Abstract
O-Benzyl-N-arylamidoximes have been regioselectively deprotected to provide either N-aryl amidines or amidoximes. As a result, the targeted compounds can now be prepared using palladium-catalyzed N-arylation chemistry.
Original language | English (US) |
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Pages (from-to) | 9089-9092 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 43 |
Issue number | 50 |
DOIs | |
State | Published - Dec 9 2002 |
Externally published | Yes |
Keywords
- Amidines
- Amidoximes
- HBr/HOAc
- O-benzylamidoximes
- Pd/C/EtOH
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry