Substituent-directed aralkylation and alkylation reactions of the tricyclic analogues of acyclovir and guanosine

Article abstract of DOI:10.1080/15257770008045468

Aryl or tert-butyl substituent in the 6 position of 3,9-dihydro-3-[(2-hydroxyethoxy)methyl]-9-oxo-6-R-5H-imidazo[1,2-a]purine (6-R-TACV)¹1 partly directs aralkylation reactions into unusual positions: N-4 to give 3 and C-7 to give N-5,7-disubst

Full text of DOI:10.1080/15257770008045468

Nucleosides, Nucleotides and Nucleic Acids
ISSN: 1525-7770 (Print) 1532-2335 (Online) Journal homepage: http://www.tandfonline.com/loi/lncn20
Substituent — Directed Aralkylation and Alkylation
Reactions of the Tricyclic Analogues of Acyclovir
and Guanosine
Tomasz Ostrowski , Joanna Zeidler , Tomasz Goslinski & Bozenna
Golankiewicz
To cite this article: Tomasz Ostrowski , Joanna Zeidler , Tomasz Goslinski & Bozenna
Golankiewicz (2000) Substituent — Directed Aralkylation and Alkylation Reactions of the
Tricyclic Analogues of Acyclovir and Guanosine, Nucleosides, Nucleotides and Nucleic Acids,
19:10-12, 1911-1929, DOI: 10.1080/15257770008045468
To link to this article: http://dx.doi.org/10.1080/15257770008045468
Published online: 17 Apr 2008.
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Date: 05 November 2015, At: 20:06