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(1S*,4S*,5R*,8R*)-4,8-Diphenyl-3,7-dioxa- bicyclo[3.3.0] octan-2-one

(1S*,4S*,5R*,8R*)-4,8-Diphenyl-3,7-dioxa- bicyclo[3.3.0] octan-2-one
(1S*,4S*,5R*,8R*)-4,8-Diphenyl-3,7-dioxa- bicyclo[3.3.0] octan-2-one
The title compound, C18H16O3, (I), was prepared in the course of studies towards the synthesis of furofuran ligands and was reported previously [Brown & Hinks (1998). Chem. Commun. pp. 1895-1896]. The compound is a a model system, where both oxygenated aromatic rings that are present in the natural products have been substituted by a simple phenyl group.
o566-o567
Gelbrich, T.
42309d69-eaf1-4bb7-ba2e-db61f338e370
Hursthouse, M.B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Gelbrich, T.
42309d69-eaf1-4bb7-ba2e-db61f338e370
Hursthouse, M.B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da

Gelbrich, T. and Hursthouse, M.B. (2001) (1S*,4S*,5R*,8R*)-4,8-Diphenyl-3,7-dioxa- bicyclo[3.3.0] octan-2-one. Acta Crystallographica Section E: Structure Reports Online, 57 (7), o566-o567. (doi:10.1107/S1600536801008170).

Record type: Article

Abstract

The title compound, C18H16O3, (I), was prepared in the course of studies towards the synthesis of furofuran ligands and was reported previously [Brown & Hinks (1998). Chem. Commun. pp. 1895-1896]. The compound is a a model system, where both oxygenated aromatic rings that are present in the natural products have been substituted by a simple phenyl group.

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Published date: 1 July 2001

Identifiers

Local EPrints ID: 19491
URI: http://eprints.soton.ac.uk/id/eprint/19491
PURE UUID: 621f2fb0-71b4-4a28-bcb1-694c697d25f8

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Date deposited: 16 Feb 2006
Last modified: 17 Jul 2017 16:31

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