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http://dx.doi.org/10.1016/j.jaad.2024.05.093 | DOI Listing |
Sci Rep
January 2025
Chemistry Department, Faculty of Science, Tanta University, Tanta, 31527, Egypt.
In a quest to innovate biologically active molecules, the benzoylation of 4,6-dimethylpyrimidine-2-thiol hydrochloride (1) with benzoyl chloride derivatives was employed to produce a series of pyrimidine benzothioate derivatives (2-5). Subsequent sulfoxidation of these derivatives (2-5) using hydrogen peroxide and glacial acetic acid yielded a diverse array of pyrimidine sulfonyl methanone derivatives (6-9). In parallel, the sulfoxidation of pyrimidine sulfonothioates (10-12) yielded sulfonyl sulfonyl pyrimidines (13-15), originating from the condensation of compound 1 with sulfonyl chloride derivatives.
View Article and Find Full Text PDFJ Invest Dermatol
October 2024
Valisure, LLC, New Haven, Connecticut, USA; Arnold & Marie Schwartz College of Pharmacy and Health Sciences, Long Island University, Long Island, New York, USA.
J Am Acad Dermatol
December 2024
Department of Dermatology, Weill Cornell Medicine, New York, New York. Electronic address:
Cutis
July 2024
JDR Dermatology Research, Las Vegas, Nevada; Advanced Dermatology & Cosmetic Surgery, Maitland, Florida; and Touro University Nevada, Henderson.
J Am Acad Dermatol
November 2024
Department of Dermatology, Brigham and Women's Hospital, Boston, Massachusetts. Electronic address:
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