211444-70-1

Upstream product

• 211444-56-3 (S)-4-Benzyl-3-((1S,2S,4S)-2-fluoro-bicyclo[2.2.1]hept-5-ene-2-carbonyl)-oxazolidin-2-one 
• 211448-04-3 4-(1R,2S,5R,3'S,4'S,6'S)-[5-methyl-2-(1-methyl-1-phenylethyl)-cyclohexyloxycarbonyl]-4-fluorobicyclo[2.2.1]heptene 
• 211444-62-1 benzyl (1S,2S,4S)-2-fluorobicyclo[2.2.1]hept-5-ene-2-carboxylate 

Downstream Products

• 211444-62-1 benzyl (1S,2S,4S)-2-fluorobicyclo[2.2.1]hept-5-ene-2-carboxylate 

Relevant academic research and scientific papers

Synthesis of 2-fluoro analog of 6-aminonorbornane-2,6-dicarboxylic acid: A conformationally rigid glutamic acid derivative

Synthesis of 2-fluoro analog of 6-aminonorbornane-2,6-dicarboxylic acid, a conformationally restricted analog of glutamic acid, in optically pure form is described.

Asymmetric Diels-Alder reactions of 2-fluoroacrylic acid derivatives. Part 1: The construction of fluorine substituted chiral tertiary carbon

For the construction of chiral monofluorinated tertiary carbons, we have examined the asymmetric Diels-Alder reaction of 2-fluoroacrylic acid derivatives beating a chiral oxazolidinone moiety. Under diethylaluminum chloride catalyzed conditions at - 100°C