𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: Asymmetric Synthesis of 1,2,3,4,5,6-Hexahydro-5-hydroxypyrimidin-2-ones as Potential HIV-Protease Inhibitors.

✍ Scribed by Dieter Enders; Lars Wortmann; Barbara Duecker; Gerhard Raabe


Publisher
John Wiley and Sons
Year
2010
Weight
33 KB
Volume
30
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Asymmetric Synthesis of 1,2,3,4,5,6-Hexa
✍ Dieter Enders; Lars Wortmann; Barbara DΓΌcker; Gerhard Raabe πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 German βš– 101 KB πŸ‘ 1 views

The first asymmetric synthesis of potential cyclic urea HIV protease inhibitors of Type 2 is reported. The synthesis is short and highly versatile in the choice of the substitution pattern and absolute configuration of the products starting from readily available materials. Nonchiral central buildin

ChemInform Abstract: 5,6-Dihydropyran-2-
✍ Frederick E. Boyer; et al. et al. πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 36 KB

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v

ChemInform Abstract: Nonpeptidic HIV Pro
✍ J. V. N. Vara Prasad; et al. et al. πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 33 KB

Nonpeptidic HIV Protease Inhibitors: 6-Alkyl-5,6-dihydropyran-2-ones Possessing a Novel and Achiral 3-(2-t-Butyl-5-methyl-4sulfamate)phenylthio Moiety. -With the introduction of a sulfamate moiety, a new template is created which shows HIV protease binding affinity. An alkyl group at the 6-position