Shoppee et al., Journal of the Chemical Society, 1956, p. 1649,1653
作者:Shoppee et al.
DOI:——
日期:——
Reactions of relevance to the chemistry of aminoglycoside antibiotics. Part 14. A useful radical-deamination reaction
作者:Derek H. R. Barton、Gerhard Bringmann、Genevi�ve Lamotte、William B. Motherwell、Robyn S. Hay Motherwell、Alexander E. A. Porter
DOI:10.1039/p19800002657
日期:——
Primary, secondary, and tertiary aliphatic or alicyclic isocyanides are smoothly reduced under radical conditions using tri-n-butylstannane to the corresponding hydrocarbons. The relative ease of reduction is tertiary > secondary > primary. Aromatic isocyanides are not reduced under these conditions. The reduction of isothiocyanates (or isoselenocyanates) by tri-n-butylstannane also affords hydrocarbons
Treatment of various alcohols with 1-methyl-2-fluoropyridinium salt and lithium azide afforded corresponding alkyl azides, which were converted to primaryamines by reduction. The overall reactions proceeded with inversion of configuration.