cheminform abstract: gold(i)-catalyzed glycosylation with glycosyl ortho-alkynylbenzoates as donors:...

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ChemInform 2010, 41, issue 24 © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim www.cheminform.wiley-vch.de Carbohydrates U 0500 DOI: 10.1002/chin.201024183 Gold(I)-Catalyzed Glycosylation with Glycosyl ortho-Alkynylbenzoates as Donors: General Scope and Application in the Synthesis of a Cyclic Triterpene Saponin. — The new method can also be used for successful glycosylation of amides, α-selective glycosylation of 2-deoxy sugars, and β-selective sialylation. Moreover, this reaction is one of the key steps in the synthesis of a complex triterpene tetrasaccharide saponin. — (LI, Y.; YANG, X.; LIU, Y.; ZHU, C.; YANG, Y.; YU*, B.; Chem. Eur. J. 16 (2010) 6, 1871-1882; State Key Lab. Bioorg. Nat. Prod. Chem., Shanghai Inst. Org. Chem., Acad. Sin., Shanghai 200032, Peop. Rep. China; Eng.) — S. Adam 24- 183

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www.cheminform.wiley-vch.de

CarbohydratesU 0500 DOI: 10.1002/chin.201024183

Gold(I)-Catalyzed Glycosylation with Glycosyl ortho-Alkynylbenzoates as Donors: General Scope and Application in the Synthesis of a Cyclic Triterpene Saponin. — The new method can also be used for successful glycosylation of amides, α-selective glycosylation of 2-deoxy sugars, and β-selective sialylation. Moreover, this reaction is one of the key steps in the synthesis of a complex triterpene tetrasaccharide saponin. — (LI, Y.; YANG, X.; LIU, Y.; ZHU, C.; YANG, Y.; YU*, B.; Chem. Eur. J. 16 (2010) 6, 1871-1882; State Key Lab. Bioorg. Nat. Prod. Chem., Shanghai Inst. Org. Chem., Acad. Sin., Shanghai 200032, Peop. Rep. China; Eng.) — S. Adam

24- 183

ChemInform 2010, 41, issue 24 © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim

www.cheminform.wiley-vch.de

ChemInform 2010, 41, issue 24 © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim