Ruthenium catalyzed synthesis of 2,3-unsaturated C-glycosides from glycals. 2015

Batthula Srinivas, and Thurpu Raghavender Reddy, and Sudhir Kashyap
D-207, Discovery Laboratory, Organic and Biomolecular Chemistry Division, CSIR-Indian Institute of Chemical Technology, Hyderabad 500 007, India.

A highly efficient and convenient C-glycosylation method was developed using ruthenium(III) chloride for the synthesis of 2,3-unsaturated C-glycosides. Various nucleophiles such as allyl trimethylsilane, triethylsilane, trimethylsilyl cyanide, trimethylsilyl azide and heterocycles such as thiophene and furan reacted smoothly with glycals in the presence of catalytic amount of ruthenium trichloride under mild reaction conditions.

UI MeSH Term Description Entries
D002384 Catalysis The facilitation of a chemical reaction by material (catalyst) that is not consumed by the reaction. Catalyses
D006027 Glycosides Any compound that contains a constituent sugar, in which the hydroxyl group attached to the first carbon is substituted by an alcoholic, phenolic, or other group. They are named specifically for the sugar contained, such as glucoside (glucose), pentoside (pentose), fructoside (fructose), etc. Upon hydrolysis, a sugar and nonsugar component (aglycone) are formed. (From Dorland, 28th ed; From Miall's Dictionary of Chemistry, 5th ed) Glycoside
D006031 Glycosylation The synthetic chemistry reaction or enzymatic reaction of adding carbohydrate or glycosyl groups. GLYCOSYLTRANSFERASES carry out the enzymatic glycosylation reactions. The spontaneous, non-enzymatic attachment of reducing sugars to free amino groups in proteins, lipids, or nucleic acids is called GLYCATION (see MAILLARD REACTION). Protein Glycosylation,Glycosylation, Protein
D012428 Ruthenium A hard, brittle, grayish-white rare earth metal with an atomic symbol Ru, atomic number 44, and atomic weight 101.07. It is used as a catalyst and hardener for PLATINUM and PALLADIUM.
D013237 Stereoisomerism The phenomenon whereby compounds whose molecules have the same number and kind of atoms and the same atomic arrangement, but differ in their spatial relationships. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 5th ed) Molecular Stereochemistry,Stereoisomers,Stereochemistry, Molecular,Stereoisomer

Related Publications

Batthula Srinivas, and Thurpu Raghavender Reddy, and Sudhir Kashyap
March 2005, Carbohydrate research,
Batthula Srinivas, and Thurpu Raghavender Reddy, and Sudhir Kashyap
March 2020, Organic & biomolecular chemistry,
Batthula Srinivas, and Thurpu Raghavender Reddy, and Sudhir Kashyap
January 2019, Beilstein journal of organic chemistry,
Batthula Srinivas, and Thurpu Raghavender Reddy, and Sudhir Kashyap
December 2023, The Journal of organic chemistry,
Batthula Srinivas, and Thurpu Raghavender Reddy, and Sudhir Kashyap
May 2023, Angewandte Chemie (International ed. in English),
Batthula Srinivas, and Thurpu Raghavender Reddy, and Sudhir Kashyap
May 2002, Organic letters,
Batthula Srinivas, and Thurpu Raghavender Reddy, and Sudhir Kashyap
October 2007, Carbohydrate research,
Batthula Srinivas, and Thurpu Raghavender Reddy, and Sudhir Kashyap
March 2024, Organic letters,
Batthula Srinivas, and Thurpu Raghavender Reddy, and Sudhir Kashyap
July 2018, Organic & biomolecular chemistry,
Batthula Srinivas, and Thurpu Raghavender Reddy, and Sudhir Kashyap
April 2024, Organic letters,
Copied contents to your clipboard!