The protected cyclopentanecarboxylic acids (6) and (14), obtained from 8,9,10-trinorborn-5-en-2-ol, are useful intermediates for the synthesis of carbocyclic ribo- and 2′-deoxyribo-C-nucleoside analogues. This is exemplified by their conversion into the imidazo[1,5-a]pyridine carbocyclic C-nucleosides (18) and (22).
R. C. Cookson, P. J. Dudfield and D. I. C. Scopes, J. Chem. Soc., Perkin Trans. 1, 1986, 393 DOI: 10.1039/P19860000393
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