Abstract
α-Methoxybenzamides 11, which are convenient precursors of acyclic N-acylimines, can be cleanly generated in high yields via a free radical process starting from an o-aminobenzamide 16 derived from an N-t-butyl or N-cumyl secondary amine. (C) 2000 Elsevier Science Ltd.
Original language | English (US) |
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Pages (from-to) | 9199-9204 |
Number of pages | 6 |
Journal | Tetrahedron Letters |
Volume | 41 |
Issue number | 48 |
DOIs | |
State | Published - Nov 25 2000 |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Drug Discovery
- Organic Chemistry