1258500-83-2

Upstream product

• 1258500-82-1 C₁₈H₂₈O₃Si 
• 6638-79-5 N,O-dimethylhydroxylamine*hydrochloride 
• 1258500-81-0 C₂₈H₃₇NO₄Si 
• 1258500-80-9 C₂₅H₃₃NO₄Si 

Downstream Products

• 1258500-84-3 C₂₅H₄₇NO₄Si₂ 
• 1258500-85-4 C₂₄H₄₄O₃Si₂ 
• 1258500-86-5 C₂₇H₅₀O₃Si₂ 
• 1258500-56-9 C₁₅H₂₂O₃ 
• 1258500-57-0 4-(((2S,3S)-2-methyl-2-(prop-1-en-2-yl)tetrahydrofuran-3-yl)-methyl)phenol 
• 1340478-87-6 (3a'S,6a'S)-6a'-methyl-2'-(phenylthio)-2',3',3a',4',6',6a'-hexahydrospiro[cyclohexa[2,5]diene-1,5'-cyclopenta[b]furan]-4-one 

Relevant academic research and scientific papers

Oxidative prins-pinacol tandem process mediated by a hypervalent iodine reagent: Scope, limitations, and applications

An oxidative Prins-pinacol tandem process mediated by a hypervalent iodine reagent has been developed. This oxidative version of the famous tandem process fits within the concept of "aromatic ring umpolung" and allows the stereoselective transformation of

An oxidative prins-pinacol tandem process and its application to the synthesis of (-)-platensimycin

Center stage: An oxidative Prins-pinacol tandem process mediated by a hypervalent iodine reagent has been accomplished. The strategy allows rapid access to highly functionalized spirocyclic cores (see scheme) present in many natural products. A first application to the formal synthesis of (?)-platensimycin has been achieved.