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An enantioselective desymmetrisation approach to C9-substituted trans-hydrindene rings based on a diastereotopic group-selective intramolecular Dield-Alder reaction

An enantioselective desymmetrisation approach to C9-substituted trans-hydrindene rings based on a diastereotopic group-selective intramolecular Dield-Alder reaction
An enantioselective desymmetrisation approach to C9-substituted trans-hydrindene rings based on a diastereotopic group-selective intramolecular Dield-Alder reaction
The synthesis of an achiral skipped bis(1,3-diene) substrate was achieved, which was shown to undergo an enantioselective, diastereotopic group-selective, intramolecular Diels–Alder reaction.
1359-7345
4909-4911
Azzi, Nadia
bab2c9e3-a4ba-4bb4-b184-010e279fb006
Griffen, Ed
0a8546b3-ebb1-44f4-8410-53730d606db5
Light, Mark
cf57314e-6856-491b-a8d2-2dffc452e161
Linclau, Bruno
19b9cacd-b8e8-4c65-af36-6352cade84ba
Azzi, Nadia
bab2c9e3-a4ba-4bb4-b184-010e279fb006
Griffen, Ed
0a8546b3-ebb1-44f4-8410-53730d606db5
Light, Mark
cf57314e-6856-491b-a8d2-2dffc452e161
Linclau, Bruno
19b9cacd-b8e8-4c65-af36-6352cade84ba

Azzi, Nadia, Griffen, Ed, Light, Mark and Linclau, Bruno (2006) An enantioselective desymmetrisation approach to C9-substituted trans-hydrindene rings based on a diastereotopic group-selective intramolecular Dield-Alder reaction. Chemical Communications, 2006 (47), 4909-4911. (doi:10.1039/b607488j).

Record type: Article

Abstract

The synthesis of an achiral skipped bis(1,3-diene) substrate was achieved, which was shown to undergo an enantioselective, diastereotopic group-selective, intramolecular Diels–Alder reaction.

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Published date: 2006

Identifiers

Local EPrints ID: 43294
URI: https://eprints.soton.ac.uk/id/eprint/43294
ISSN: 1359-7345
PURE UUID: 4d65adc3-6526-420d-bd1d-1da1b29eb708
ORCID for Mark Light: ORCID iD orcid.org/0000-0002-0585-0843
ORCID for Bruno Linclau: ORCID iD orcid.org/0000-0001-8762-0170

Catalogue record

Date deposited: 22 Jan 2007
Last modified: 14 Mar 2019 01:48

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Contributors

Author: Nadia Azzi
Author: Ed Griffen
Author: Mark Light ORCID iD
Author: Bruno Linclau ORCID iD

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