Enantioselective synthesis of the carbocyclic nucleosides (-)-aristeromycin and (-)-neplanocin A by a chemicoenzymatic approach
M Arita, K Adachi, Y Ito, H Sawai…
Index: Arita; Adachi; Ito; et al. Journal of the American Chemical Society, 1983 , vol. 105, # 12 p. 4049 - 4055
Full Text: HTML
Citation Number: 182
Abstract
Abstract: An efficient synthesis of the carbocyclic nucleosides (-)-aristeromycin and (-)- neplanocin A has been developed in an enantioselective and stereocontrolled manner starting from the Diels-Alder adduct of cyclopentadiene and dimethyl acetylenedicarboxylate . The symmetric unsaturated dimethyl ester, dimethyl (3aa, 4P, 7P, 7aa)-3a, 4, 7, 7a- tetrahydro-2, 2-di-methyl-4, 7-methanc-1, 3-benzodioxole-5, 6-dicarboxylate, was ...
Related Articles:
[Burlina, Fabienne; Favre, Alain; Fourrey, Jean-Louis; Thomas, Martial Chemical Communications, 1996 , # 14 p. 1623 - 1624]
[Trost; Li; Guile Journal of the American Chemical Society, 1992 , vol. 114, # 22 p. 8745 - 8747]
[Trost; Li; Guile Journal of the American Chemical Society, 1992 , vol. 114, # 22 p. 8745 - 8747]
An expeditious route to carbocyclic nucleosides:(−)-aristeromycin and (−)-carbodine
[Burlina, Fabienne; Favre, Alain; Fourrey, Jean-Louis; Thomas, Martial Bioorganic and Medicinal Chemistry Letters, 1997 , vol. 7, # 3 p. 247 - 250]
An expeditious route to carbocyclic nucleosides:(−)-aristeromycin and (−)-carbodine
[Burlina, Fabienne; Favre, Alain; Fourrey, Jean-Louis; Thomas, Martial Bioorganic and Medicinal Chemistry Letters, 1997 , vol. 7, # 3 p. 247 - 250]