Synthesis of 1,2-aminoazides. Conversion to unsymmetrical vicinal diamines by catalytic hydrogenation or reductive alkylation with dichloroboranes.
- 1 September 1991
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 47 (38) , 8177-8194
- https://doi.org/10.1016/s0040-4020(01)91013-0
Abstract
No abstract availableThis publication has 69 references indexed in Scilit:
- New chiral bicyclic phosphoramides derived from (L)-glutamic acidThe Journal of Organic Chemistry, 1987
- Efficient one-step synthesis of a cis vicinal tertiary diamine and its complexation to a lithium carbanion saltThe Journal of Organic Chemistry, 1984
- A One-Pot Synthesis of Aziridines from 2-AminoethanolsSynthesis, 1984
- Bledta II: Synthesis of a new tumor‐visualizing derivative of CO(III)‐bleomycinJournal of Labelled Compounds and Radiopharmaceuticals, 1981
- Mechanism of the photoreduction of N-AlkylbenzylideniminesJournal of the American Chemical Society, 1969
- Preparation and Polymerization of D- and L-Propylenimine and N-Methylpropylenimine1Journal of the American Chemical Society, 1959
- Tetraalkyloxamides and their Reduction to N,N,-N',N'-Tetraalkylethylenediamines1Journal of the American Chemical Society, 1953
- N,N'-Dialkylethylenediamines by Reduction of Dialkyloxamides1a,bJournal of the American Chemical Society, 1953
- β-Dialkylaminoethyl Bromide Hydrobromides and β-Dialkylaminoethylamines1Journal of the American Chemical Society, 1941
- α-Aryl-β-dialkylaminoalkyl Ureas as Local AnestheticsJournal of the American Chemical Society, 1938