A minimalist approach to stereoselective glycosylation with unprotected donors.

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Stereoselective oxidative glycosylation of anomeric nucleophiles with alcohols and carboxylic acids

P2860

Q58759663-9A3139F5-D1D1-413C-B73A-53C86E8E692C

P2860

A minimalist approach to stereoselective glycosylation with unprotected donors.

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http://www.wikidata.org/entity/Q42611963

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2017 nî lūn-bûn

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2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

@zh-cn

name

A minimalist approach to stereoselective glycosylation with unprotected donors.

@en

A minimalist approach to stereoselective glycosylation with unprotected donors.

@nl

type

Item

label

A minimalist approach to stereoselective glycosylation with unprotected donors.

@en

A minimalist approach to stereoselective glycosylation with unprotected donors.

@nl

prefLabel

A minimalist approach to stereoselective glycosylation with unprotected donors.

@en

A minimalist approach to stereoselective glycosylation with unprotected donors.

@nl

P1476

A minimalist approach to stereoselective glycosylation with unprotected donors

@en

P2093

Gábor Báti

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

Jing-Xi He

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

Mary B Chan-Park

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

Xue-Wei Liu

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

P2860

Studies on polynucleotides. 103. Total synthesis of the structural gene for an alanine transfer ribonucleic acid from yeast.

Erosion of stereochemical control with increasing nucleophilicity: O-glycosylation at the diffusion limit.

Synthesis and reactivity of 4'-deoxypentenosyl disaccharides.

Top-down chemoenzymatic approach to a high-mannose-type glycan library: synthesis of a common precursor and its enzymatic trimming.

A general strategy for the chemoenzymatic synthesis of asymmetrically branched N-glycans

Synthesis of biologically active N- and O-linked glycans with multisialylated poly-N-acetyllactosamine extensions using P. damsela α2-6 sialyltransferase.

Modular synthesis of N-glycans and arrays for the hetero-ligand binding analysis of HIV antibodies

Realizing the Promise of Chemical Glycobiology.

How the arming participating moieties can broaden the scope of chemoselective oligosaccharide synthesis by allowing the inverse armed-disarmed approach

Intramolecular aglycon delivery.

P2888

s41467-017-01073-7

P304

1146

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

P31

scholarly article

P356

10.1038/S41467-017-01073-7

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

P407

English

P433

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

P478

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

P50

Kim Le Mai Hoang

P577

2017-10-27T00:00:00Z

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

P698

29079775

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

P921

glycosylation

stereoselectivity

P932

5660076

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

A minimalist approach to stereoselective glycosylation with unprotected donors.

about

P2860

P2860

A minimalist approach to stereoselective glycosylation with unprotected donors.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932