Synthesis of (±)-cis-3-aminomethyl-1-tndanylmethanol as a precursor of carbocyclic analogues of nucleosides

Article abstract of DOI:10.1080/15257779908041520

Aminoalcohol precursor of carbocyclic analogues of nucleosides (±)-cis-3-aminomethyl-1-indanylmethanol was efficiently synthesized starting from benzonorbornadiene (5) previously prepared by addition of cyclopentadiene to 1-bromo2-fluorobenzene. Copyright

Full text of DOI:10.1080/15257779908041520

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Nucleosides and Nucleotides
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Synthesis of (±)-cis-3-Aminomethyl-1-
indanylmethanol as a Precursor of
Carbocyclic Analogues of Nucleosides
a
a
a
M. Escobar , F. Fernández , X. García-Mera & J. E. Rodriguez-
a
Borges
a
Dpto. Química Orgánica, Facultad de Farmacia, Universidad de
Santiago, E-15706, Santiago de Compostela, Spain
Version of record first published: 04 Oct 2006
To cite this article: M. Escobar, F. Fernández, X. García-Mera & J. E. Rodriguez-Borges (1999):
Synthesis of (±)-cis-3-Aminomethyl-1-indanylmethanol as a Precursor of Carbocyclic Analogues of
Nucleosides, Nucleosides and Nucleotides, 18:4-5, 625-626
To link to this article: http://dx.doi.org/10.1080/15257779908041520
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