Site-selective photoredox reactions with somophiles readily enable branching of the carbon skeleton of unprotected glucosides, allosides, and xylosides regioselectively at C3. These reactions open the possibility of selective C-C bond formation in monosaccharides without multi-step protection-deprotection strategies.</p
Photodecarboxylation-alkylation of conformationally locked monosaccharides leads to inversion of ste...
Photodecarboxylation-alkylation of conformationally locked monosaccharides leads to inversion of ste...
To circumvent protecting groups, the site-selective modification of unprotected glycosides is intens...
Site-selective photoredox reactions with somophiles readily enable branching of the carbon skeleton ...
Site-selective photoredox reactions with somophiles readily enable branching of the carbon skeleton ...
Site-selective photoredox reactions with somophiles readily enable branching of the carbon skeleton ...
Site-selective photoredox reactions with somophiles readily enable branching of the carbon skeleton ...
Site-selective photoredox reactions with somophiles readily enable branching of the carbon skeleton ...
Site-selective photoredox reactions with somophiles readily enable branching of the carbon skeleton ...
Thioglycosides or S-linked-glycosides are important glycomimetics. These thioglycosides are often pr...
Thioglycosides or S-linked-glycosides are important glycomimetics. These thioglycosides are often pr...
Thioglycosides or S-linked-glycosides are important glycomimetics. These thioglycosides are often pr...
Thioglycosides or S-linked-glycosides are important glycomimetics. These thioglycosides are often pr...
Photodecarboxylation-alkylation of conformationally locked monosaccharides leads to inversion of ste...
Photodecarboxylation-alkylation of conformationally locked monosaccharides leads to inversion of ste...
Photodecarboxylation-alkylation of conformationally locked monosaccharides leads to inversion of ste...
Photodecarboxylation-alkylation of conformationally locked monosaccharides leads to inversion of ste...
To circumvent protecting groups, the site-selective modification of unprotected glycosides is intens...
Site-selective photoredox reactions with somophiles readily enable branching of the carbon skeleton ...
Site-selective photoredox reactions with somophiles readily enable branching of the carbon skeleton ...
Site-selective photoredox reactions with somophiles readily enable branching of the carbon skeleton ...
Site-selective photoredox reactions with somophiles readily enable branching of the carbon skeleton ...
Site-selective photoredox reactions with somophiles readily enable branching of the carbon skeleton ...
Site-selective photoredox reactions with somophiles readily enable branching of the carbon skeleton ...
Thioglycosides or S-linked-glycosides are important glycomimetics. These thioglycosides are often pr...
Thioglycosides or S-linked-glycosides are important glycomimetics. These thioglycosides are often pr...
Thioglycosides or S-linked-glycosides are important glycomimetics. These thioglycosides are often pr...
Thioglycosides or S-linked-glycosides are important glycomimetics. These thioglycosides are often pr...
Photodecarboxylation-alkylation of conformationally locked monosaccharides leads to inversion of ste...
Photodecarboxylation-alkylation of conformationally locked monosaccharides leads to inversion of ste...
Photodecarboxylation-alkylation of conformationally locked monosaccharides leads to inversion of ste...
Photodecarboxylation-alkylation of conformationally locked monosaccharides leads to inversion of ste...
To circumvent protecting groups, the site-selective modification of unprotected glycosides is intens...
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