| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5278370 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
Lagunamycin (1) has been synthesized by using our developed remote stereoinduction, Knorr condensation, periodinane oxidation, and diazonation. This enantioselective synthesis determined the absolute configuration of lagunamycin. Existence of rotational conformers was confirmed by NMR studies.
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Authors
Seijiro Hosokawa, Shoichi Kuroda, Keisuke Imamura, Kuniaki Tatsuta,