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Chemoselective alcoholysis of lactide mediated by a magnesium catalyst: an efficient route to alkyl lactyllactate.
Autorzy
Rok wydania
2011
Czasopismo
Numer woluminu
40
Strony
4042-4044
DOI
10.1039/c1dt10087d
Kolekcja
Język
Angielski
Typ publikacji
Artykuł
Alkyl-(S,S)-O-lactyllactate was prepared by chemoselective alcoholysis of lactide LA mediated by a magnesium catalyst. When ROH reacted with LA it yielded the ring-opened product R-(S,S)-O-lactyllactate exclusively, which remained intact as long as LA was present in the reaction mixture. Consumption of LA caused the reaction to proceed further giving R-(S)-lactate.
Adres publiczny
http://dx.doi.org/10.1039/c1dt10087d