Deacylation of Alkyl Carbamates: Selective Deprotection of Secondary Amines
- 1 January 1983
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 13 (2) , 135-138
- https://doi.org/10.1080/00397918308061971
Abstract
Selective deacylation of N,N-disubstituted alkyl carbamates over N-monosubstituted alkyl carbamates can be achieved in excellent yield by the addition of three equivalents of methyl lithium.Keywords
This publication has 2 references indexed in Scilit:
- Synthetic methods and reactions. 62. Transformations with chlorotrimethylsilane/sodium iodide, a convenient in situ iodotrimethylsilane reagentThe Journal of Organic Chemistry, 1979
- Conversion of alkyl carbamates into amines via treatment with trimethylsilyl iodideJournal of the Chemical Society, Chemical Communications, 1978