119897-90-4

Upstream product

• 119897-85-7 N-<(4,5-dihydro-3-methyl-(5R)-5-isoxazolyl)carbonyl>-(2R)-bornane-10,2-sultam 

Downstream Products

• 142011-79-8 Toluene-4-sulfonic acid (4R,6R)-2,2,6-trimethyl-[1,3]dioxan-4-ylmethyl ester 
• 165689-75-8 benzyl (2R,3R,6S,8R)-nonactate mesylate ester 
• 58166-58-8 benzyl (2R,3R,6S,8R)-nonactate 
• 165689-76-9 benzyl 8-tert-butyldimethylsilyl-(+)-nonactyl-(-)-nonactyl-(+)-nonactyl-(-)-nonactate 
• 159153-49-8 (S)-2-{(2S,5R)-5-[(R)-2-(tert-Butyl-dimethyl-silanyloxy)-propyl]-tetrahydro-furan-2-yl}-propionic acid (S)-2-[(2S,5R)-5-((R)-1-benzyloxycarbonyl-ethyl)-tetrahydro-furan-2-yl]-1-methyl-ethyl ester 

Relevant academic research and scientific papers

Asymmetric silyl nitronate cycloadditions with bornane-10,2-sultam derivatives

Asymmetric silyl nitronate cycloadditions with N-acryloyl (2R)-bornane-10,2-sultam, N-acryloyl (2S)-bornane-10,2-sultam, and N-methacryloyl (2R)-bornane-10,2-sultam have been studied. The asymmetric silyl nitronate cycloaddition/elimination methodology pr

The Preparation of Optically Active Δ2-Isoxazolines. A Model for Asymmetric Induction in the Non Lewis Acid Catalyzed Reactions of Oppolzer's Chiral Sultam

Good diastereoselectivity (ca. 90/10) is reported in the cycloaddition reactions of Oppolzer's chiral sultam with nitrile oxides.A model is proposed which may apply to other non Lewis acid promoted reactions of this sultam.