 7 Pages |
Abstract
The total synthesis of clemochinenoside A and the first total syntheses of clemochinenoside B and berchemolide were achieved simultaneously via macrocyclization of 4-O-(4-O-F13benzyl-β-d-glucopyranosyl)syringic acid with 4-O-(4-O-F17benzyl-β-d-glucopyranosyl)vanillic acid by a fluorous mixture synthetic method. The spectroscopic data of the synthetic products were identical with those of the natural products, although the optical rotation of clemochinenoside A differed from the published values in sign and magnitude.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Masaru Kojima, Yutaka Nakamura, Shun Ito, Seiji Takeuchi,
