Self-Assembly of Bidentate Ligands for Combinatorial Homogeneous Catalysis: Methanol-Stable Platforms Analogous to the Adenine-Thymine Base Pair

Complementary partners: A combinatorial library of self‐assembled ligand systems has been designed by analogy to the A–T base pair. When these ligand systems are applied in the rhodium‐catalyzed hydroformylation of 1‐octene (see scheme), high regioselectivities (rs) are obtained, even in the protic...

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Veröffentlicht in:Angewandte Chemie International Edition 2007-01, Vol.46 (17), p.3037-3039
Hauptverfasser: Waloch, Christoph, Wieland, Jörg, Keller, Manfred, Breit, Bernhard
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container_issue 17
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container_title Angewandte Chemie International Edition
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creator Waloch, Christoph
Wieland, Jörg
Keller, Manfred
Breit, Bernhard
description Complementary partners: A combinatorial library of self‐assembled ligand systems has been designed by analogy to the A–T base pair. When these ligand systems are applied in the rhodium‐catalyzed hydroformylation of 1‐octene (see scheme), high regioselectivities (rs) are obtained, even in the protic solvent methanol.
doi_str_mv 10.1002/anie.200605202
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subjects Adenine - analogs & derivatives
Adenine - chemistry
Base Pairing
Catalysis
combinatorial chemistry
homogeneous catalysis
hydroformylation
Ligands
Magnetic Resonance Spectroscopy
Methanol - chemistry
Molecular Structure
rhodium
self-assembly
Thymine - analogs & derivatives
Thymine - chemistry
title Self-Assembly of Bidentate Ligands for Combinatorial Homogeneous Catalysis: Methanol-Stable Platforms Analogous to the Adenine-Thymine Base Pair
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