Palladium-assisted route to carbocyclic nucleosides: A formal synthesis of (±)-aristeromycin
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. The biosynthesis of aristeromycin. Elucidation of the origin of the adenine and cyclopentane rings
2. 9-[β-DL-2α,3α-Dihydroxy-4β-(hydroxymethyl)- cyclopentyl]adenine, the Carbocyclic Analog of Adenosine1,2
3. Transition-metal-controlled synthesis of (.+-.)-aristeromycin and (.+-.)-2',3'-diepi-aristeromycin. An unusual directive effect in hydroxylations
4. A New Route to (−)-Aristeromycin and (−)-Neplanocin Aviathe Asymmetric Diels–Alder Cycloaddition
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