Chemical diversification of sialic acid glycosides by stereospecific, chemoselective deamination.

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Reductive Deamination by Benzyne for Deoxy Sugar Synthesis Through a Domino Reaction The isothiocyanato moiety: an ideal protecting group for the stereoselective synthesis of sialic acid glycosides and subsequent diversification.

P2860

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P2860

Chemical diversification of sialic acid glycosides by stereospecific, chemoselective deamination.

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http://www.wikidata.org/entity/Q42789515

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2013 nî lūn-bûn

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

@zh-hk

2013年論文

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2013年論文

@zh-tw

2013年论文

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2013年论文

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2013年论文

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name

Chemical diversification of si ...... c, chemoselective deamination.

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Chemical diversification of si ...... c, chemoselective deamination.

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type

Item

label

Chemical diversification of si ...... c, chemoselective deamination.

@en

Chemical diversification of si ...... c, chemoselective deamination.

@nl

prefLabel

Chemical diversification of si ...... c, chemoselective deamination.

@en

Chemical diversification of si ...... c, chemoselective deamination.

@nl

P1476

Chemical diversification of si ...... c, chemoselective deamination.

@en

P2093

Chandrasekhar Navuluri

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P2860

A Sialyltransferase Mutant with Decreased Donor Hydrolysis and Reduced Sialidase Activities for Directly Sialylating Lewis x

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Improving the antigenicity of sTn antigen by modification of its sialic acid residue for development of glycoconjugate cancer vaccines

C-5 modifications in N-acetyl-neuraminic acid: scope and limitations.

Stereoselective synthesis of alpha-keto-deoxy-D-glycero-D-galacto-nonulosonic acid glycosides by means of the 4,5-O-carbonate protecting group.

Protecting group-free glycoligation by the desulfurative rearrangement of allylic disulfides as a means of assembly of oligosaccharide mimetics.

alpha-selective sialylations at -78 degrees C in nitrile solvents with a 1-adamantanyl thiosialoside.

Highly alpha-selective sialyl phosphate donors for efficient preparation of natural sialosides.

O-sialylation with N-acetyl-5-n,4-o-carbonyl-protected thiosialoside donors in dichloromethane: facile and selective cleavage of the oxazolidinone ring.

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11339-11342

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scholarly article

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10.1002/ANIE.201303781

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English

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P478

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David Crich

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2013-09-13T00:00:00Z

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24038615

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3865865

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Chemical diversification of sialic acid glycosides by stereospecific, chemoselective deamination.

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P2860

P2860

Chemical diversification of sialic acid glycosides by stereospecific, chemoselective deamination.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932