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Palladium mediated regioselective intramolecular Heck reaction: synthesis of 1,3,4-trisubstituted pyrazolo[3,4-b]pyridines, 3H-pyrazolo[3,4-c]isoquinolines and 3H-pyrazolo[4,3-f][1,7]naphthyridines
An efficient method was developed for the synthesis of 1,3,4-trisubstituted pyrazolo[3,4- b ]pyridines, 3 H -pyrazolo[3,4- c ]isoquinolines and 3 H -pyrazolo[4,3- f ][1,7]naphthyridines via intramolecular Heck reactions of imine derivatives of β-halovinyl/aryl aldehydes and 5-aminopyrazoles. This pa...
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Published in: | RSC advances 2015, Vol.5 (27), p.21099-21102 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | An efficient method was developed for the synthesis of 1,3,4-trisubstituted pyrazolo[3,4-
b
]pyridines, 3
H
-pyrazolo[3,4-
c
]isoquinolines and 3
H
-pyrazolo[4,3-
f
][1,7]naphthyridines
via
intramolecular Heck reactions of imine derivatives of β-halovinyl/aryl aldehydes and 5-aminopyrazoles. This palladium acetate catalyzed reaction afforded good yields of these pyrazolo fused compounds under thermal conditions in the presence of xantphos as the ligand. |
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ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/C4RA17190J |