146352-62-7

Upstream product

• 146389-03-9 6-bromo-7-oxabicyclo<2.2.1>hept-5-en-2-one 
• 100-46-9 benzylamine 
• 128503-17-3 (+/-)-(1RS,2SR,4SR)-6-bromo-7-oxabicyclo<2.2.1>hept-5-en-2-endo-ol 

Downstream Products

• 146352-63-8 (+/-)-benzyl N-benzyl,N-<(1RS,2SR,4SR)-6-bromo-7-oxabicyclo<2.2.1>hept-5-en-2-endo-yl>carbamate 
• 146352-64-9 benzyl N-benzyl,N-<(1RS,2SR,4SR,5SR)-5-exo-hydroxy-6-oxo-7-oxabicyclo<2.2.1>hept-2-endo-yl>carbamate 
• 146352-65-0 (+/-)-(1RS,2SR,4SR,5SR)-5-endo-(N-benzyl-N-benzyloxycarbonyl)amino-3-oxo-7-oxabicyclo<2.2.1>hept-2-exo-yl acetate 
• 146352-63-8 benzyl N-benzyl,N-<(1RS,2RS,4SR)-6-bromo-7-oxabicyclo<2.2.1>hept-5-en-2-exo-yl>carbamate 

Relevant academic research and scientific papers

Total asymmetric syntheses of d-lividosamine and 2-acetamido-2,3-dideoxy-d-arabino-hexose derivatives

The "naked sugar" (+)-(1R, 4R)-7-oxabicyclo[2.2.1]hept-5-en-one((+)-2) has been converted to D-lividosamine ((+)-1: 3-deoxy-D-glucosamine) and derivatives via (+)-2-chloro-2,3-dideoxy-5,6-O-isopropyridene-D-arabino-hexono-1,4-lactone ((+)-33) and (+)-2-az