Amanote Research
Register
Sign In
1, 4-Diazepinone and Pyrrolodiazepinone Syntheses via Homoallylic Ketones From Cascade Addition of a Vinyl Grignard Reagent to A-Aminoacyl-B-Amino Esters
doi 10.1021/ol061036k.s003
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
Peptide Syntheses via Amino Acid Active Esters
The Unexpected Formation of a Dihydroisobenzofuran Derivative From the Addition of a Grignard Reagent to a 1,3-Indanedione
Arkivoc
Organic Chemistry
Diastereo- And Enantioselective Reductive Aldol Addition of Vinyl Ketones via Catalytic Hydrogenation
Synthesis
Organic Chemistry
Catalysis
Yttrium-Mediated Conversion of Vinyl Grignard Reagent to a 1,2-Dimetalated Ethane and Its Synthetic Application
On the Mechanism of the Copper-Catalyzed Enantioselective 1, 4-Addition of Grignard Reagents to A, B-Unsaturated Carbonyl Compounds
An Asymmetric Vinylogous Michael Cascade of Silyl Glyoximide, Vinyl Grignard, and Nitroalkenes via Long Range Stereoinduction
A Free Radical Cascade Difunctionalization of O‐Vinylanilides With Simple Ketones and Esters
Asian Journal of Organic Chemistry
Organic Chemistry
A Grignard-Type Phase-Vanishing Method: Generation of Organomagnesium Reagent and Its Subsequent Addition to Carbonyl Compounds
Synlett
Organic Chemistry
Highly Enantioselective Michael Addition of Cyclic 1, 3-Dicarbonyl Compounds to A, B-Unsaturated Ketones
