Application of the 4-trifluoromethylbenzenepropargyl ether group as an unhindered, electron deficient protecting group for stereoselective glycosylation.
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Mechanistic Investigations into the Application of Sulfoxides in Carbohydrate SynthesisThe 4-(tert-butyldiphenylsiloxy)-3-fluorobenzyl group: a new alcohol protecting group, fully orthogonal with the p-methoxybenzyl group and removable under desilylation conditions.Methodology development and physical organic chemistry: a powerful combination for the advancement of glycochemistry.Cation Clock Reactions for the Determination of Relative Reaction Kinetics in Glycosylation Reactions: Applications to Gluco- and Mannopyranosyl Sulfoxide and Trichloroacetimidate Type Donors.
P2860
Application of the 4-trifluoromethylbenzenepropargyl ether group as an unhindered, electron deficient protecting group for stereoselective glycosylation.
description
2008 nî lūn-bûn
@nan
2008年の論文
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2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
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2008年论文
@zh-cn
name
Application of the 4-trifluoro ...... stereoselective glycosylation.
@en
Application of the 4-trifluoro ...... stereoselective glycosylation.
@nl
type
label
Application of the 4-trifluoro ...... stereoselective glycosylation.
@en
Application of the 4-trifluoro ...... stereoselective glycosylation.
@nl
prefLabel
Application of the 4-trifluoro ...... stereoselective glycosylation.
@en
Application of the 4-trifluoro ...... stereoselective glycosylation.
@nl
P2860
P356
P1476
Application of the 4-trifluoro ...... stereoselective glycosylation.
@en
P2093
Maheswaran S Karatholuvhu
P2860
P304
P356
10.1021/JO7023398
P407
P50
P577
2008-06-05T00:00:00Z