By selective ozonolysis of the diene (5), a new synthesis of (R,S)-mevalonolactone (1a) has been developed, which can be adapted to other compounds related to (1a). This has been exemplified by the synthesis of the monodeuteriated triol (4d) and dideuteriated mevalonolactone (1d).

A NEW FLEXIBLE SYNTHESIS OF (R,S)-MEVALONOLACTONE / P. FERRABOSCHI, R. CANEVOTTI, P. GRISENTI, E. SANTANIELLO. - In: JOURNAL OF THE CHEMICAL SOCIETY. PERKIN TRANSACTIONS. I. - ISSN 0300-922X. - :11(1987), pp. 2301-2303.

A NEW FLEXIBLE SYNTHESIS OF (R,S)-MEVALONOLACTONE

P. FERRABOSCHI
Primo
;
E. SANTANIELLO
Ultimo
1987

Abstract

By selective ozonolysis of the diene (5), a new synthesis of (R,S)-mevalonolactone (1a) has been developed, which can be adapted to other compounds related to (1a). This has been exemplified by the synthesis of the monodeuteriated triol (4d) and dideuteriated mevalonolactone (1d).
Settore BIO/10 - Biochimica
1987
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/181005
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