Azidation, Diazo Transfer

Azidation and diazo transfer reagents introduce azide (R-N3) or diazo (R2C=N2) groups into organic molecules. Sulfonyl azides such as p-dodecylbenzenesulfonyl azide transfer a diazo group to active methylene compounds (Regitz diazo transfer) and are safer alternatives to tosyl azide; related reagents convert primary amines into azides.

Technical Resources

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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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Purity: ≥98%

Cat. No. : CS-0031967

CAS No. : 79791-38-1

4-Dodecylbenzensulfonyl azide

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Azidation, Diazo Transfer

Technical Resources

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