Heterobifunctional Cross-Linkers
Heterobifunctional crosslinkers have different reactive groups at both ends. These crosslinkers can not only couple molecules with their respective target functional groups in a single step, but also in a sequential (two-step) manner, minimizing unwanted aggregation or self-coupling. They are often used in biochemical and biomedical research, especially in protein modification, protein coupling, and protein interaction studies.
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
- Enzyme Cleavable Linkers (Cleave Motif)
- Biotins, Streptavidins
- Functionality Creating Reagents
- Functional Group Blocking Reagents
- PEGylation Reagents and PEG Spacers
- Zero-length Crosslinkers
- Albumin Binding Modification Reagents
- Homobifunctional Cross-Linkers
- Copper-free Click Reaction Reagents
- Photo-reactive Crosslinkers
- N-Terminal Cysteine Residue-specific Conjugation Reagents