Abnormal birch reduction of dichloro derivatives of C8H10 Hydrocarbons
β Scribed by Charles W. Jefford; Viktor de los Heros
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2010
- Weight
- 162 KB
- Volume
- 88
- Category
- Article
- ISSN
- 0037-9646
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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
Two-dimensional homo-and heteronuclear NMR chemical shift correlation techniques were applied in the characterization of five tricyclic polychlorinated C 10 hydrocarbons, chlordene (1), heptachlor (2), trans-nonachlor (3), Λ-chlordene (4) and -chlordene (5), which are spread globally in the environm
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