Artigo Acesso aberto Revisado por pares

Palladium-catalyzed cross-coupling of 2-iodoadenosine with terminal alkynes: Synthesis and biological activities of 2-alkynyladenosines.

1985; Pharmaceutical Society of Japan; Volume: 33; Issue: 4 Linguagem: Inglês

10.1248/cpb.33.1766

ISSN

1347-5223

Autores

Akira Matsuda, Misao Shinozaki, Tadashi Miyasaka, Haruhiko Machida, Tohichi Abiru,

Tópico(s)

Click Chemistry and Applications

Resumo

Reaction of 2-iodoadenosine (2) with terminal alkynes in the presence of bis (triphenylphosphine) palladium dichloride and cuprous iodide in triethylamine and N, N, -dimethylformamide gave 2-alkynyl-adenosines (3a-h) in excellent yields. Several compounds showed high activity as inhibitors in rat passive cutaneous anaphylaxis (PCA) reaction. Among them, 2-(3-hydroxypropynyl)- and 2-(3-hydroxybutynyl)-adenosines (3d, f) are much more potent than disodium cromoglycate (DSCG).

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