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Tetrahedron: Asymmetry
Volume 4, Issue 6, June 1993, Pages 1325-1330
 
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doi:10.1016/S0957-4166(00)80243-8    
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Copyright © 1993 Published by Elsevier Science Ltd. All rights reserved.

Enantioselective epoxidation of styrene derivatives by chloroperoxidase catalysis

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Stefano Colonna, *a, Nicoletta Gaggeroa, Luigi Casellab, Giacomo Carreac and Piero Pastac

a Dipartimento di Chimica Organica e Industriale, Centro C.N.R., via Golgi 19, Milano, Italy

b Dipartimetno di Chimica Generale, Universita' di Pavia, via Taramelli 12, Pavia, Italy

c Istituto di Chimica degli Ormoni, C.N.R., via Mario Bianco 9, Milano, Italy


Received 1 February 1993. 
Available online 12 March 2001.

Abstract

Chloroperoxidase catalysed epoxidadon of styrene derivatives by t-BuOOH preferentially gives (R) oxides with ee values between 28 and 68%. The data support the view of oxygen delivery from the ferryl oxygen directly to the substrate.

Graphical Abstract


Stereochemistry Abstract



Image

Styrene oxide

C8H8O

E.e. = 49% (by chiral HPLC with Chiralcel OB column)

Source of chirality: Chloroperoxidase

Absolute configuration: R



Image

4-Chlostyrene oxide

C8H7C10

E.e. = 66% (by chiral HPLC with Chiralcel OB colunm)

Source of chirality: Chloroperoxidase

Absolute configuration: R



Image

3-Chlorostyrene oxide

C8H7ClO

E.e. = 62% (by chiral HPLC with Chiralcel OB column)

Source of chirality: Chloroperoxidase

Absolute configuration: R



Image

2-Chlorostyrene oxide

C8H7ClO

E.e. = 64% (by chiral HPLC with Chiralcel OB column)

Source of chirality: Chloroperoxidase

Absolute configuration: R



Image

4-Bromostyrene oxide

C8H7BrO

E.e. = 68% (by chiral HPLC with Chiralcel OB column)

Source of chirality: Chloroperoxidase

Absolute configuration: R



Image

4-Nitrostyrene oxide

C8H7NO3

E.e. = 28% (by chiral HPLC with Chiralcel OB column)

Source of chirality: Chloroperoxidase

Absolute configuration: R

Article Outline

• References


Tetrahedron: Asymmetry
Volume 4, Issue 6, June 1993, Pages 1325-1330
 
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