(Q42739858)

English

Comparison of the armed/disarmed building blocks of the D-gluco and D-glucosamino series in the context of chemoselective oligosaccharide synthesis

scientific article published on July 2010

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

6 November 2017

Comparison of the armed/disarmed building blocks of the D-gluco and D-glucosamino series in the context of chemoselective oligosaccharide synthesis (English)

1 reference

Europe PubMed Central

PMC publication ID

6 November 2017

oligosaccharide

1 reference

based on heuristic

inferred from title

Alexei V. Demchenko

3

1 reference

Europe PubMed Central

PMC publication ID

6 November 2017

author name string

Teerada Kamkhachorn

1

1 reference

Europe PubMed Central

PMC publication ID

6 November 2017

Archana R Parameswar

2

1 reference

Europe PubMed Central

PMC publication ID

6 November 2017

language of work or name

0 references

publication date

1 July 2010

1 reference

Europe PubMed Central

PMC publication ID

6 November 2017

Organic Letters

1 reference

Europe PubMed Central

PMC publication ID

6 November 2017

12

1 reference

Europe PubMed Central

PMC publication ID

6 November 2017

13

1 reference

Europe PubMed Central

PMC publication ID

6 November 2017

3078-3081

1 reference

Europe PubMed Central

PMC publication ID

6 November 2017

Superarming common glycosyl donors by simple 2-O-benzoyl-3,4,6-tri-O-benzyl protection

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2895165

27 May 2018

Oligosaccharide synthesis: from conventional methods to modern expeditious strategies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2895165

27 May 2018

Superarming the S-benzoxazolyl glycosyl donors by simple 2-O-benzoyl-3,4,6-tri-O-benzyl protection

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2895165

27 May 2018

Going to extremes: "super" armed glycosyl donors in glycosylation chemistry

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2895165

27 May 2018

Chemoselective synthesis of oligosaccharides of 2-deoxy-2-aminosugars

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2895165

27 May 2018

Recent trends in the synthesis of O-glycosides of 2-amino-2-deoxysugars.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2895165

27 May 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2895165

27 May 2018

A Programmable One‐Pot Oligosaccharide Synthesis for Diversifying the Sugar Domains of Natural Products: A Case Study of Vancomycin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2895165

16 August 2018

Syntheses of anomerically phosphodiester-linked oligomers of the repeating units of the Haemophilus influenzae types c and f capsular polysaccharides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2895165

16 August 2018

One-pot synthesis of glucosamine oligosaccharides

1 reference

https://pubmed.ncbi.nlm.nih.gov/20527789

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Iterative one-pot synthesis of oligosaccharides

1 reference

https://pubmed.ncbi.nlm.nih.gov/20527789

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glycosylation with N-Troc-protected glycosyl donors

1 reference

https://pubmed.ncbi.nlm.nih.gov/20527789

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

N-trichloroethoxycarbonyl-glucosamine derivatives as glycosyl donors

1 reference

https://pubmed.ncbi.nlm.nih.gov/20527789

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Revisiting the armed-disarmed concept rationale: s-benzoxazolyl glycosides in chemoselective oligosaccharide synthesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20527789

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

S-thiazolinyl (STaz) glycosides as versatile building blocks for convergent selective, chemoselective, and orthogonal oligosaccharide synthesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20527789

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

"Super armed" glycosyl donors: conformational arming of thioglycosides by silylation

1 reference

https://pubmed.ncbi.nlm.nih.gov/20527789

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Conformationally armed glycosyl donors: reactivity quantification, new donors and one pot reactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/20527789

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/OL101089U

1 reference

Europe PubMed Central

PMC publication ID

6 November 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

6 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

6 November 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q42739858&oldid=1968619889"