(Q37510066)

20 August 2017

1 reference

title

Stereocontrolled synthesis of mannans and rhamnans (English)

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20 August 2017

3

David Crich

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20 August 2017

Feng Cai

1

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20 August 2017

Baolin Wu

series ordinal

2

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20 August 2017

publication date

1 January 2009

1 reference

Advances in Carbohydrate Chemistry and Biochemistry

20 August 2017

published in

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20 August 2017

volume

62

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20 August 2017

page(s)

251-309

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Tuning glycoside reactivity: New tool for efficient oligosaccharide synthesis

20 August 2017

cites work

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7 January 2021

A New Strategy for Oligosaccharide Assembly Exploiting Cyclohexane-1,2-diacetal Methodology: An Efficient Synthesis of a High Mannose Type Nonasaccharide

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7 January 2021

Synthesis of high-mannose type neoglycolipids: active targeting of liposomes to macrophages in gene therapy

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7 January 2021

Synthesis of a mannose heptasaccharide existing in baker's yeast, Saccharomyces cerevisiae X2180-1A wild-type strain

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https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis of the tetrasaccharide alpha-D-Glcp-(1-->3)-alpha-D-Manp-(1-->2)-alpha-D-Manp-(1-->2)-alpha-D-Manp recognized by calreticulin/calnexin

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https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthetic 3-O-methylmannose-containing polysaccharides (sMMPs): design and synthesis

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7 January 2021

Sequential one-pot glycosidations catalytically promoted: unprecedented strategy in oligosaccharide synthesis for the straightforward assemblage of the antitumor PI-88 pentasaccharide

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7 January 2021

De novo asymmetric bio- and chemocatalytic synthesis of saccharides - stereoselective formal O-glycoside bond formation using palladium catalysis

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7 January 2021

Stereoselective palladium-catalyzed O-glycosylation using glycals

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7 January 2021

De novo synthesis of oligosaccharides using a palladium-catalyzed glycosylation reaction

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Efficient synthesis of a 3,6-branched mannose hepta- and octasaccharide

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis of a mannose nonasaccharide existing in the exopolysaccharide of Cryphonectria parasitica

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Highly efficient and practical synthesis of 3,6-branched oligosaccharides.

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https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Total synthesis of phosphatidylinositol mannosides of Mycobacterium tuberculosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis and heparanase inhibitory activity of sulfated mannooligosaccharides related to the antiangiogenic agent PI-88.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis of a 6(V)-sulfated mannopentasaccharide analogue related to PI-88.

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https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

A strategy for ready preparation of glycolipids for multivalent presentation

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https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

An efficient approach towards the convergent synthesis of "fully-carbohydrate" mannodendrimers

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https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Regioselective strategies mediated by lanthanide triflates for efficient assembly of oligomannans

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Efficient synthesis of Man2, Man3, and Man5 oligosaccharides, using mannosyl iodide donors

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Syntheses of the octyl and tetradecyl glycosides of 3,6-di-O-alpha-D-mannopyranosyl-alpha-D-mannopyranose and of 3,4-di-O-alpha-D-mannopyranosyl-alpha-D-mannopyranose. A new way for 2,4-di-O-protection of mannopyranosides

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Highly stereoselective and iterative synthesis of alpha-(1-->4)-linked polysaccharides composed of 3-O-methyl-D-mannose

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Reactivity-based one-pot synthesis of oligomannoses: defining antigens recognized by 2G12, a broadly neutralizing anti-HIV-1 antibody

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis of branched Man5 oligosaccharides and an unusual stereochemical observation.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Syntheses of oligomannosides in solution and on a soluble polymer support: a comparison

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Cap and capture-release techniques applied to solid-phase synthesis of oligosaccharides

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Oligomannan synthesis using ionic liquid supported glycosylation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis of archaeal glycolipid adjuvants-what is the optimum number of sugars?

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

O-Glycosyl trichloroacetimidates bearing Fmoc as temporary hydroxy protecting group: a new access to solid-phase oligosaccharide synthesis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis of cyclo-L-rhamnopentaose

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Chemoselective Iterative Dehydrative Glycosylation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis of the antigenic tetrasaccharide side chain from the major glycoprotein of Bacillus anthracis exosporium

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis of the beta anomer of the spacer-equipped tetrasaccharide side chain of the major glycoprotein of the Bacillus anthracis exosporium

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis of the tetrasaccharide side chain of the major glycoprotein of the Bacillus anthracis exosporium

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Cyclohexane-1,2-diacetals(CDA): A New Protecting Group for Vicinal Diols in Carbohydrates

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Mammosides B and H1, new ionophoric resin-glycosides from the tuber of Merremia mammosa, an indonesian folk medicine.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis of the pentasaccharide repeating unit of the major O-antigen component from Pseudomonas syringae pv. ribicola NVPPB 1010.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis of glycosyl phosphates from 1,2-orthoesters and application to in situ glycosylation reactions.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Hydrophobically assisted switching phase synthesis: the flexible combination of solid-phase and solution-phase reactions employed for oligosaccharide preparation.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis of an L-rhamnose tetrasaccharide, the common and major structure of the repeating unit of the O-antigenic polysaccharide of a strain of Klebsiella pneumoniae and Pseudomonas holci

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Total synthesis of cleistetroside-2, partially acetylated dodecanyl tetrarhamnoside derivative isolated from Cleistopholis patens and Cleistopholis glauca

