(Q43669118)

25 November 2017

title

A highly efficient synthetic strategy for polymeric support synthesis of Le(x), Le(y), and H-type 2 oligosaccharides (English)

1 reference

25 November 2017

1 reference

Zhu T

1

1 reference

25 November 2017

Boons GJ

series ordinal

2

1 reference

25 November 2017

language of work or name

English

0 references

publication date

1 June 2001

1 reference

Chemistry—A European Journal

25 November 2017

published in

1 reference

25 November 2017

volume

7

1 reference

25 November 2017

issue

11

1 reference

25 November 2017

page(s)

2382-2389

1 reference

Combinatorial synthesis of carbohydrates

25 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010601%297%3A11%3C2382%3A%3AAID-CHEM23820%3E3.0.CO%3B2-2

Glycopeptide and Oligosaccharide Libraries

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010601%297%3A11%3C2382%3A%3AAID-CHEM23820%3E3.0.CO%3B2-2

A strategy for the solid-phase synthesis of oligosaccharides

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010601%297%3A11%3C2382%3A%3AAID-CHEM23820%3E3.0.CO%3B2-2

Parallel synthesis and screening of a solid phase carbohydrate library

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010601%297%3A11%3C2382%3A%3AAID-CHEM23820%3E3.0.CO%3B2-2

Organic Synthesis on Soluble Polymer Supports: Liquid-Phase Methodologies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010601%297%3A11%3C2382%3A%3AAID-CHEM23820%3E3.0.CO%3B2-2

From the Laboratory to the Clinic: A Retrospective on Fully Synthetic Carbohydrate-Based Anticancer Vaccines Frequently used abbreviations are listed in the appendix

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010601%297%3A11%3C2382%3A%3AAID-CHEM23820%3E3.0.CO%3B2-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010601%297%3A11%3C2382%3A%3AAID-CHEM23820%3E3.0.CO%3B2-2

Neue Methoden zur Glycosid- und Oligosaccharidsynthese – gibt es Alternativen zur Koenigs-Knorr-Methode?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010601%297%3A11%3C2382%3A%3AAID-CHEM23820%3E3.0.CO%3B2-2

Strategies in Oligosaccharide Synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010601%297%3A11%3C2382%3A%3AAID-CHEM23820%3E3.0.CO%3B2-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010601%297%3A11%3C2382%3A%3AAID-CHEM23820%3E3.0.CO%3B2-2

Polystyrylboronic acid as a reusable polymeric support for oligosaccharide synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010601%297%3A11%3C2382%3A%3AAID-CHEM23820%3E3.0.CO%3B2-2

Polymer-supported oligosaccharide synthesis by a loading–release–reloading strategy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010601%297%3A11%3C2382%3A%3AAID-CHEM23820%3E3.0.CO%3B2-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010601%297%3A11%3C2382%3A%3AAID-CHEM23820%3E3.0.CO%3B2-2

Solid-Phase Synthesis of Oligosaccharides: Construction of a Dodecasaccharide

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010601%297%3A11%3C2382%3A%3AAID-CHEM23820%3E3.0.CO%3B2-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010601%297%3A11%3C2382%3A%3AAID-CHEM23820%3E3.0.CO%3B2-2

Solid-phase oligosaccharide synthesis and related technologies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010601%297%3A11%3C2382%3A%3AAID-CHEM23820%3E3.0.CO%3B2-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010601%297%3A11%3C2382%3A%3AAID-CHEM23820%3E3.0.CO%3B2-2

The flouren-9-ylmethoxycarbonyl group for the protection of hydroxy-groups; its application in the synthesis of an octathymidylic acid fragment

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010601%297%3A11%3C2382%3A%3AAID-CHEM23820%3E3.0.CO%3B2-2

Levulinic esters. Alcohol protecting group applicable to some nucleosides

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010601%297%3A11%3C2382%3A%3AAID-CHEM23820%3E3.0.CO%3B2-2

A Two-Directional and Highly Convergent Approach for the Synthesis of the Tumor-Associated Antigen Globo-H

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010601%297%3A11%3C2382%3A%3AAID-CHEM23820%3E3.0.CO%3B2-2

Cancer-associated glycosphingolipid antigens: their structure, organization, and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3765%2820010601%297%3A11%3C2382%3A%3AAID-CHEM23820%3E3.0.CO%3B2-2

10.1002/1521-3765(20010601)7:11<2382::AID-CHEM23820>3.0.CO;2-2

21 January 2018

Identifiers

DOI

1 reference

25 November 2017

1 reference