Strict Stereocontrol by 2,4-O-Di-tert-butylsilylene Group on β-Glucuronylations-Reference-Cited by-同舟云学术

Strict Stereocontrol by 2,4-O-Di-tert-butylsilylene Group on β-Glucuronylations

Published:2012-04-03 Issue:8 Volume:14 Page:2102-2105
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Furukawa Takayuki¹,Hinou Hiroshi¹,Nishimura Shin-Ichiro¹

Affiliation:

1. Graduate School of Life Science and Frontier Research Center for Post-Genome Science and Technology, Hokkaido University, N21, W11, Kita-ku, Sapporo 001-0021, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol300634x

Reference41 articles.

1. Chemistry of 4,6-O-Benzylidene-d-glycopyranosyl Triflates: Contrasting Behavior between the Gluco and Manno Series

2. 4,6-O-Benzylidene-Directed β-Mannopyranosylation and α-Glucopyranosylation: The 2-Deoxy-2-fluoro and 3-Deoxy-3-fluoro Series of Donors and the Importance of the O2−C2−C3−O3 Interaction

3. β-Selective glucosylation in the absence of neighboring group participation: influence of the 3,4-O-bisacetal protecting system

4. On the Influence of the C2−O2 and C3−O3 Bonds in 4,6-O-Benzylidene-Directed β-Mannopyranosylation and α-Glucopyranosylation

5. Mechanism of a Chemical Glycosylation Reaction

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