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Stereoselectivity in the Birch reduction of 2-furoic acid derivatives

✍ Scribed by Timothy J Donohoe; Madeleine Helliwell; Clare A Stevenson; Tamara Ladduwahetty

Publisher
Elsevier Science
Year
1998
Tongue
French
Weight
241 KB
Volume
39
Category
Article
ISSN
0040-4039

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πŸ“œ SIMILAR VOLUMES

ChemInform Abstract: Stereoselectivity i
ChemInform Abstract: Stereoselectivity in the Birch Reduction of 2-Furoic Acid Derivatives.
✍ T. J. DONOHOE; M. HELLIWELL; C. A. STEVENSON; T. LADDUWAHETTY πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 31 KB πŸ‘ 2 views

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

ChemInform Abstract: Stereoselective Red
ChemInform Abstract: Stereoselective Reduction of Chiral 2-Furoic Acid Derivatives Using Group I Metals in Ammonia.
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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

The birch reduction of heterocyclic comp
The birch reduction of heterocyclic compounds. III. Birch reduction-elimination reaction of 2- and 3-furancarboxylic acid derivatives
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## Abstract The Birch reduction of 2‐(1‐alkoxyalkyl)furan‐3‐carboxylic acids 1a‐f gave 2‐alkyl‐3‐furancarboxylic acids 2a‐f with loss of the alkoxyl group in excellent isolated yields.