Miao, Jinmin’s team published research in Chemical Communications (Cambridge, United Kingdom) in 2014 | CAS: 145026-07-9

Rhodium-catalyzed direct synthesis of unprotected NH-sulfoximines from sulfoxides. Recommended basis is Sulfoximine, Bioisosteric. Products is: https://www.ambeed.com/products/1621962-30-8.html, 50578-18-2

1-Bromo-4-(S-methylsulfonimidoyl)benzene (BD336512) is a building block containing a sulfoximine group. Several CDK and ATR inhibitors have exemplified the utilization of the NH sulfoximine group as abioisostere for a sulfonamide group to overcome the main project hurdles of aqueous solubility, sulfonamide-mediated off-target activity and IP. Moreover, its NH group could be expediently further functionalized through Buchwald-Hartwig coupling reaction and multifarious nucleophilic reactions.. Recommended Products is: 4381-25-3 and 83730-53-4.

A novel rhodium-catalyzed imination of sulfoxides using O-(2,4-dinitrophenyl)hydroxylamine is developed under mild conditions with good functional group tolerance. This method provides an efficient access to free NH-sulfoximines, an important structural unit in a variety of biol. active compounds E.g., in presence of Rh2(esp)2 and O-(2,4-dinitrophenyl)hydroxylamine in trifluoroethanol, imination of sulfoxide derivative (I) gave 84% sulfoximine derivative (II).

Rhodium-catalyzed direct synthesis of unprotected NH-sulfoximines from sulfoxides. Recommended basis is Sulfoximine, Bioisosteric. Products is: https://www.ambeed.com/products/1621962-30-8.html, 50578-18-2

Referemce:
Benzoxazole – Wikipedia,
Benzoxazole | C7H5NO – PubChem