Boronic Acid Linkers
Boronic acid linkers are functional groups containing a boron atom bonded to a hydroxyl group, and they are used in the synthesis of covalent organic frameworks (COFs) via reversible covalent bonding. These linkers enable the formation of dynamic and self-healing COFs that can adapt to changes in the environment and recover from damage. COFs containing boronic acid linkers often exhibit high selectivity and affinity for specific analytes, making them very useful in applications such as sensing and separations. The reversibility of boronic acid linkages allows the COF properties to be tuned by external stimuli such as temperature or pH. Boronic acid linkers offer a promising approach to develop responsive and adaptable materials with unique functionalities and applications.
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
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In-stockPurity: ≥97%
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In-stockPurity: ≥98%
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In-stockPurity: ≥95%
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In-stockPurity: ≥95%
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In-stockPurity: ≥97%
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In-stockPurity: ≥98%
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In-stockPurity: ≥97%
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In-stockPurity: ≥98%
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