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C-3 Acetoxylation of N-acyl-2,3-dihydro-4-pyridones

✍ Scribed by Daniel L. Comins; David A. Stolze; Faresh Thakker; Cheryl L. McArdle

Book ID
108386923
Publisher
Elsevier Science
Year
1998
Tongue
French
Weight
190 KB
Volume
39
Category
Article
ISSN
0040-4039

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ChemInform Abstract: C-3 Acetoxylation o
ChemInform Abstract: C-3 Acetoxylation of N-Acyl-2,3-dihydro-4-pyridones.
✍ D. L. COMINS; D. A. STOLZE; P. THAKKER; C. L. MCARDLE πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 28 KB πŸ‘ 2 views

C-3 Acetoxylation of N-Acyl-2,3-dihydro-4-pyridones. -Stereoselective C-3 acetoxylation of various N-acyldihydropyridones (I) is achieved under mild conditions using lead tetraacetate. The analogous reaction of the indolizidinone (IV) to the cis product proceeds with considerably lower yield.