Monasson, Olivier et al. published their research in Synthesis in 2022 |CAS: 2873-29-2

The Article related to phosphorylation alkylphosphite glycal disaccharide monosaccharide preparation, monosaccharide disaccharide synthesis palladium catalyzed hirao cross coupling iodoglycal, Carbohydrates: Monosaccharides, Glycals and other aspects.Name: (2R,3S,4R)-2-(Acetoxymethyl)-3,4-dihydro-2H-pyran-3,4-diyl diacetate

On August 31, 2022, Monasson, Olivier; Malinowski, Maciej; Lubin-Germain, Nadege; Ferry, Angelique published an article.Name: (2R,3S,4R)-2-(Acetoxymethyl)-3,4-dihydro-2H-pyran-3,4-diyl diacetate The title of the article was Hirao Cross-Coupling Reaction as an Efficient Tool to Build Non-natural C2-Phosphonylated Sugars. And the article contained the following:

A range of C2-phosphonylated sugars have been accessed through a palladium-catalyzed Hirao cross-coupling on 2-iodoglycals using trialkylphosphites as phosphorylating reagents. The developed conditions led to the creation of an unnatural C-P bond on sugars and proved to be compatible with diversely protected glycals (acetyl-, benzyl-, PMB-protected) as well as with unprotected substrates. Several monosaccharides and one disaccharide have been synthesized by applying this methodol. Deprotection conditions are also described. The experimental process involved the reaction of (2R,3S,4R)-2-(Acetoxymethyl)-3,4-dihydro-2H-pyran-3,4-diyl diacetate(cas: 2873-29-2).Name: (2R,3S,4R)-2-(Acetoxymethyl)-3,4-dihydro-2H-pyran-3,4-diyl diacetate

The Article related to phosphorylation alkylphosphite glycal disaccharide monosaccharide preparation, monosaccharide disaccharide synthesis palladium catalyzed hirao cross coupling iodoglycal, Carbohydrates: Monosaccharides, Glycals and other aspects.Name: (2R,3S,4R)-2-(Acetoxymethyl)-3,4-dihydro-2H-pyran-3,4-diyl diacetate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics