TCI C1327 (2S,8aR)-(-)-(Camphorylsulfonyl)oxaziridine is the enantiomeric counterpart of the widely used camphor-derived chiral oxidant. Its rigid sulfonyl-camphor scaffold delivers oxygen preferentially to one face of the substrate, supporting enantioselective enolate hydroxylation and the preparation of chiral sulfoxides from sulfides. The metal-free oxygen transfer mechanism is valuable when the final product must remain free of transition-metal residues. AMI Scientific offers this reagent in research-scale packaging for organic chemistry, pharmaceutical, and academic laboratories across Indonesia.
TCI brochures (PDF)
- Asymmetric Synthesis 2026-03-18 · p. 6
- Terpenes 2025-09-22 · p. 5
Related TCI products
- TCI C1326 104322-63-6 (2R,8aS)-(+)-(Camphorylsulfonyl)oxaziridine [Asymmetric Oxidizing Reagent]
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- TCI T2579 1208985-45-8 (1S,4S,5S)-4,7,7-Trimethyl-6-thiabicyclo[321]octane
- TCI T2578 5718-75-2 (1R,4R,5R)-4,7,7-Trimethyl-6-thiabicyclo[321]octane
- TCI B4412 55870-50-3 (-)-3-Bromocamphor-8-sulfonic Acid Ammonium Salt
- TCI B1125 14575-84-9 (+)-3-Bromocamphor-8-sulfonic Acid Ammonium Salt
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![(2S,8aR)-(-)-(Camphorylsulfonyl)oxaziridine [Asymmetric Oxidizing Reagent] (CAS 104372-31-8) - TCI C1327 - AMI Scientific](http://amiscientific.com/cdn/shop/files/TCI2510C1327.jpg?v=1767096761&width=1445)
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![5718-75-2 (1R,4R,5R)-4,7,7-Trimethyl-6-thiabicyclo[3.2.1]octane - AMI Scientific](http://amiscientific.com/cdn/shop/files/TCI2510T2578.jpg?v=1767143067&width=533)


