Polytopic bis(oxazoline)-based ligands for the development of recoverable catalytic systems applied to the cyclopropanation reaction
New ditopic and tetratopic chiral ligands, based on the bis(oxazoline) moiety, have been synthesized and their copper complexes tested as catalysts in the benchmark asymmetric cyclopropanation reaction of styrene with ethyl diazoacetate. The polytopic nature of these ligands enables a release-captur...
| Authors: | , , , , , |
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| Format: | article |
| Status: | Versión aceptada para publicación |
| Publication Date: | 2014 |
| Country: | España |
| Institution: | Consejo Superior de Investigaciones Científicas (CSIC) |
| Repository: | DIGITAL.CSIC. Repositorio Institucional del CSIC |
| OAI Identifier: | oai:digital.csic.es:10261/111658 |
| Online Access: | http://hdl.handle.net/10261/111658 |
| Access Level: | Open access |
| Keyword: | Coordination polymers Enantioselectivity Self-supported catalysts Polytopic ligands Copper Polymerization |
| Summary: | New ditopic and tetratopic chiral ligands, based on the bis(oxazoline) moiety, have been synthesized and their copper complexes tested as catalysts in the benchmark asymmetric cyclopropanation reaction of styrene with ethyl diazoacetate. The polytopic nature of these ligands enables a release-capture strategy to efficiently recycle the enantioselective catalyst by precipitation of a coordination polymer at the end of the reaction. This strategy enables the self-supported catalyst to be reused up to 20 times leading to good yields and enantioselectivities. |
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