Chandrasekhar, Srivari; Rajesh, Gontla; Naresh, Tumma published the artcile< Enantioselective synthesis of the C5-C23 segment of biselyngbyaside>, Name: (S)-4-Benzylthiazolidine-2-thione, the main research area is enantioselective synthesis biselyngbyaside C5 C23 segment addition aldol epoxidation; Julia Kocienski olefination enantioselective synthesis biselyngbyaside C5 C23 segment; Sharpless asym epoxidation enantioselective synthesis biselyngbyaside C5 C23 segment.
Stereo and enantioselective synthesis of C5-C23 fragment I of cytotoxic marine natural product biselyngbyaside is achieved using E-selective Me lithium addition onto enyne, Crimmins’ acetate aldol reaction, Sharpless asym. epoxidation, and Julia-Kocienski olefination as the key steps.
Tetrahedron Letters published new progress about Addition reaction. 171877-39-7 belongs to class thiazole, and the molecular formula is C10H11NS2, Name: (S)-4-Benzylthiazolidine-2-thione.
Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica