Preparation of L-vancosamine-related glycosyl donors

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Abstract

An improved practical synthesis of L-vancosamine-related glycosyl donors is described. The key steps include (1) stereoselective addition of methylcerium reagent to oximino ether and (2) stereoselective hydrogenation of exocyclic unsaturated glycoside in the presence of Wilkinson catalyst with C(5) inversion to give L-vancosamine derivatives. Three glycosyl donors were prepared, and their reactivities in the aryl C-glycoside formation were compared. Conversion of primary amine and azide to the corresponding N,N-dimethyl derivative is also described. © 2013 Japan Antibiotics Research Association All rights reserved.

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Kitamura, K., Shigeta, M., Maezawa, Y., Watanabe, Y., Hsu, D. S., Ando, Y., … Suzuki, K. (2013). Preparation of L-vancosamine-related glycosyl donors. Journal of Antibiotics, 66(3), 131–139. https://doi.org/10.1038/ja.2013.2

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