Synthesis of carbocyclic C-nucleoside analogues from 8,9,10-trinorborn-5-en-2-ol
- 31 December 1985
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 3,p. 393-398
- https://doi.org/10.1039/p19860000393
Abstract
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).This publication has 5 references indexed in Scilit:
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