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Synthesis, resolution and crystallographic characterization of a new C2-symmetric planar-chiral bipyridine ligand: application to the catalytic enantioselective cyclopropanation of olefins

Synthesis, resolution and crystallographic characterization of a new C2-symmetric planar-chiral bipyridine ligand: application to the catalytic enantioselective cyclopropanation of olefins
Synthesis, resolution and crystallographic characterization of a new C2-symmetric planar-chiral bipyridine ligand: application to the catalytic enantioselective cyclopropanation of olefins
The synthesis of a new C2-symmetric planar-chiral bipyridine ligand is described, as well as its application to the enantioselective CuI-catalyzed cyclopropanation of olefins.
1359-7345
377-378
Rios, Ramon
609bedf2-e886-4d62-a676-a32b6f8c1441
Liang, Jack
fc497805-e5d5-41cd-aa1a-05618d742a47
Lo, Michael M.-C.
699daab5-ea4c-4fb8-bf2b-f4d36339b572
Fu, Gregory C.
853ab042-6c2d-4b2c-8d7f-201d88f459ec
Rios, Ramon
609bedf2-e886-4d62-a676-a32b6f8c1441
Liang, Jack
fc497805-e5d5-41cd-aa1a-05618d742a47
Lo, Michael M.-C.
699daab5-ea4c-4fb8-bf2b-f4d36339b572
Fu, Gregory C.
853ab042-6c2d-4b2c-8d7f-201d88f459ec

Rios, Ramon, Liang, Jack, Lo, Michael M.-C. and Fu, Gregory C. (2000) Synthesis, resolution and crystallographic characterization of a new C2-symmetric planar-chiral bipyridine ligand: application to the catalytic enantioselective cyclopropanation of olefins. Chemical Communications, 377-378. (doi:10.1039/A909457A).

Record type: Article

Abstract

The synthesis of a new C2-symmetric planar-chiral bipyridine ligand is described, as well as its application to the enantioselective CuI-catalyzed cyclopropanation of olefins.

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More information

Published date: 22 February 2000
Organisations: Chemistry

Identifiers

Local EPrints ID: 348004
URI: http://eprints.soton.ac.uk/id/eprint/348004
ISSN: 1359-7345
PURE UUID: 8eabc8b0-748c-4156-8e70-c2de0ce048b6
ORCID for Ramon Rios: ORCID iD orcid.org/0000-0002-3843-8521

Catalogue record

Date deposited: 05 Feb 2013 11:35
Last modified: 10 Dec 2019 01:37

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