1-Substituted 2′-deoxyinosine analogues
LD Napoli
Index: De Napoli, Lorenzo; Messere, Anna; Montesarchio, Daniela; Piccialli, Gennaro; Varra, Michela Journal of the Chemical Society - Perkin Transactions 1, 1997 , # 14 p. 2079 - 2082
Full Text: HTML
Citation Number: 28
Abstract
The base 2-carbon of 2′, 3′-di-O-acetyl-2′-deoxyinosine is strongly activated towards nucleophilic attack when either the 4-nitrophenyl or 2, 4-dinitrophenyl group is attached to its N-1 position (product 1 or 2). 1-(ω-Aminoalkyl)-and 1-(ω-hydroxyalkyl)-2′-deoxyinosine derivatives 5, 8–10 have been efficiently synthesized by a rearrangement of the purine ring upon treatment of compound 1 or 2 with the appropriate α, ω-diamine or α, ω- ...
Related Articles:
[Fernandez-Forner, Dolors; Eritja, Ramon; Bardella, Francesc; Ruiz-Perez, Catalina; Solans, Xavier; et al. Tetrahedron, 1991 , vol. 47, # 42 p. 8917 - 8930]
[Fernandez-Forner, Dolors; Eritja, Ramon; Bardella, Francesc; Ruiz-Perez, Catalina; Solans, Xavier; et al. Tetrahedron, 1991 , vol. 47, # 42 p. 8917 - 8930]
[Fernandez-Forner, Dolors; Eritja, Ramon; Bardella, Francesc; Ruiz-Perez, Catalina; Solans, Xavier; et al. Tetrahedron, 1991 , vol. 47, # 42 p. 8917 - 8930]
[Minakawa; Sasabuchi; Kiyosue; Kojima; Matsuda Chemical and Pharmaceutical Bulletin, 1996 , vol. 44, # 2 p. 288 - 295]
[Minakawa; Sasabuchi; Kiyosue; Kojima; Matsuda Chemical and Pharmaceutical Bulletin, 1996 , vol. 44, # 2 p. 288 - 295]