Allenyloxime—a new source of heterocyclizations to stable cyclic nitrones
摘要:
A variety of conditions including reductive and/or basic reagents in aqueous or alcoholic solution was applied to 2,2-dimethylpenta-3,4-dienal oxime. Formation of various five-membered heterocycles with excellent chemical selectivity was observed. Most of the reactions yielded cyclic nitrones with stable dipolar structure and unique functionalities present. All products of cyclization were isolated and fully characterized. (C) 2008 Elsevier Ltd. All rights reserved.
Allenyloxime—a new source of heterocyclizations to stable cyclic nitrones
摘要:
A variety of conditions including reductive and/or basic reagents in aqueous or alcoholic solution was applied to 2,2-dimethylpenta-3,4-dienal oxime. Formation of various five-membered heterocycles with excellent chemical selectivity was observed. Most of the reactions yielded cyclic nitrones with stable dipolar structure and unique functionalities present. All products of cyclization were isolated and fully characterized. (C) 2008 Elsevier Ltd. All rights reserved.
Allenyloxime—a new source of heterocyclizations to stable cyclic nitrones
作者:Marian Buchlovič、Stanislav Man、Milan Potáček
DOI:10.1016/j.tet.2008.07.113
日期:2008.10
A variety of conditions including reductive and/or basic reagents in aqueous or alcoholic solution was applied to 2,2-dimethylpenta-3,4-dienal oxime. Formation of various five-membered heterocycles with excellent chemical selectivity was observed. Most of the reactions yielded cyclic nitrones with stable dipolar structure and unique functionalities present. All products of cyclization were isolated and fully characterized. (C) 2008 Elsevier Ltd. All rights reserved.