Protected Nucleosides
Protected nucleosides are mainly used in the synthesis of nucleic acids and their derivatives in chemical and biological research. The role of protecting groups is to prevent the active groups of nucleosides (such as hydroxyl, amino, etc.) from undergoing undesirable reactions in chemical reactions, thereby improving the selectivity and yield of the synthesis. They are often used in nucleic acid synthesis, such as the synthesis of DNA or RNA, to ensure that specific reaction steps do not damage the structure of the synthesized part.
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
- Protecting Agents for Hydroxy and Amino Groups
- Phosphorylating Agents, Phosphorothioating Agents
- Coupling Activators, Condensing Agents
- Riboses, 2'-Deoxyriboses
- Sulfur Transfer Reagents
- Nucleoside Phosphoramidites
- Peptide Nucleic Acid (PNA) Monomers
- Base Modified Nucleosides and Nucleotides
- 2'-O-Methylribonucleosides