An improved methodology to prepare (S)-2,3-O-cyclohexylideneglyceraldehyde is described. Starting from the commercially available (L)-cyclohexylidene protected ascorbic acid the enantiomerically pure aldehyde was synthesized in only two steps in 41% overall yield. [GRAPHICS]
An improved methodology for the synthesis of enantiomerically pure (S)-2,3-O-cyclohexylideneglyceraldehyde / M. Benaglia, M. Caporale, A. Puglisi. - In: ENANTIOMER. - ISSN 1024-2430. - 7:6(2002), pp. 383-385. [10.1080/10242430290015953]
An improved methodology for the synthesis of enantiomerically pure (S)-2,3-O-cyclohexylideneglyceraldehyde
M. BenagliaPrimo
;A. PuglisiUltimo
2002
Abstract
An improved methodology to prepare (S)-2,3-O-cyclohexylideneglyceraldehyde is described. Starting from the commercially available (L)-cyclohexylidene protected ascorbic acid the enantiomerically pure aldehyde was synthesized in only two steps in 41% overall yield. [GRAPHICS]
File in questo prodotto:
Non ci sono file associati a questo prodotto.
Pubblicazioni consigliate
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
