The sn-diacylglycerols (DAGs) are important intermediates from a biological point of view. For this reason, the derivatization of DAGs with optically active protective groups represents an important strategy for their characterization. In this work a high-yielding enantiospecific synthesis of stable samples of DAGs as (S)-(1-naphthyl)-ethyl urethane derivatives is reported.

Enantiospecific synthesis of sn-1,2-, 2,3-, and 1,3-diacylglycerols as naphthylethylurethane derivatives

Rosati O.
Supervision
;
Blasi F.
Writing – Review & Editing
;
Montesano D.
Writing – Review & Editing
;
Persia D.
Formal Analysis
;
Marcotullio M. C.
Writing – Review & Editing
;
Monti B.
Writing – Review & Editing
;
Cossignani L.
Writing – Review & Editing
2019

Abstract

The sn-diacylglycerols (DAGs) are important intermediates from a biological point of view. For this reason, the derivatization of DAGs with optically active protective groups represents an important strategy for their characterization. In this work a high-yielding enantiospecific synthesis of stable samples of DAGs as (S)-(1-naphthyl)-ethyl urethane derivatives is reported.
2019
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11391/1456437
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