Sulfur Transfer Reagents
Sulfur transfer reagents are widely used in organic synthesis, biochemical research, and materials science by facilitating the transfer of sulfur atoms. These reagents help generate or modify sulfur-containing compounds and play an important role in catalysis, molecular labeling, and structural modification.
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
- Protected Nucleosides
- Nucleoside Phosphoramidites
- Peptide Nucleic Acid (PNA) Monomers
- Base Modified Nucleosides and Nucleotides
- 2'-O-Methylribonucleosides