Protecting Agents for Hydroxy and Amino Groups
Protective nucleoside monomers refer to protective groups used to avoid unnecessary side reactions in chemical reactions when synthesizing nucleosides or nucleic acids. These protective groups play a key role in protecting nucleosides during the synthesis process.
Technical Resources
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Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiralChiral chloro-indeno pybox has served as a new ligand for the Yb(OTf)3-catalyzed asymmetric Friedel–Crafts alkylation reaction of indoles with nitroalkenes. The tunable nature of pybox ligands
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2Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral
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3Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral
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4Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral
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5Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral
Related Classifications
- Methylated Nucleosides
- Phosphorylating Agents, Phosphorothioating Agents
- Coupling Activators, Condensing Agents
- Riboses, 2'-Deoxyriboses
- Sulfur Transfer Reagents
- Protected Nucleosides
- Nucleoside Phosphoramidites
- Peptide Nucleic Acid (PNA) Monomers
- Base Modified Nucleosides and Nucleotides
- 2'-O-Methylribonucleosides