1246438-65-2

Upstream product

• 74-85-1 ethene 
• 1246438-63-0 (2R,3S,4S,5S)-2-(allyloxy)-2-ethynyl-5-phenyltetrahydrofuran-3,4-diyl diacetate 

Downstream Products

• 1246438-14-1 (2'R,3'S,4'S,5'S)-7-hydroxy-6,11-dioxo-5'-phenyl-4',5',6,11-tetrahydro-1H,3'H-spiro[anthra[2,1-c]furan-3,2'-furan]-3',4'-diyl diacetate 
• 1246438-70-9 (2'R,3'S,4'S,5'S)-10-hydroxy-6,11-dioxo-5'-phenyl-4',5',6,11-tetrahydro-1H,3'H-spiro[anthra[2,1-c]furan-3,2'-furan]-3',4'-diyl diacetate 
• 1246438-71-0 (1'R,3S,4S,5S)-dimethyl 3,4-diacetoxy-5-phenyl-4,5-dihydro-3H,3'H-spiro[furan-2,1'-isobenzofuran]-4',5'-dicarboxylate 
• 1246438-69-6 (2'R,3'S,4'S,5'S)-6,11-dioxo-5'-phenyl-4',5',6,11-tetrahydro-1H,3'H-spiro[anthra[2,1-c]furan-3,2'-furan]-3',4'-diyl diacetate 

Relevant academic research and scientific papers

Application of an enyne metathesis/diels-alder cycloaddition sequence: A new versatile approach to the syntheses of C-Aryl glycosides and spiro- C-Aryl glycosides

An efficient approach for the synthesis of a variety of C-aryl and spiro- C-aryl glycosides is described. This diversity-oriented strategy employed here relies on a sequential enyne metathesis to generate the 1,3-diene moiety and Diels-Alder reaction with