Journal of Medicinal Chemistry p. 739 - 744 (1994)
Update date:2022-08-17
Topics:
Elliot, Robert D.
Rener, Gregory A.
Riordan, James M.
Secrist, John A.
Bennett, L. Lee
et al.
Cyclopentadiene was converted in six steps to the key intermediate (+/-)-(1α,2β,4α)-4-amino-2-(benzyloxy)cyclopentanol (10), which in turn was converted to the carbocyclic nucleoside analogs 14 and 19 by standard procedures developed in these laboratories
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