(Q41774744)

English

Stereocontrolled synthesis of the D- and L-glycero-beta-D-manno-heptopyranosides and their 6-deoxy analogues. Synthesis of methyl alpha-l-rhamno-pyranosyl-(1-->3)-D-glycero-beta-D-manno-heptopyranosyl- (1-->3)-6-deoxy-glycero-beta-D-manno-heptopyran

scientific article published on June 2006

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

Stereocontrolled synthesis of the D- and L-glycero-beta-D-manno-heptopyranosides and their 6-deoxy analogues. Synthesis of methyl alpha-l-rhamno-pyranosyl-(1-->3)-D-glycero-beta-D-manno-heptopyranosyl- (1-->3)-6-deoxy-glycero-beta-D-manno-heptopyran (English)

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

1

object named as

David Crich

1 reference

Europe PubMed Central

9 October 2017

PMC publication ID

author name string

Abhisek Banerjee

2

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

language of work or name

0 references

publication date

1 June 2006

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

Journal of the American Chemical Society

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

128

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

24

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

8078-8086

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

Synthesis and conformational analysis of 6-C-methyl-substituted 2-acetamido-2-deoxy-beta-D-glucopyranosyl mono- and disaccharides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2617734

6 June 2018

The mechanism of the reaction catalyzed by ADP-beta-L-glycero-D-manno-heptose 6-epimerase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2617734

6 June 2018

Lipopolysaccharide endotoxins

1 reference

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6 June 2018

Core oligosaccharides of Plesiomonas shigelloides O54:H2 (strain CNCTC 113/92): structural and serological analysis of the lipopolysaccharide core region, the O-antigen biological repeating unit, and the linkage between them

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2617734

6 June 2018

Structural studies of the O-specific polysaccharide from Plesiomonas shigelloides strain CNCTC 113/92.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2617734

6 June 2018

Synthesis of a hexasaccharide corresponding to part of the heptose-hexose region of the Salmonella Ra core, and a penta- and a tetra-saccharide that compose parts of this structure.

1 reference

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6 June 2018

The design and synthesis of antibody binding site probes: three pentasaccharide analogues of the Brucella A antigen prepared by activation in situ of thioglycosides with bromine

1 reference

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6 June 2018

4,6-O-[1-cyano-2-(2-iodophenyl)ethylidene] acetals. improved second-generation acetals for the stereoselective formation of beta-D-mannopyranosides and regioselective reductive radical fragmentation to beta-D-rhamnopyranosides. scope and limitations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2617734

18 August 2018

A short synthesis of D-glycero-D-manno-heptose 7-phosphate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2617734

18 August 2018

Direct chemical synthesis of the beta-mannans: linear and block syntheses of the alternating beta-(1-->3)-beta-(1-->4)-mannan common to Rhodotorula glutinis, Rhodotorula mucilaginosa, and Leptospira biflexa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2617734

18 August 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2617734

18 August 2018

A novel strategy towards the synthesis of orthogonally functionalised 4-aminoglycosides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2617734

18 August 2018

Efficient chemical synthesis of both anomers of ADP L-glycero- and D-glycero-D-manno-heptopyranose

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2617734

18 August 2018

The 3,4-O-Carbonate Protecting Group as a β-Directing Group in Rhamnopyranosylation in Both Homogeneous and Heterogeneous Glycosylations As Compared to the Chameleon-like 2,3-O-Carbonates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2617734

18 August 2018

Deoxygenation of carbohydrates by thiol-catalysed radical-chain redox rearrangement of the derived benzylidene acetals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2617734

18 August 2018

A simple method for preparation of D-rhamnose

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2617734

18 August 2018

Total synthesis of desferrisalmycin B.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2617734

18 August 2018

Synthesis of the Salmonella type E(1) core trisaccharide as a probe for the generality of 1-(benzenesulfinyl)piperidine/triflic anhydride combination for glycosidic bond formation from thioglycosides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2617734

18 August 2018

Metal trifluoromethanesulfonate-catalyzed regioselective borane-reductive ring opening of benzylidene acetals: a concise synthesis of 1,4-dideoxy-1,4-imino-L-xylitol.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2617734

18 August 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2617734

18 August 2018

Template-directed C-H insertion: synthesis of the dioxabicyclo[3.2.1]octane core of the zaragozic acids.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2617734

18 August 2018

A convenient route to higher sugars by two-carbon chain elongation using Wittig/dihydroxylation reactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2617734

18 August 2018

The preparation of D-rhamnose from methyl alpha-d-mannopyranoside

1 reference

https://pubmed.ncbi.nlm.nih.gov/16771524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Practical Method for the Removal of Organotin Residues from Reaction Mixtures

1 reference

https://pubmed.ncbi.nlm.nih.gov/16771524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Benzylidene acetal fragmentation route to 6-deoxy sugars: direct reductive cleavage in the presence of ether protecting groups, permitting the efficient, highly stereocontrolled synthesis of beta-D-rhamnosides from D-mannosyl glycosyl donors. Total

1 reference

https://pubmed.ncbi.nlm.nih.gov/16771524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ph2SO/Tf2O: a Powerful Promotor System in Chemoselective Glycosylations Using Thioglycosides

1 reference

https://pubmed.ncbi.nlm.nih.gov/16771524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Efficient chemoenzymatic synthesis of ADP-D-glycero-beta-D-manno-heptose and a mechanistic study of ADP-L-glycero-D-manno-heptose 6-epimerase

1 reference

https://pubmed.ncbi.nlm.nih.gov/16771524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Direct synthesis of the beta-l-rhamnopyranosides

1 reference

https://pubmed.ncbi.nlm.nih.gov/16771524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Facile bromination by N-bromosuccinimide of benzylidene acetals of carbohydrates. Application to the synthesis of 2,6-imino carbohydrates (substituted 2,5-oxazabicyclo[2.2.2] octanes)

1 reference

https://pubmed.ncbi.nlm.nih.gov/16771524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 4,6-O-[alpha-(2-(2- iodophenyl)ethylthiocarbonyl)benzylidene] protecting group: stereoselective glycosylation, reductive radical fragmentation, and synthesis of beta-D-rhamnopyranosides and other deoxy sugars

1 reference

https://pubmed.ncbi.nlm.nih.gov/16771524

12 December 2020

based on heuristic

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Total synthesis of the boron-containing ion carrier antibiotic macrodiolide tartrolon B

1 reference

https://pubmed.ncbi.nlm.nih.gov/16771524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthesis and stereoselective glycosylation of D- and L-glycero-beta-D-manno-heptopyranoses

1 reference

https://pubmed.ncbi.nlm.nih.gov/16771524

12 December 2020

based on heuristic

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Synthesis of L-glycero-D-manno-heptopyranose-containing oligosaccharide structures found in lipopolysaccharides from Haemophilus influenzae

1 reference

https://pubmed.ncbi.nlm.nih.gov/16771524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/JA061594U

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

release_2kbqusnj5rhlrbuvsqbtztm4fm

1 reference

https://api.fatcat.wiki/v0/release/2kbqusnj5rhlrbuvsqbtztm4fm

24 November 2022

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PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

ResearchGate publication ID

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