The 2,3,4,4a,5, isoquinoline-7(7aH)-one ring system is prepared from a 4-arylpyridine precursor by sequential intramolecular enolate addition to a pyridinium ion, Dieckmann cyclization, and catalytic hydrogenation.
An Experimental and Theoretical Study of the Asymmetric Lithiation of 1,2,3,5,6,7-Hexahydro-3a,4a-diazacyclopenta[ def ]phenanthren-4-one
β Scribed by Metallinos, Costa; Dudding, Travis; Zaifman, Josh; Chaytor, Jennifer L.; Taylor, Nicholas J.
- Book ID
- 126094849
- Publisher
- American Chemical Society
- Year
- 2007
- Tongue
- English
- Weight
- 240 KB
- Volume
- 72
- Category
- Article
- ISSN
- 0022-3263
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