In the presence of catalytic amounts of Cp*RuCl(cod), the cycloaddition of 1,6-diynes with various C-alkynylglycosides proceeded at ambient temperature to afford C-arylglycosides in 46-93% yields.
In the presence of catalytic amounts of Cp*RuCl(cod), the partially intramolecular cyclotrimerizations of various C-alkynylglycosides and C-diynylglycosides proceeded at ambient temperature to afford C-arylglycosides.
Carbohydrates U 0500Selective Synthesis of C-Arylglycosides via Cp*RuCl-Catalyzed Partially Intramolecular Cyclotrimerizations of C-Alkynylglycosides. -The method represents an efficient approach to diverse C-arylglycosides which are of biological interest. -(YAMAMOTO*, Y.; SAIGOKU, T.; NISHIYAMA, H.; OHGAI, T.; ITOH, K.; Org.
Synthesis of C-Arylglycosides via Ru(II)-Catalyzed [2 + 2 + 2] Cycloaddition. -In the presence of a Ru-catalyst, the cycloaddition of 1,6-diynes with various C-alkynylglycosides proceeds at ambient temperature to afford the title compounds, such as (III), (V), (VII), (IX) and (XI). -(YAMAMOTO*, Y.; SAIGOKU, T.; OHGAI, T.; NISHIYAMA, H.; ITOH, K.; Chem.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.