925545-50-2

Upstream product

• 100-39-0 benzyl bromide 
• 925545-70-6 5,5,11-trimethyl-4,6,10-trioxa-11-aza-tricyclo[7.2.1.0^3,7]dodecan-2-ol 
• 4229-44-1 N-methylhydroxyamine hydrochloride 
• 925545-40-0 6-O-benzyl-1,2,3-trideoxy-4,5-O-isopropylidene-D-altro-oct-1-enitol 
• 925545-39-7 6-O-benzyl-1,2,3-trideoxy-4,5:7,8-di-O-isopropylidene-D-altro-oct-1-enitol 
• 925545-38-6 1,2,3-trideoxy-4,5:7,8-di-O-isopropylidene-D-altro-oct-1-enitol 
• 912642-25-2 oct-7-ene-1,2,3,4,5-pentaol 

Downstream Products

• 925545-57-9 2-benzyloxy-3-hydroxy-8-methyl-7-oxa-8-aza-bicyclo[4.2.1]nonan-4-one 
• 925545-56-8 2-benzyloxy-8-methyl-7-oxa-8-aza-bicyclo[4.2.1]nonane-3,4-diol 

Relevant academic research and scientific papers

Stereo- And regioselectivity in an intramolecular nitrone-alkene cycloaddition of hept-6-enoses with a trans-acetonide blocking group

The positional effect of the trans-acetonide blocking group and the effect of the stereochemistry of the substituents on the regio- and stereoselectivity in intramolecular nitrone-alkene cycloaddition (INAC) reactions of hept-6-enoses are reported. Hept-6

trans-acetonide controlled endo-selective intramolecular nitrone-alkene cycloaddition of hept-6-enoses: A facile entry to calystegines, tropanes, and hydroxylated aminocycloheptanes

(Chemical Equation Presented) High-yielding endo-selective intramolecular nitrone-alkene cycloaddition (INAC) reactions of hept-6-enoses controlled by a trans-acetonide to give bridged bicyclo[4.2.1]isoxazolidines exclusively are realized for the first ti