| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5275699 | Tetrahedron Letters | 2008 | 5 Pages |
Abstract
The enantioselective synthesis of trimethyl octa-O-methylvaloneate (1) was accomplished using the Bringmann's 'lactone concept', which involves the intramolecular biaryl coupling reaction of a phenyl benzoate derivative and the asymmetric lactone-opening reaction.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Hitoshi Abe, Yusuke Sahara, Yuki Matsuzaki, Yasuo Takeuchi, Takashi Harayama,