β-Type glycosidic bond formation by palladium-catalyzed decarboxylative allylation.
about
A highly efficient dual catalysis approach for C-glycosylation: addition of (o-azaaryl)carboxaldehyde to glycals.Achmatowicz Reaction and its Application in the Syntheses of Bioactive Molecules.Divergent de novo synthesis of all eight stereoisomers of 2,3,6-trideoxyhexopyranosides and their oligomers.Reversing the stereoselectivity of a palladium-catalyzed O-glycosylation through an inner-sphere or outer-sphere pathway.One-pot synthesis of β-N-glycosyl imidazole analogues via a palladium-catalysed decarboxylative allylation.
P2860
β-Type glycosidic bond formation by palladium-catalyzed decarboxylative allylation.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
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2013年學術文章
@zh-hant
name
β-Type glycosidic bond formation by palladium-catalyzed decarboxylative allylation.
@en
β-Type glycosidic bond formation by palladium-catalyzed decarboxylative allylation.
@nl
type
label
β-Type glycosidic bond formation by palladium-catalyzed decarboxylative allylation.
@en
β-Type glycosidic bond formation by palladium-catalyzed decarboxylative allylation.
@nl
prefLabel
β-Type glycosidic bond formation by palladium-catalyzed decarboxylative allylation.
@en
β-Type glycosidic bond formation by palladium-catalyzed decarboxylative allylation.
@nl
P2093
P2860
P356
P1476
β-Type glycosidic bond formation by palladium-catalyzed decarboxylative allylation
@en
P2093
Kim Le Maihoang
Shaohua Xiang
Xue-Wei Liu
P2860
P304
14047-14051
P356
10.1002/CHEM.201303241
P407
P50
P577
2013-09-17T00:00:00Z