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Synthesis of pentaarabinofuranosyl structure motif A of Mycobacterium tuberculosis

https://doi.org/10.1039/a707796c
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1016/0008-6215(87)80065-4openalex-snapshot
Demonstration that the galactosyl and arabinosyl residues in the cell-wall arabinogalactan of Mycobacterium leprae and Myobacterium tuberculosis are furanoid
inferredcites →https://doi.org/10.1016/0008-6215(91)80132-7openalex-snapshot
Convenient syntheses of 2,3,5-tri-O-benzyl-arabino- and −ribofuranoses via their allyl glycosides
inferredcites →https://doi.org/10.1016/0008-6215(92)84166-popenalex-snapshot
Preparation of new acylated derivatives of l -arabino-furanose and 2-deoxy- l - erythro -pentofuranose as precursors for the synthesis of l -pentofuranosyl nucleosides
inferredcites →https://doi.org/10.1016/0008-6215(93)84227-wopenalex-snapshot
Synthesis of methyl 3-O-(2-O-methyl-α-l-fucopyranosyl)-α-l-rhamnopyranoside, methyl 3-O-α-l-rhamnopyranosyl-α-d-glucopyranoside, and methyl 3-O-[3-O-(2-O-methyl-α-l-fucopyranosyl)-α-l-rhamnopyranosyl]-α-l-rhamnopyranoside: di- and tri-saccharide segments of a lipo-oligosaccharide (LOS-1) of…
inferredcites →https://doi.org/10.1016/0040-4039(91)80786-6openalex-snapshot
A stereoconvergent synthesis of the oligosaccharide segment of glyco- peptidolipid antigen of mycobacterium avium serotype 4 : a dominant serovariant observed in patients with acquired immune deficiency syndrome
inferredcites →https://doi.org/10.1016/s0021-9258(19)39211-7openalex-snapshot
Predominant structural features of the cell wall arabinogalactan of Mycobacterium tuberculosis as revealed through characterization of oligoglycosyl alditol fragments by gas chromatography/mass spectrometry and by 1H and 13C NMR analyses.
inferredcites →https://doi.org/10.1016/s0040-4020(01)80018-1openalex-snapshot
Synthesis of methyl 3--[3--(2,3,4-tri--methyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranosyl]-α-L-rhamnopyranoside : The outer trisaccharide unit of a unique glycopeptidolipid
inferredcites →https://doi.org/10.1016/s0040-4020(01)86571-6openalex-snapshot
Stereoselective synthesis of α-linked saccharides by use of per O-benzylated 2-pyridyl 1-thio hexopyranosides as glycosyl donors and methyl iodide as an activator
inferredcites →https://doi.org/10.1016/s0040-4020(01)88483-0openalex-snapshot
Synthesis of the glycopeptide - O-(3,4-di-O-methyl-2-O-[3,4-di-O-methyl-α-L-rhamnopyranosyl]-α-L-rhamnopyranosyl)-L-alanilol: An unusual part structure in the glycopeptidolipid of
inferredcites →https://doi.org/10.1016/s0040-4020(97)00532-2openalex-snapshot
Synthesis of the unique terminal branched tetrasaccharide of Mycobacterium gordonae strain 990
inferredcites →https://doi.org/10.1016/s0040-4039(00)61250-9openalex-snapshot
Synthesis of a new serine containing glycotetrapeptide from glycopeptidolipid : An unusual structural variant in mycobacterium genus
inferredcites →https://doi.org/10.1021/bi00013a015openalex-snapshot
A new interpretation of the structure of the mycolyl-arabinogalactan complex of Mycobacterium tuberculosis as revealed through characterization of oligoglycosylalditol fragments by fast-atom bombardment mass spectrometry and 1H nuclear magnetic resonance spectroscopy
inferredcites →https://doi.org/10.1080/07328309108543923openalex-snapshot
Communication: Synthesis of Me α-L-Rhap-(1↠3)-2-O-Me-α-L-Rhap And Me 2,3,4-Tri-O-Me-α-L-Fucp-(1↠3)-α-L-Rhap-(1↠3)-2-O-Me-α-L-Rhap : Oligosaccha-Ride Segments of Phenolic Glycolipids inMycobacterium Bovis BcgandTuberculosis Strain Canetti
inferredcites →https://doi.org/10.1139/v65-296openalex-snapshot
THE SYNTHESIS OF β- D -GLUCOPYRANOSYL 2-DEOXY-α- D -ARABINO-HEXOPYRANOSIDE

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4854112openalex-extracted
Total Synthesis of the Hexasaccharide Arabinan Domain of Mycobacterial Arabinogalactan
inferred← citeshttps://doi.org/10.1002/9781119006435.ch14openalex-snapshot
