81713-02-2

Upstream product

• 81713-00-0 1L-3,4-Di-O-benzyl-1-C-hydroxymethyl-2-O-methyl-5,7-di-O-p-tolylsulfonyl-chiro-inositol 
• 80971-15-9 1L-3,4-Di-O-benzyl-1-C-hydroxymethyl-2-O-methyl-chiro-inositol 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 81713-06-6 2L-(2,3,5/4,6)-4,5-Di-O-benzyl-2-O-methylsulfonyl-6-O-methyl-1-C-methylen-3-O-p-tolylsulfonylpentahydroxycyclohexan 
• 81713-04-4 2L-(2,3,5/4,6)-4,5-Di-O-benzyl-6-O-methyl-1-C-methylen-3-O-p-tolylsulfonylpentahydroxycyclohexan 

Relevant academic research and scientific papers

SYNTHESE VON 7-AMINOVALIENAMIN UND ANDEREN VERZWEIGTEN CONDURITOL-DERIVATEN DURCH -SIGMATROPE UMLAGERUNG

A -sigmatropic rearrangement can occur easily in inositol derivatives bearing an exocyclic methylene group when a substituent capable of migration, e.g., azido, occupies a position vicinal to the double bond.This rearrangement leads to the thermodyna