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ChemInform Abstract: Silyl-Substituted Furans in the Stereoselective Birch Reduction.

✍ Scribed by Timothy J. Donohoe; Jean-Baptiste Guillermin; Andrew A. Calabrese; Daryl S. Walter


Publisher
John Wiley and Sons
Year
2010
Weight
29 KB
Volume
32
Category
Article
ISSN
0931-7597

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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

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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 β€œFull Text” option. The original article is trackable v