SYNTHESIS OF BACTERIAL CELL ENVELOPE COMPONENTS
inferred← citeshttps://doi.org/10.1002/9783527621644.ch4bopenalex-snapshot
Glycoside Synthesis from 1‐Sulfur/Selenium‐Substituted Derivatives: Sections 4.3 and 4.4
inferred← citeshttps://doi.org/10.1002/ajoc.202000107openalex-snapshot
Intrinsic Issues in the Assembly of 1,2‐Linked Oligosaccharides
inferred← citeshttps://doi.org/10.1002/ange.202502837openalex-snapshot
Synthesis of Glycolipid Library Reminiscent of Mycobacterial Cell Wall Motif A and Its Significance by Microscopy
inferred← citeshttps://doi.org/10.1002/anie.202502837openalex-snapshot
Synthesis of Glycolipid Library Reminiscent of Mycobacterial Cell Wall Motif A and Its Significance by Microscopy
inferred← citeshttps://doi.org/10.1002/chem.201704009openalex-snapshot
A Versatile Synthesis of Pentacosafuranoside Subunit Reminiscent of Mycobacterial Arabinogalactan Employing One Strategic Glycosidation Protocol
inferred← citeshttps://doi.org/10.1002/chin.199830236openalex-snapshot
ChemInform Abstract: Synthesis of Pentaarabinofuranosyl Structure Motif A of Mycobacterium tuberculosis.
inferred← citeshttps://doi.org/10.1002/ejoc.200300303openalex-snapshot
Synthesis of Oligoarabinofuranosides from the Mycobacterial Cell Wall
inferred← citeshttps://doi.org/10.1002/ejoc.201700712openalex-snapshot
Expedient Synthesis of a Linear Nonadecaarabinofuranoside of the Mycobacterium tuberculosis Cellular Envelope
inferred← citeshttps://doi.org/10.1002/ejoc.202201110openalex-snapshot
Five Triisopropylsilyl Substituents in Ara‐β‐(1→2)‐Ara Disaccharide Glycosyl Donor Make Unselective Glycosylation Reaction Stereoselective
inferred← citeshttps://doi.org/10.1002/tcr.20138openalex-snapshot
Lactonization‐mediated glycosylations and their application to oligosaccharide synthesis
inferred← citeshttps://doi.org/10.1007/978-3-540-30429-6_13openalex-snapshot
O-Glycosyl Donors
inferred← citeshttps://doi.org/10.1007/978-3-540-30429-6_40openalex-snapshot
Synthesis of Glycolipids
inferred← citeshttps://doi.org/10.1007/978-3-642-56874-9_48openalex-snapshot
Mycobacterial Cell Wall Components
inferred← citeshttps://doi.org/10.1007/s11172-022-3371-zopenalex-snapshot
The use of silyl groups in the synthesis of arabinofuranosides
inferred← citeshttps://doi.org/10.1007/s11172-024-4260-4openalex-snapshot
Synthesis of hexaarabinofuranoside bearing the 4-(3-azidopropoxy)phenyl aglycone related to the terminal fragment of polysaccharides of mycobacteria
inferred← citeshttps://doi.org/10.1016/j.bmc.2005.12.037openalex-snapshot
Synthesis and TNF-α inducing activities of mycoloyl-arabinan motif of mycobacterial cell wall components
inferred← citeshttps://doi.org/10.1016/j.carres.2005.01.008openalex-snapshot
Stereoselective synthesis of a ketohexofuranose from an aldohexopyranose by a [6+1−1] strategy
inferred← citeshttps://doi.org/10.1016/j.carres.2008.09.006openalex-snapshot
Synthesis of β-d-arabinofuranosides: stereochemical differentiation between d- and l-enantiomers
inferred← citeshttps://doi.org/10.1016/j.carres.2012.05.021openalex-snapshot
Synthesis of branched arabinofuranose pentasaccharide fragment of mycobacterial arabinans as 2-azidoethyl glycoside
inferred← citeshttps://doi.org/10.1016/j.carres.2014.05.017openalex-snapshot
The use of O-trifluoroacetyl protection and profound influence of the nature of glycosyl acceptor in benzyl-free arabinofuranosylation
inferred← citeshttps://doi.org/10.1016/j.carres.2016.05.009openalex-snapshot
Rapid synthesis of linear homologous oligoarabinofuranosides related to mycobacterial lipoarabinomannan and a neoglycoconjugate thereof
inferred← citeshttps://doi.org/10.1016/j.carres.2016.11.006openalex-snapshot
Preparation of the tri-arabino di-mycolate fragment of mycobacterial arabinogalactan from defined synthetic mycolic acids
inferred← citeshttps://doi.org/10.1016/j.carres.2016.11.009openalex-snapshot
Bimodal concentration-dependent reactivity pattern of a glycosyl donor: Is the solution structure involved?
