Chavan, Omprakash S.’s team published research in World Journal of Pharmaceutical Research in 2022 | CAS: 4381-25-3

Comparative study of various synthetic methods of 1,2,3-triazoles via click reaction: a mini review. Recommended basis is Sulfoximine, Bioisosteric. Products is: https://www.ambeed.com/products/50578-18-2.html, 145026-07-9

(S-Methylsulfonimidoyl)benzene (BD302898) 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: 83730-53-4 and 1621962-30-8.

Different derivatives of azides were condensed with different derivatives of terminal alkynes via click condensation reaction to form resp. derivatives of 1,2,3-triazoles in various reaction conditions. Present paper deals with the comparative study of synthesis of derivatives of 1,2,3-triazoles with respect to yield, reaction time and reaction conditions. All products were characterized by spectral data and elemental anal.

Comparative study of various synthetic methods of 1,2,3-triazoles via click reaction: a mini review. Recommended basis is Sulfoximine, Bioisosteric. Products is: https://www.ambeed.com/products/50578-18-2.html, 145026-07-9

Referemce:
Benzoxazole – Wikipedia,
Benzoxazole | C7H5NO – PubChem