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).
English
Settore BIO/10 - Biochimica
Articolo
Esperti anonimi
1987
11
2301
2303
Pubblicato
Periodico con rilevanza internazionale
Thomson Reuters Web of Knowledge
info:eu-repo/semantics/article
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.
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Prodotti della ricerca::01 - Articolo su periodico
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262
Article (author)
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P. FERRABOSCHI, R. CANEVOTTI, P. GRISENTI, E. SANTANIELLO
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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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