(Q41985350)

14 October 2017

Efficient glycosidation of a phenyl thiosialoside donor with diphenyl sulfoxide and triflic anhydride in dichloromethane (English)

1 reference

14 October 2017

1

David Crich

1 reference

14 October 2017

Wenju Li

2

1 reference

PMC publication ID

2615465

14 October 2017

language of work or name

English

0 references

publication date

1 March 2006

1 reference

14 October 2017

1 reference

14 October 2017

8

1 reference

14 October 2017

5

1 reference

14 October 2017

959-962

1 reference

Dehydrative sialylation with C2-hemiketal sialyl donors

14 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2615465

One-pot synthesis of sialo-containing glycosyl amino acids by use of an N-trichloroethoxycarbonyl-beta-thiophenyl sialoside

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2615465

Interhalogens (ICl/IBr) and AgOTf in thioglycoside activation; synthesis of bislactam analogues of ganglioside GD3.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2615465

1-Benzenesulfinyl piperidine/trifluoromethanesulfonic anhydride: a potent combination of shelf-stable reagents for the low-temperature conversion of thioglycosides to glycosyl triflates and for the formation of diverse glycosidic linkages

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2615465

A stereoselective approach for the synthesis of alpha-sialosides

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2615465

Recent Advances inO-Sialylation

18 August 2018

1 reference

12 December 2020

Chemoselective Iterative Dehydrative Glycosylation This research was supported by the National Institutes of Health (Grant no.: GM-58833), the Arnold and Mabel Beckman Foundation (BYI), Glaxo Wellcome Inc., and the Alfred P. Sloan Foundation. D.Y.G.

1 reference

12 December 2020

High-resolution 1H-NMR spectroscopy of free and glycosidically linked O-acetylated sialic acids

1 reference

12 December 2020

Stereoselective alpha-Sialylation with Sialyl Xanthate and Phenylsulfenyl Triflate as a Promotor

1 reference

12 December 2020

2-O-propargyl ethers: readily cleavable, minimally intrusive protecting groups for beta-mannosyl donors

1 reference

12 December 2020

N-trifluoroacetyl sialyl phosphite donors for the synthesis of alpha(2 --> 9) oligosialic acids

1 reference

12 December 2020

Efficient Sialylation with Phenyltrifluoroacetimidates as Leaving Groups

1 reference

12 December 2020

Identifiers

DOI

10.1021/OL060030S

1 reference

14 October 2017

1 reference

PMC publication ID

2615465

14 October 2017

PubMed publication ID

16494484

1 reference

PMC publication ID

2615465