1332585-38-2

Upstream product

• 324767-42-2 (2E,4E)-5-(tert-butoxycarbonylamino)penta-2,4-dienoic acid methyl ester 
• 1332585-33-7 (+)-N-tert-butoxycarbonyl((1R,5R,6S)-4,5,6-tris(acetyloxymethyl)cyclohex-3-en-1-yl)amine 
• 1332585-32-6 N-tert-butoxycarbonyl((1R,5R,6S)-4,5,6-tris(hydroxymethyl)-cyclohex-3-en-1-yl)amine 
• 1332585-31-5 (3S,3aR,7R,7aS)-methyl 7-((tert-butoxycarbonyl)amino)-3-(((1S,2R,5S)-5-methyl-2-(1-methylethyl)cyclohexyl)oxy)-1-oxo-1,3,3a,6,7,7a-hexahydroisobenzofuran-4-carboxylate 
• 1332585-34-8 ((1R,5R,6S)-4,5,6-tris(acetyloxymethyl)cyclohex-3-en-1-yl)-amine 
• 77268-18-9 β-methoxy-α-methylacryloyl isocyanate 

Relevant academic research and scientific papers

Asymmetric synthesis of cyclohexene nucleoside analogues

The asymmetric synthesis of novel cyclohexene nucleoside analogues 12 and 15 is described. An enantiospecific Diels - Alder reaction between (E,E)-diene 2 and (+)-5-(D-mentyloxy)-2(5H)-furanone 3 provided the cycloadduct isomer 4. Three additional steps y