A series of new chiral binol based [1+1] macrocyclic Schiff bases have been synthesized in high yields in short reaction times via cyclo-condensation of dialdehydes with long tethers and chiral diamines. Macrocyclic Mn(salen) complexes containing N2O2 salen units incorporated with spacers of increased tether lengths were synthesized and characterized. The newly synthesized catalyst system was successfully employed for the enantioselective epoxidation of unfunctionalized olefins with high yields and good enantioselectivity. (C) 2013 Elsevier Ltd. All rights reserved.
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IBM Corp, Almaden Res Ctr, Div Res, Ctr Polymer Interfaces & Macromol Assemblies, San Jose, CA 95120 USAIBM Corp, Almaden Res Ctr, Div Res, Ctr Polymer Interfaces & Macromol Assemblies, San Jose, CA 95120 USA
Dao, J
Benoit, D
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IBM Corp, Almaden Res Ctr, Div Res, Ctr Polymer Interfaces & Macromol Assemblies, San Jose, CA 95120 USAIBM Corp, Almaden Res Ctr, Div Res, Ctr Polymer Interfaces & Macromol Assemblies, San Jose, CA 95120 USA
Benoit, D
Hawker, CJ
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IBM Corp, Almaden Res Ctr, Div Res, Ctr Polymer Interfaces & Macromol Assemblies, San Jose, CA 95120 USAIBM Corp, Almaden Res Ctr, Div Res, Ctr Polymer Interfaces & Macromol Assemblies, San Jose, CA 95120 USA
LIU XinWen Tang Ning College of Chemistry and Chemical Engineering Lanzhou University Lanzhou China College of Life Sciences and Chemistry Tianshui Normal University Tianshui China
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LIU XinWen Tang Ning College of Chemistry and Chemical Engineering Lanzhou University Lanzhou China College of Life Sciences and Chemistry Tianshui Normal University Tianshui China