ChemInform Abstract: The Stereoselective Birch Reduction of Pyrroles.
β Scribed by Timothy J. Donohoe; Paul M. Guyo; Madeleine Helliwell
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 29 KB
- Volume
- 30
- 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 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
Stereoselectivity in the Birch Reduction of 2-Furoic Acid Derivatives. -Birch reduction of the chiral amide (I) of 2-furoic acid and following electrophilic quench gives the dihydrofuroic amides (III) with high diastereoselectivity. Acidic cleavage of the chiral auxiliary liberates the carboxylic a