inferred← citeshttps://doi.org/10.1016/j.carres.2024.109141openalex-snapshot
Unusual triflic acid-promoted oligomerization of arabinofuranosides during glycosylation
inferred← citeshttps://doi.org/10.1016/j.carres.2024.109204openalex-snapshot
Total synthesis of the hexasaccharide arabinan domain of mycobacterial arabinogalactan
inferred← citeshttps://doi.org/10.1016/j.carres.2024.109252openalex-snapshot
Stereocontrolled 1,2-trans-arabinofuranosylation in the absence of 2-O-acyl group in glycosyl donor
inferred← citeshttps://doi.org/10.1016/j.carres.2025.109622openalex-snapshot
Application of Ara-β-(1 → 2)-Ara diarabinofuranosides with O-TBDPS protective groups in the synthesis of the tetra- and dodecaarabinofuranosides – fragments of mycobacterial polysaccharides
inferred← citeshttps://doi.org/10.1016/j.chemphyslip.2019.01.002openalex-snapshot
The synthesis of mycobacterial dimycoloyl diarabinoglycerol based on defined synthetic mycolic acids
inferred← citeshttps://doi.org/10.1016/s0008-6215(00)00159-2openalex-snapshot
An efficient and concise regioselective synthesis of α-(1→5)-linked l-arabinofuranosyl oligosaccharides
inferred← citeshttps://doi.org/10.1016/s0008-6215(99)00078-6openalex-snapshot
Synthesis of methyl β-d-arabinofuranoside 5-[1d (and l)-myo-inositol 1-phosphate], the capping motif of the lipoarabinomannan of Mycobacteriumsmegmatis
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)01273-9openalex-snapshot
A comprehensive glycosylation system for the elaboration of oligoarabinofuranosides
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)01327-2openalex-snapshot
Synthesis of d-arabinofuranosides using propane-1,3-diyl phosphate as the anomeric leaving group
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)01760-4openalex-snapshot
First synthesis of methyl α-C-d-arabinofuranosyl-(1→5)-α-d-arabinofuranoside: the C-disaccharide segment of motif C of Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.1016/s1367-5931(01)00265-4openalex-snapshot
Chemistry and biology of arabinofuranosyl- and galactofuranosyl-containing polysaccharides
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00964openalex-snapshot
Influence of Steric Crowding on Diastereoselective Arabinofuranosylations
inferred← citeshttps://doi.org/10.1021/acs.joc.5b01686openalex-snapshot
Synthetic and Immunological Studies of Mycobacterial Lipoarabinomannan Oligosaccharides and Their Protein Conjugates
inferred← citeshttps://doi.org/10.1021/acs.joc.6b01723openalex-snapshot
Phthalic Anhydride-Mediated Direct Glycosylation of Anomeric Hydroxy Arabinofuranose: Synthesis of Repeating Oligoarabinofuranoside and Tetradecasaccharide Arabinan Motif of Mycobacterial Cell Wall
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00117openalex-snapshot
Mild Activation of 2-Pyridyl 1-Thioglycosides as Stable Donors for α-Stereoselective Glycosylation
inferred← citeshttps://doi.org/10.1021/acsomega.3c09761openalex-snapshot
B(C6F5)3-Catalyzed Stereoselective 1,2-cis Arabinofuranosylation with a Conformationally Constrained Donor
inferred← citeshttps://doi.org/10.1021/cs3002513openalex-snapshot
Recent Advances in Transition Metal-Catalyzed Glycosylation
inferred← citeshttps://doi.org/10.1021/ja109932topenalex-snapshot
Synthesis of Docosasaccharide Arabinan Motif of Mycobacterial Cell Wall
inferred← citeshttps://doi.org/10.1021/ja993543lopenalex-snapshot
Arabinofuranosyl Oligosaccharides from Mycobacteria: Synthesis and Effect of Glycosylation on Ring Conformation and Hydroxymethyl Group Rotamer Populations
inferred← citeshttps://doi.org/10.1021/jacs.0c00335openalex-snapshot
Stereospecific Furanosylations Catalyzed by Bis-thiourea Hydrogen-Bond Donors
inferred← citeshttps://doi.org/10.1021/jacs.2c02063openalex-snapshot
Stereoselective 1,2-cis Furanosylations Catalyzed by Phenanthroline
inferred← citeshttps://doi.org/10.1021/jo010910eopenalex-snapshot
