๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

ChemInform Abstract: A Convenient Synthesis of Enaminones Using Tandem Acetonitrile Condensation, Grignard Addition.

โœ Scribed by A. R. HAIGHT; T. L. STUK; J. A. MENZIA; T. A. ROBBINS


Book ID
101853378
Publisher
John Wiley and Sons
Year
2010
Weight
28 KB
Volume
28
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


A convenient synthesis of enaminones usi
โœ Anthony R. Haight; Timothy L. Stuk; Jerome A. Menzia; Timothy A. Robbins ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 170 KB

Ritonavir (Norvirยฎ), 1, is an H1V-I protease inhibitor that recently received FDA regulatory approval for the treatment of HIV infection. I Retrosynthetically, Ritonavir requires the pseudosymmetric diaminoalcohol core unit 2. 2 We recently reported an efficient route for the large scale synthesis

ChemInform Abstract: Addition Reactions
โœ T. T. SHAWE; D. B. HANSEN; K. A. PEET; A. S. PROKOPOWICZ; P. M. ROBINSON; A. CAN ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 32 KB ๐Ÿ‘ 2 views

Addition Reactions of Cyclic s-trans-Enaminones with Grignard Reagents. -Depending on the solvent polarity and coordinating ability, the title reaction leads to 3-alkylcycloalkenones and bis-adducts. Addition of phenylmagnesium bromide gives 3-phenyl substituted cycloalkenones without regard to the