(Q39215592)

10 September 2017

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

1 reference

10 September 2017

Hemali D Premathilake

series ordinal

1

1 reference

10 September 2017

Laurel K Mydock

series ordinal

2

1 reference

10 September 2017

Alexei V Demchenko

series ordinal

3

1 reference

10 September 2017

language of work or name

English

0 references

publication date

1 February 2010

1 reference

Journal of Organic Chemistry

10 September 2017

1 reference

10 September 2017

75

1 reference

10 September 2017

4

1 reference

10 September 2017

1095-1100

1 reference

Oligosaccharide synthesis: from conventional methods to modern expeditious strategies.

10 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827031

New principles for glycoside-bond formation

10 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827031

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

10 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827031

S-benzoxazolyl as a stable protecting moiety and a potent anomeric leaving group in oligosaccharide synthesis

10 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827031

Versatile synthesis and mechanism of activation of S-benzoxazolyl glycosides

10 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827031

Thioglycosides in sequential glycosylation strategies

10 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827031

Revisiting the armed-disarmed concept: the importance of anomeric configuration in the activation of S-benzoxazolyl glycosides

10 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827031

Unexpected orthogonality of S-benzoxazolyl and S-thiazolinyl glycosides: application to expeditious oligosaccharide assembly

10 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827031

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

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827031

Application of the superarmed glycosyl donor to chemoselective oligosaccharide synthesis.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827031

Thioglycosides as glycosyl donors in oligosaccharide synthesis.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827031

Stereoselective synthesis of allyl-C-mannosyl compounds: use of a temporary silicon connection in intramolecular allylation strategies with allylsilanes

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827031

The disarming effect of the 4,6-acetal group on glycoside reactivity: torsional or electronic?

21 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827031

Sulfide-mediated dehydrative glycosylation

21 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827031

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

21 August 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Synthesis of Oligosaccharide Structures from the Lipopolysaccharide of Moraxella catarrhalis

1 reference

12 December 2020

Development of an arming participating group for stereoselective glycosylation and chemoselective oligosaccharide synthesis

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1021/JO9021474

1 reference

10 September 2017

1 reference

10 September 2017

PubMed publication ID

20104917

1 reference