A novel and straightforward route to steroidal Z- and E-enol aldehydes is presented. Acid-catalysed treatment allows formal dismutation of corticosteroids, affording good yields of the related enol compounds which can be easily separated and purified.

A novel and straightforward route to steroidal Z- and E-enol aldehydes is presented. Acid-catalysed treatment allows formal dismutation of corticosteroids, affording good yields of the related enol compounds which can be easily separated and purified. (C) 2001 Elsevier Science Ltd. All rights reserved.

A facile approach to steroidal 20-hydroxy-17(20)-en-21-aldehydes: important intermediates in the biological 17-dehydroxylation of C-17 dihydroxyacetone steroids

DI GIOIA, Maria Luisa;LEGGIO, Antonella;LIGUORI, Angelo;NAPOLI, Anna Maria Carmela Natale V;SICILIANO, Carlo;SINDONA, Giovanni
2001-01-01

Abstract

A novel and straightforward route to steroidal Z- and E-enol aldehydes is presented. Acid-catalysed treatment allows formal dismutation of corticosteroids, affording good yields of the related enol compounds which can be easily separated and purified.
2001
A novel and straightforward route to steroidal Z- and E-enol aldehydes is presented. Acid-catalysed treatment allows formal dismutation of corticosteroids, affording good yields of the related enol compounds which can be easily separated and purified. (C) 2001 Elsevier Science Ltd. All rights reserved.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11770/136528
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