Aldehyde Reactive Fluorophores and Labels

Aldehyde-reactive fluorescent dyes form stable complexes by covalently binding to amino, hydroxyl and other functional groups in biomolecules. This reaction usually involves the formation of imine or ether bonds to achieve labeling. These fluorescent markers have a wide range of applications in biomedical research, cell imaging, protein labeling and other chemical analysis.

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Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral

Chiral 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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Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral
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Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral
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Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral
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Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral

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Aldehyde Reactive Fluorophores and Labels

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Aldehyde Reactive Fluorophores and Labels

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