Acylation of 2-benzylpyridine N-oxides and subsequent in situ [3,3]-sigamatropic rearrangement reaction
作者:Hua-qing Jing、Hong-liang Li、Jon C. Antilla
DOI:10.1016/j.tetlet.2020.152401
日期:2020.10
2-benzylpyridine N-oxides and their fast in situ [3,3]-sigmatropic rearrangement was reported. This transformation has a wide substrate scope under mild conditions, giving moderate to excellent yields. The application for the synthesis of chiral phenyl-2-pyridylmethanol products was briefly explored. Furthermore, an interesting example of tandem substitution and in situ [3,3]-sigamatropic rearrangement of 2-benzylpyridine
FLASH VACUUM PYROLYSIS OF 2-BENZYLPYRIDINE<i>N</i>-OXIDES. SYNTHESIS OF METHYLPYRIDO[1,2-<i>a</i>]INDOLES
作者:Akio Ohsawa、Takayuki Kawaguchi、Hiroshi Igeta
DOI:10.1246/cl.1981.1737
日期:1981.12.5
Flashvacuumpyrolysis of 2-benzylpyridine N-oxides afforded pyrido[1,2-a]-indole and its various methyl-substituted derivatives in moderate yields. Benzo[g]quinoline in the pyrolyses of 2-(o-methylbenzyl)pyridine N-oxide and 2-benzyl-3-methylpyridine Noxide, and 2-(β-styryl)pyridine in the reaction of 2-(β-phenethyl)pyridine N-oxide were major products as exceptional cases.