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ChemInform Abstract: Epoxyalcohol Route to Hydroxyethylene Dipeptide Isosteres: A New Synthesis of the Diaminoalcohol Core of HIV-Protease Inhibitor ABT-538 (Ritonavir).

โœ Scribed by Fabio Benedetti; Stefano Norbedo


Publisher
John Wiley and Sons
Year
2001
Weight
31 KB
Volume
32
Category
Article
ISSN
0931-7597

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ChemInform Abstract: Asymmetric Dihydrox
โœ Arun K. Ghosh; Dongwoo Shin; Packiarajan Mathivanan ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 31 KB ๐Ÿ‘ 2 views

Asymmetric Dihydroxylation Route to a Dipeptide Isostere of a Protease Inhibitor: Enantioselective Synthesis of the Core Unit of Ritonavir. -An enantioselective synthesis of the core unit of ritonavir is given which uses Sharpless' catalytic asymmetric dihydroxylation reaction as the key step. Rito