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Aldol elaboration of 4,5,6,7-tetrahydroisoxazolo[4,3-c]pyridin-4-ones, masked precursors to acylpyridones
- Source :
- Beilstein Journal of Organic Chemistry, Vol 8, Iss 1, Pp 308-312 (2012), Beilstein Journal of Organic Chemistry
- Publication Year :
- 2012
- Publisher :
- Beilstein-Institut, 2012.
-
Abstract
- A core 4,5,6,7-tetrahydroisoxazolo[4,3-c]pyridine-4-one scaffold is elaborated at C-3(Me) by base-mediated aldol condensation to give new 3-alkenyl-4,5,6,7-tetrahydroisoxazolo[4,3-c]pyridine-4-ones, which are masked forms related to the acylpyridone natural products.
- Subjects :
- heterocycles
Metalation
Organic Chemistry
isoxazole
metalation
pyridone
Full Research Paper
fused-ring systems
lcsh:QD241-441
Chemistry
chemistry.chemical_compound
Aldol reaction
chemistry
lcsh:Organic chemistry
Organic chemistry
aldol reaction
Aldol condensation
lcsh:Q
Isoxazole
lcsh:Science
Elaboration
Subjects
Details
- Language :
- English
- ISSN :
- 18605397
- Volume :
- 8
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Beilstein Journal of Organic Chemistry
- Accession number :
- edsair.doi.dedup.....f9030705078aeebcb94610afb8b871a7