| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5218129 | Tetrahedron | 2013 | 8 Pages |
Abstract
The combination of 1,4-benzoquinone and a catalytic amount of NaI was found to be effective for the deprotection of dithioacetals. The reactions proceeded efficiently under mild, near-neutral reaction conditions, producing a wide range of aryl and alkyl aldehydes and ketones generally in high yields with good functional group compatibility. The method developed therefore represents a general, facile, and highly applicable approach for deprotecting dithioacetals.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Kiyofumi Inamoto, Tetsuya Yamada, Sei-ichi Kato, Shoko Kikkawa, Yoshinori Kondo,