Teleocidin B analogs have been synthesized in 24 steps and 1.9% overall yield. The key steps include aromatic Claisen rearrangement, intramolecular Heck reaction of a tetra-substituted alkene, and ruthenium (II) catalyzed indole cyclization. Teleocidin and the new analogs promote cell spreading on fibroblast cells that were treated with amino-Nogo, an inhibitor of cell spreading. (C) 2010 Elsevier Ltd. All rights reserved.
Teleocidin B analogs have been synthesized in 24 steps and 1.9% overall yield. The key steps include aromatic Claisen rearrangement, intramolecular Heck reaction of a tetra-substituted alkene, and ruthenium (II) catalyzed indole cyclization. Teleocidin and the new analogs promote cell spreading on fibroblast cells that were treated with amino-Nogo, an inhibitor of cell spreading. (C) 2010 Elsevier Ltd. All rights reserved.
作者:I. Yu. Chukicheva、I. V. Fedorova、Т. А. Kolegova、A.V. Kutchin
DOI:10.1134/s1070363220030032
日期:2020.3
AbstractOrganoaluminum (aluminum phenolate and aluminumisopropylate) and acidic heterogeneous catalysts (zeolites C-10, C-100 and ZSM, clay KSF, sulfonic cation exchangers Fiban K-1 and Amberlist 36 Dry) were studied in the alkylation of 4-methylphenol with prenol. Effective catalysts and conditions for the synthesis of 4-methyl-2-prenylphenol, 2,6-diprenyl-4-methylphenol, and chromane were revealed
Teleocidin B analogs have been synthesized in 24 steps and 1.9% overall yield. The key steps include aromatic Claisen rearrangement, intramolecular Heck reaction of a tetra-substituted alkene, and ruthenium (II) catalyzed indole cyclization. Teleocidin and the new analogs promote cell spreading on fibroblast cells that were treated with amino-Nogo, an inhibitor of cell spreading. (C) 2010 Elsevier Ltd. All rights reserved.