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

A concise synthesis of two isomeric pentasaccharides, the O repeat units from the lipopolysaccharides of P. syringae pv. porri NCPPB 3364T and NCPPB 3365.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis of an xylosylated rhamnose pentasaccharide, the repeating unit of the O-chain polysaccharide of the lipopolysaccharide of Xanthomonas campestris pv. begoniae GSPB 525.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis and antigenic analysis of the BclA glycoprotein oligosaccharide from the Bacillus anthracis exosporium

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Total synthesis of antigen bacillus anthracis tetrasaccharide--creation of an anthrax vaccine candidate

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis of a hexasaccharide fragment of group E streptococci polysaccharide and the tetrasaccharide repeating unit of E. coli O7:K98:H6.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Efficient synthesis of a heptasaccharide, the repeating unit of the O-chain lipopolysaccharide produced by Xanthomonas campestris strain 642.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis and conformational analysis of a pentasaccharide corresponding to the cell-wall polysaccharide of the Group A Streptococcus.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis of two linear PADRE conjugates bearing a deca- or pentadecasaccharide B epitope as potential synthetic vaccines against Shigella flexneri serotype 2a infection

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Blockwise approach to fragments of the O-specific polysaccharide of Shigella flexneri serotype 2a: convergent Synthesis of a decasaccharide representative of a dimer of the branched repeating unit

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Preparation of synthetic glycoconjugates as potential vaccines against Shigella flexneri serotype 2a disease

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis of beta-D-GlcpNAc-(1-->3)-alpha-L-Rhap-(1-->2)-[beta-L-Xylp-(1-->4)]-alpha-L-Rhap-(1-->3)-alpha-L-Rhap, the repeating unit of the O-antigen produced by Pseudomonas solanacearum ICMP 7942.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis and 2D-n.m.r. analysis of a pentasaccharide glycoside of the biological repeating units of Shigella flexneri variant Y polysaccharide and the preparation of a synthetic antigen

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

De novo asymmetric synthesis of the anthrax tetrasaccharide by a palladium-catalyzed glycosylation reaction

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

De novo asymmetric synthesis of anthrax tetrasaccharide and related tetrasaccharide

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

The chemical synthesis of beta-(1-->4)-linked D-mannobiose and D-mannotriose

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Preparation of disaccharides having a beta-D-mannopyranosyl group from N-phthaloyllactosamine derivatives by double or triple SN2 substitution

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

4,6-di-O-benzoyl-3-O-benzyl-alpha-D-arabino-hexo-pyranos-2-ulosyl bromide: a conveniently accessible glycosyl donor for the expedient construction of diantennary beta-D-mannosides branched at O-3 and O-6

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

The azidonitration of tri-O-acetyl-D-galactal

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

On the nitrile effect in L-rhamnopyranosylation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis of a beta1,2-mannopyranosyl tetrasaccharide found in the phosphomannan antigen of Candida albicans

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis of di- to hexasaccharide 1,2-linked beta-mannopyranan oligomers, a terminal S-linked tetrasaccharide congener and the corresponding BSA glycoconjugates

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis of glycoconjugate vaccines for Candida albicans using novel linker methodology

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Direct stereoselective synthesis of beta-thiomannosides

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis and biological studies of 35-deoxy amphotericin B methyl ester

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Beta-selective glycosylations with masked D-mycosamine precursors

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Direct synthesis of beta-mannans. A hexameric [-->3)-beta-D-Man-(1](3) subunit of the antigenic polysaccharides from Leptospira biflexa and the octameric (1-->2)-linked beta-D-mannan of the Candida albicans phospholipomannan. X-ray crystal structure

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Direct chemical synthesis of the beta-D-mannans: the beta-(1-->2) and beta-(1-->4) series

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

The unique solution structure and immunochemistry of the Candida albicans beta -1,2-mannopyranan cell wall antigens

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthetic analogues of beta-1,2 oligomannosides prevent intestinal colonization by the pathogenic yeast Candida albicans.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Regioselective reductive ring-opening of 4-methoxybenzylidene acetals of hexopyranosides. Access to a novel protecting-group strategy. Part 1

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

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://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Temperature-controlled regioselectivity in the reductive cleavage of p-methoxybenzylidene acetals

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Stereoselective direct glycosylation with anomeric hydroxy sugars by activation with phthalic anhydride and trifluoromethanesulfonic anhydride involving glycosyl phthalate intermediates

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

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://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Efficient installation of beta-mannosides using a dehydrative coupling strategy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Enhanced diastereoselectivity in beta-mannopyranosylation through the use of sterically minimal propargyl ether protecting groups

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Convergent synthesis of a beta-(1-->3)-mannohexaose

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

1-naphthylpropargyl ether group: a readily cleaved and sterically minimal protecting system for stereoselective glycosylation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis of beta-L-rhamnoside linked oligosaccharides of lipopolysaccharides from Shigella flexneri serotype 6

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Synthesis of a beta-(1-->3)-D-rhamnotetraose by a one-pot, multiple radical fragmentation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

On the regioselectivity of the Hanessian-Hullar reaction in 4,6-O-benzylidene protected galactopyranosides

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

Regiocontrol in the oxidative radical fragmentation of benzilidene acetals and its mechanistic implications

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

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://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

The synthesis of 2-acetamido-2-deoxy-4-O-beta-D-mannopyranosyl-D-glucose

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2318%2809%2900006-7

7 January 2021

10.1016/S0065-2318(09)00006-7

Identifiers

DOI

1 reference

20 August 2017

1 reference