81713-03-3

Upstream product

• 81713-01-1 1L-1,7-Anhydro-2,3,4-tri-O-benzyl-1-C-hydroxymethyl-5-O-p-tolylsulfonyl-chiro-inositol 
• 81712-99-4 1L-2,3,4-Tri-O-benzyl-1-C-hydroxymethyl-5,7-di-O-p-tolylsulfonyl-chiro-inositol 
• 75348-12-8 1L-2,3,4-Tri-O-benzyl-1-C-hydroxymethyl-chiro-inositol 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 81739-83-5 7-Aminovalienamin 
• 81713-11-3 (1R,4R,5S,6S)-3-Aminomethyl-4,5,6-tris-benzyloxy-cyclohex-2-enylamine 
• 81713-05-5 2L-(2,3,5/4,6)-4,5,6-Tri-O-benzyl-1-C-methylen-2-O-methylsulfonyl-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