ChemInform Abstract: Lewis Acid-Catalyzed Meyer—Schuster Reactions: Methodology for the Olefination of Aldehydes and Ketones.
✍ Scribed by Douglas A. Engel; Susana S. Lopez; Gregory B. Dudley
- Publisher
- John Wiley and Sons
- Year
- 2009
- Weight
- 40 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0931-7597
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
Ketene silyl acetals such as (II) and (IV) are added in the presence of various Lewis acids (e.g. (C 6 F 5 ) 2 SnBr 2 ) to ketones with a extremely high level of chemoselectivity in competition with aldehydes or acetales (with exception of benzaldehyde). The generality of ketone preference is also e
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v