| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5223627 | Tetrahedron | 2008 | 5 Pages |
Abstract
Two antifungal phthalides produced by a wheat rhizosphere fungus have been synthesized using the Alder-Rickert reaction to construct their common isobenzofuranone core structure. The absolute configuration of one of the two phthalides has been determined to be S by synthesizing its (S)- and (R)-enantiomer and comparing their optical rotations with that of the natural product.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Naoto Katoh, Takashi Nakahata, Shigefumi Kuwahara,