Arabinofuranosides from Mycobacteria: Synthesis of a Highly Branched Hexasaccharide and Related Fragments Containing β-Arabinofuranosyl Residues
inferred← citeshttps://doi.org/10.1021/jo501052yopenalex-snapshot
Gold(III)-Catalyzed Glycosidations for 1,2-trans and 1,2-cis Furanosides
inferred← citeshttps://doi.org/10.1021/jo802000popenalex-snapshot
Efficient Chemical Synthesis of a Dodecasaccharidyl Lipomannan Component of Mycobacterial Lipoarabinomannan
inferred← citeshttps://doi.org/10.1021/jo9815406openalex-snapshot
Conversion of Pyranose Glycals to Furanose Derivatives: A New Route to Oligofuranosides
inferred← citeshttps://doi.org/10.1021/ol0490680openalex-snapshot
Preparation, Properties, and Applications of n-Pentenyl Arabinofuranosyl Donors
inferred← citeshttps://doi.org/10.1021/ol400931popenalex-snapshot
Facile Synthesis of β- and α-Arabinofuranosides and Application to Cell Wall Motifs of M. tuberculosis
inferred← citeshttps://doi.org/10.1021/ol4036903openalex-snapshot
Synthesis of a Miniature Lipoarabinomannan
inferred← citeshttps://doi.org/10.1038/ncomms14019openalex-snapshot
[Au]/[Ag]-catalysed expedient synthesis of branched heneicosafuranosyl arabinogalactan motif of Mycobacterium tuberculosis cell wall
inferred← citeshttps://doi.org/10.1038/ncomms14851openalex-snapshot
Total synthesis of mycobacterial arabinogalactan containing 92 monosaccharide units
inferred← citeshttps://doi.org/10.1039/c0ob00989jopenalex-snapshot
Synthesis of arabinofuranose branched galactofuran tetrasaccharides, constituents of mycobacterial arabinogalactan
inferred← citeshttps://doi.org/10.1039/c1cc13134fopenalex-snapshot
Propargyl/methyl furanosides as potential glycosyl donors
inferred← citeshttps://doi.org/10.1039/c4ob01395fopenalex-snapshot
Efficient synthesis of oligosaccharyl 1,2-O-orthoesters from n-pentenyl glycosides and application to the pentaarabinofuranoside of the mycobacterial cell surface
inferred← citeshttps://doi.org/10.1039/c5ob01620gopenalex-snapshot
Zn(OTf) 2 promoted rearrangement of 1,2-cyclopropanated sugars with amines: a convenient method for the synthesis of 3-polyhydroxyalkyl-substituted pyrrole derivatives
inferred← citeshttps://doi.org/10.1039/d4ob01593bopenalex-snapshot
Why is thiol unexpectedly less reactive but more selective than alcohol in phenanthroline-catalyzed 1,2- cis O - and S -furanosylations?
inferred← citeshttps://doi.org/10.1080/07328300903477812openalex-snapshot
Synthesis of 3-Deoxy- d -threopentofuranose 5-Phosphate, a Substrate of Arabinose 5-Phosphate Isomerase
inferred← citeshttps://doi.org/10.1080/07328303.2019.1630839openalex-snapshot
An extensive review of studies on mycobacterium cell wall polysaccharide-related oligosaccharides – part I: Synthetic studies on arabinofuranosyl oligosaccharides
inferred← citeshttps://doi.org/10.1081/car-120016487openalex-snapshot
d -ARABINOFURANOSIDES FROM MYCOBACTERIA: SYNTHESIS AND CONFORMATION
inferred← citeshttps://doi.org/10.1081/car-120026604openalex-snapshot
Regioselectivity in Alkylation Reactions of 1,2‐O‐Stannylene Acetals of d ‐Arabinofuranose
inferred← citeshttps://doi.org/10.1093/glycob/cwr068openalex-snapshot
Synthesis, biological studies of linear and branched arabinofuranoside-containing glycolipids and their interaction with surfactant protein A
inferred← citeshttps://doi.org/10.3390/molecules24193596openalex-snapshot
Synthesis of a Di-Mycoloyl Tri-Arabinofuranosyl Glycerol Fragment of the Mycobacterial Cell Wall, Based on Synthetic Mycolic Acids
inferred← citeshttps://doi.org/10.3390/molecules30153295openalex-snapshot
A Rational Synthesis of a Branched Decaarabinofuranoside Related to the Fragments of Mycobacterial Polysaccharides
inferred← citeshttps://doi.org/10.3987/com-01-9199openalex-snapshot
Studies toward Unique Mycolactone Macrolides from Mycobacterium ulcerans
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