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Total synthesis of (+/-)-epimagnolin A

Total synthesis of (+/-)-epimagnolin A
Total synthesis of (+/-)-epimagnolin A
The first total synthesis of (±)-epimagnolin A was achieved employing a C-H insertion reaction to generate selectively the bicyclic framework with the exo,endo-stereochemistry.
magnolia-fargesii, flower buds, lignans, neolignans
0040-4039
473-475
Brown, R. C. D.
21ce697a-7c3a-480e-919f-429a3d8550f5
Bataille, C. J. R.
54eb1a97-1963-4ab6-8606-24bfcbd75be7
Hinks, J. D.
8d997f2b-107a-43e5-bb60-828e551105b9
Brown, R. C. D.
21ce697a-7c3a-480e-919f-429a3d8550f5
Bataille, C. J. R.
54eb1a97-1963-4ab6-8606-24bfcbd75be7
Hinks, J. D.
8d997f2b-107a-43e5-bb60-828e551105b9

Brown, R. C. D., Bataille, C. J. R. and Hinks, J. D. (2001) Total synthesis of (+/-)-epimagnolin A. Tetrahedron Letters, 42 (3), 473-475. (doi:10.1016/S0040-4039(00)01958-4).

Record type: Article

Abstract

The first total synthesis of (±)-epimagnolin A was achieved employing a C-H insertion reaction to generate selectively the bicyclic framework with the exo,endo-stereochemistry.

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More information

Published date: 15 January 2001
Keywords: magnolia-fargesii, flower buds, lignans, neolignans

Identifiers

Local EPrints ID: 19433
URI: http://eprints.soton.ac.uk/id/eprint/19433
ISSN: 0040-4039
PURE UUID: e4cee58b-a925-44fd-852e-79a1e348b050
ORCID for R. C. D. Brown: ORCID iD orcid.org/0000-0003-0156-7087

Catalogue record

Date deposited: 14 Feb 2006
Last modified: 16 Mar 2024 02:54

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Contributors

Author: R. C. D. Brown ORCID iD
Author: C. J. R. Bataille
Author: J. D. Hinks

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