Staudinger Ligation
Staudinger Ligation refers to the process of using phosphine to react with an active carbonyl group (such as amide or ester) to form an intermediate, and then subsequent chemical transformation to generate a stable connection product. It provides an efficient and specific method for labeling, cross-linking and modification of biomolecules.
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: ≥98%
![1,4-Diazabicyclo[2.2.2]octane|CS-W020025](https://file.chemscene.com/productPIC/CS-W020025.gif)
Cat. No. : CS-W020025 -
In-stockPurity: ≥95%
Cat. No. : CS-0336887CAS No. : 170278-50-9* This product is not sold in the region.
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In-stockPurity: ≥97%
![1,4-Diazabicyclo[2.2.2]octane,97%|CS-0888184](https://file.chemscene.com/productPIC/CS-0888184.gif)
Cat. No. : CS-0888184