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
β¦ LIBER β¦
ChemInform Abstract: Stereoselective Reduction of Chiral 2-Furoic Acid Derivatives Using Group I Metals in Ammonia.
β Scribed by Timothy J. Donohoe; Andrew A. Calabrese; Clare A. Stevenson; Tamara Ladduwahetty
- Publisher
- John Wiley and Sons
- Year
- 2001
- Weight
- 33 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Abstract
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