Syntheses and biological activity studies of novel sterol analogs from nitroso Diels-Alder reactions of ergosterol.

Syntheses and biological activity studies of novel sterol analogs from nitroso Diels-Alder reactions of ergosterol.
复制标题

DOI:
10.1021/ol900997t
复制
发表时间:
2009-07-02
期刊:
影响因子:
5.2
通讯作者:
Miller MJ
Miller MJ
中科院分区:
化学1区
文献类型:
--
作者:
Yang B;Miller PA;Möllmann U;Miller MJ

文献摘要

参考文献

相似文献

麦角甾醇与亚硝基Diels-Alder反应合成了一系列新的甾醇类似物。大多数环加成反应进行了良好的区域和立体选择性的方式。环加合物的进一步N-O键断裂产生在PC-3和MCF-7癌细胞系中具有生物活性的化合物。
A series of novel sterol analogs was prepared using nitroso Diels-Alder reactions with ergosterol. Most cycloaddition reactions proceeded in an excellent regio- and stereoselective fashion. Further N-O bond cleavage of cycloadducts generated compounds with biological activity in PC-3 and MCF-7 cancer cell lines.
DOI: 10.1021/jo8004827
发表时间: 2008-06-20
影响因子: 3.6
作者:
Krchnak, Viktor;Waring, Katherine R.;Miller, Marvin J.
通讯作者: Miller, Marvin J.
DOI: 10.1016/s0040-4020(01)92150-7
发表时间: 1983-01-01
期刊: TETRAHEDRON
影响因子: 2.1
作者:
MILLER, MJ;BISWAS, A;KROOK, MA
通讯作者: KROOK, MA
DOI: 10.1021/jm00079a012
发表时间: 1992-01-10
影响因子: 7.3
作者:
ATOR, MA;SCHMIDT, SJ;BARONE, JM
通讯作者: BARONE, JM
DOI: 10.1080/mmy.38.s1.335.347
发表时间: 2000-01-01
期刊: MEDICAL MYCOLOGY
影响因子: 2.9
作者:
Walsh, TJ;Viviani, MA;Odds, FC
通讯作者: Odds, FC
DOI: 10.1016/s0968-0896(97)00010-2
发表时间: 1997-05-01
影响因子: 3.5
作者:
AcunaJohnson, AP;Oehlschlager, AC;Czyzewska, EK
通讯作者: Czyzewska, EK