Selective anomeric acetylation of unprotected sugars in water.

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Strategies toward protecting group-free glycosylation through selective activation of the anomeric center.Protecting group free synthesis of glycosyl thiols from reducing sugars in water; application to the production of N-glycan glycoconjugates.

P2860

Q39427125-FCF6FC69-D78B-4939-BA1B-4AF570EAFD62 Q48223098-D8D59829-7EE2-4017-9AC7-66AD1C369E53

P2860

Selective anomeric acetylation of unprotected sugars in water.

Item

http://www.wikidata.org/entity/Q41886604

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Selective anomeric acetylation of unprotected sugars in water.

@en

type

Item

label

Selective anomeric acetylation of unprotected sugars in water.

@en

prefLabel

Selective anomeric acetylation of unprotected sugars in water.

@en

P1476

Selective anomeric acetylation of unprotected sugars in water

@en

P2093

David Lim

http://www.w3.org/2001/XMLSchema#string

P2860

Identification and molecular cloning of a novel glycoside hydrolase family of core 1 type O-glycan-specific endo-alpha-N-acetylgalactosaminidase from Bifidobacterium longum.

Molecular cloning, expression, and characterization of a novel endo-alpha-N-acetylgalactosaminidase from Enterococcus faecalis.

Regioselective modification of unprotected glycosides.

Advances in Enzymatic Glycoside Synthesis.

Ring-opening of aziridine-2-carboxamides with carbohydrate C1-O-nucleophiles. Stereoselective preparation of alpha- and beta-O-glycosyl serine conjugates.

C-H activation with elemental sulfur: synthesis of cyclic thioureas from formaldehyde aminals and S8.

1-O-Acetyl-beta-D-galactopyranose: a novel substrate for the transglycosylation reaction catalyzed by the beta-galactosidase from Penicillium sp.

One-step conversion of unprotected sugars to beta-glycosyl azides using 2-chloroimidazolinium salt in aqueous solution.

Efficient synthesis of sugar oxazolines from unprotected N-acetyl-2-amino sugars by using chloroformamidinium reagent in water.

Determination of proton affinities and acidity constants of sugars.

P304

1896-1900

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P31

scholarly article

P356

10.1039/C6SC04667C

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Antony J. Fairbanks

D Lim

P577

2016-11-17T00:00:00Z

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P698

28553480

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P932

5424810

http://www.w3.org/2001/XMLSchema#string

Selective anomeric acetylation of unprotected sugars in water.

about

P2860

P2860

Selective anomeric acetylation of unprotected sugars in water.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P932