作者:M. A. Bastrakov、A. M. Starosotnikov、I. V. Glukhov、S. A. Shevelev
DOI:10.1007/s11172-010-0027-1
日期:2009.2
A method was developed for the selective amination of 3-R-4,6-dinitrobenzo[d]isoxazoles at position 7 via the oxidative nucleophilic substitution of hydrogen. The resulting nitroamines were used to synthesize representatives of the previously unknown tricyclic heteroaromatic system, viz., isoxazolo[5,4-e]benzofuroxan.
开发了一种通过
氢的
氧化亲核取代在 7 位选择性胺化 3-R-4,6-
二硝基苯并[d]
异恶唑的方法。所得
硝基胺用于合成以前未知的
三环杂芳族系统的代表,即异恶唑并[5,4-e]
苯并呋喃。