(Q34489520)

2 August 2017

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title

New approaches to the chemical synthesis of bioactive oligosaccharides (English)

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2 August 2017

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Bartolozzi A

1

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PubMed ID

11785760

2 August 2017

Seeberger PH

series ordinal

2

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2 August 2017

1 October 2001

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Current Opinion in Structural Biology

2 August 2017

1 reference

2 August 2017

11

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2 August 2017

587-592

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2 August 2017

5

1 reference

The 2-naphthylmethyl (NAP) group in carbohydrate synthesis: first total synthesis of the GlyCAM-1 oligosaccharide structures

2 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Total synthesis of sialylated and sulfated oligosaccharide chains from respiratory mucins

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

A General and Highly Efficient Solid Phase Synthesis of Oligosaccharides. Total Synthesis of a Heptasaccharide Phytoalexin Elicitor (HPE)

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

O-Glycosyl trichloroacetimidates bearing Fmoc as temporary hydroxy protecting group: a new access to solid-phase oligosaccharide synthesis

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

A new set of orthogonal-protecting groups for oligosaccharide synthesis on a polymeric support

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Use of fluorobenzoyl protective groups in synthesis of glycopeptides: beta-elimination of O-linked carbohydrates is suppressed

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Synthesis of glycosyl-1-phosphates via dehydrative glycosylation

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Synthesis and use of glycosyl phosphates as glycosyl donors

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Formation of beta-glucosamine and beta-mannose linkages using glycosyl phosphates

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Synthesis of C-aryl and C-alkyl glycosides using glycosyl phosphates

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Synthesis and growth inhibitory properties of glucosamine-derived glycerolipids

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Reductive Samariation of Anomeric 2-Pyridyl Sulfones with Catalytic Nickel: An Unexpected Improvement in the Synthesis of 1,2-trans-Diequatorial C-Glycosyl Compounds

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Glycosyl sulfonylcarbamates: new glycosyl donors with tunable reactivity.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

A Direct and Efficientα-Selective Glycosylation Protocol for the Kedarcidin Sugar,L-Mycarose: AgPF6 as a Remarkable Activator of 2-Deoxythioglycosides

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Stereoselective synthesis of 2-hydroxy-alpha-mannopyranosides from glucal donors

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Total synthesis of everninomicin 13,384-1--Part 1: retrosynthetic analysis and synthesis of the A1B(A)C fragment.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Total synthesis of everninomicin 13,384-1--Part 2: synthesis of the FGHA2 fragment

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Total synthesis of everninomicin 13,384-1--Part 3: synthesis of the DE fragment and completion of the total synthesis.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Total synthesis of everninomicin 13,384-1--Part 4: explorations of methodology; stereocontrolled synthesis of 1,1'-disaccharides, 1,2-seleno migrations in carbohydrates, and solution- and solid-phase synthesis of 2-deoxy glycosides and orthoesters

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Toward Fully Synthetic Homogeneous Glycoproteins: A High Mannose Core Containing Glycopeptide Carrying Full H-Type 2 Human Blood Group Specificity This work was supported by the National Institutes of Health (Grant nos.: HL-25848 and CA-28824 (to S.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Total syntheses of tumor-related antigens N3: probing the feasibility limits of the glycal assembly method

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Pursuit of optimal carbohydrate-based anticancer vaccines: preparation of a multiantigenic unimolecular glycopeptide containing the Tn, MBr1, and Lewis(y) antigens

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Synthesis of phosphorylated and sulfated glycosyl serines in the linkage region of the glycosaminoglycans

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Synthesis of Conformationally Locked Carbohydrates: A Skew-Boat Conformation of L-Iduronic Acid Governs the Antithrombotic Activity of Heparin

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

First Total Synthesis of the Re-Type Lipopolysaccharide This work was supported by the Research for the Future Program (No. 97L00502) from the Japan Society for the Promotion of Science. H.Y. is grateful for a JSPS Research Fellowship for Young Scie

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Polymer-supported and chemoenzymatic synthesis of the Neisseria meningitidis pentasaccharide: a methodological comparison

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

A highly convergent synthesis of a complex oligosaccharide derived from group B type III Streptococcus

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

An efficient access to protected disialylated glycohexaosyl threonine present on the leukosialin of activated T-lymphocytes

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Gene synthesis machines: DNA chemistry and its uses

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Solid Phase Peptide Synthesis. I. The Synthesis of a Tetrapeptide

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Solid-phase oligosaccharide synthesis: preparation of complex structures using a novel linker and different glycosylating agents

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Quantitative Monitoring of Solid-Phase Synthesis Using Gated Decoupling 13 C NMR Spectroscopy with a 13 C-Enriched Protecting Group and an Internal Standard in the Synthesis of Sialyl LewisX Tetrasaccharide

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Monitoring solid-phase glycoside synthesis with (19)F NMR spectroscopy

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Tag-reporter strategy for facile oligosaccharide synthesis on polymer support.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

A Novel and Efficient Synthesis of a Dimeric LexOligosaccharide on Polymeric Support

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Automated solid-phase synthesis of oligosaccharides

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Anomeric reactivity-based one-pot oligosaccharide synthesis: a rapid route to oligosaccharide libraries

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

Synthesis of the Globo H Hexasaccharide Using the Programmable Reactivity-Based One-Pot Strategy This research was supported by the National Institutes of Health. F.B. thanks the Deutsche Forschungsgemeinschaft for a fellowship

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2800%2900252-9

7 January 2021

10.1016/S0959-440X(00)00252-9

Identifiers

DOI

1 reference

2 August 2017

1 reference

PubMed ID

11785760