- Towards the Total Synthesis of 3-Hydroxyvibsanin E
[作者:SCHWARTZ BRETT D; DENTON JUSTIN R; BERNHARDT PAUL V; DAVIES HUW M L; WILLIAMS CRAIG M,期刊:Synthesis, 页码:2840-2846 , 文章类型: Article,,卷期:2009年-17]
- The synthesis of a silyl-protected derivative of 3-hydroxyvibsanin E has been achieved. The key step is a regio- and stereoselective C-H hydroxylation of an advanced tricyclic intermediate by means of a Rubottom oxidatio...
- Formal Total Synthesis of Palmerolide A
[作者:JAEGEL JULIA; MAIER MARTIN E,期刊:Synthesis, 页码:2881-2892 , 文章类型: Article,,卷期:2009年-17]
- A concise route to macrolactone 38, an advanced intermediate of the Nicolaou/Chen synthesis of palmerolide A, is described. Key steps in our synthesis include a Noyori transfer hydrogenation of all alkynone, chain extens...
- Second-Generation, Biomimetic Total Synthesis of Chaetominine
[作者:COSTE ALEXIS; KARTHIKEYAN GANESAN; COUTY FRANCOIS; EVANO GWILHERM,期刊:Synthesis, 页码:2927-2934 , 文章类型: Article,,卷期:2009年-17]
- A straightforward total synthesis of the potent anticancer agent (-)-chaetominine is reported. Central to this synthesis was a biomimetic oxidative cyclization of a tryptophanyl-alanine dipeptide, which provided a fully ...
- Total Synthesis of (+)-Fostriecin and (+)-Phoslactomycin B
[作者:SHIBAHARA SETSUYA; FUJINO MASATAKA; TASHIRO YASUMASA; OKAMOTO NANAKO; ESUMI TOMOYUKI; TAKAHASHI KEISUSKE; ISHIHARA JUN; HATAKEYAMA SUSUMI,期刊:Synthesis, 页码:2935-2953 , 文章类型: Article,,卷期:2009年-17]
- (+)-Fostriecin and (+)-phoslactornycin B, which are potent and selective inhibitors of protein phosphatase, were synthesized by a highly enantio- and stereoselective approach that enabled us to prepare all possible isome...
- Formal Synthesis of Salinosporamide A Starting from D-Glucose
[作者:MOMOSE TAKAYUKI; KAIYA YUJI; HASEGAWA JUNICHI; SATO TAKAAKI; CHIDA NORITAKA,期刊:Synthesis, 页码:2983-2991 , 文章类型: Article,,卷期:2009年-17]
- A formal synthesis of salinosporarmde A is described. The tertiary alcohol function in salinosporarmde A was stereoselectively generated via the substrate control by the reaction of a cyclic ketone derived from D-glucose...
- Total Synthesis of the Leucetta-Derived Alkaloid Calcaridine A
[作者:KOSWATTA PANDUKA B; SIVAPPA RASAPALLI; DIAS H V RASIKA; LOVELY CARL J,期刊:Synthesis, 页码:2970-2982 , 文章类型: Article,,卷期:2009年-17]
- A biomimetically guided total synthesis of the Leucetta-derived aminoimidazole alkaloid, calcaridine A, is described. The synthesis relies on position selective metalations of a 4,5-diiodoimidazole derivative to provide ...
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