Zhang, Ye published the artcileTotal Synthesis of (-)-Alstofolinine A: Selected Furan Oxidation/ Cyclization Cascade, Product Details of C4H11NOS, the main research area is chemoselective oxidation aza Achmatowicz rearrangement cyclization cascade diastereoselective; alstofolinine A total synthesis.
Indole-fused tetracyclic ring systems containing nitrogen atoms are common core skeletons of many indole alkaloids such as sarpagine, macroline, and ajmaline. Efficient and stereoselective construction of these ring systems can promote the development of the corresponding alkaloid syntheses. In this article, we briefly summarize our current progress toward the application of the aza-Achmatowicz reaction and indole nucleophilic addition reaction cascade for the first asym. total synthesis of the macroline-type indole alkaloid (-)-Alstofolinine A. Our synthetic strategy is based on furan oxidation/rearrangement and proceeds from easily accessible materials such as indole and furan derivatives
Synlett published new progress about Achmatowicz reaction (aza-). 343338-28-3 belongs to class amides-buliding-blocks, name is (S)-2-Methylpropane-2-sulfinamide, and the molecular formula is C4H11NOS, Product Details of C4H11NOS.
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