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Selective Monoacylation of a Diamine Using Intramolecular Delivery by a DMAP Unit
1E. F. Merkert Chemistry Center, Boston College, Chestnut Hill, Massachusetts 02467, USA. ross.kelly@bc.edu
Organic Letters
|August 3, 2002
Abstract:
[reaction: see text] Regioselective monoacylation of a diamine is achieved by including a suitably positioned 4-(dimethylamino)pyridine (DMAP) group within the molecule.