A Grignard-Type Phase-Vanishing Method: Generation of Organomagnesium Reagent and Its Subsequent Addition to Carbonyl Compounds

Synlett - Germany
doi 10.1055/s-0034-1380381
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Georg Thieme Verlag KG

Related search

Reaction of Carbonyl Compounds With Organomagnesium Reagent Formed From Methylene Iodide and Magnesium

NIPPON KAGAKU KAISHI
1972English

Chiral Aryl Grignard Reagents-Generation and Reactions With Carbonyl Compounds

Bulletin of the Chemical Society of Japan
Chemistry
1989English

On the Mechanism of the Copper-Catalyzed Enantioselective 1, 4-Addition of Grignard Reagents to A, B-Unsaturated Carbonyl Compounds

English

The Unexpected Formation of a Dihydroisobenzofuran Derivative From the Addition of a Grignard Reagent to a 1,3-Indanedione

Arkivoc
Organic Chemistry
2012English

Yttrium-Mediated Conversion of Vinyl Grignard Reagent to a 1,2-Dimetalated Ethane and Its Synthetic Application

English

The Reductive Amination of Carbonyl Compounds Using Sodium Hydrogentelluride as a Reducing Reagent

Bulletin of the Chemical Society of Japan
Chemistry
1984English

The Effect of the Catalyst on the Selectivity of the Heterogeneous 1,4-Addition of Organomagnesium Compounds to Chalcone

Periodica Polytechnica: Chemical Engineering
Chemical Engineering
2019English

Oxonitriles: A Grignard Addition-Acylation Route to Enamides

English

1, 4-Diazepinone and Pyrrolodiazepinone Syntheses via Homoallylic Ketones From Cascade Addition of a Vinyl Grignard Reagent to A-Aminoacyl-B-Amino Esters

English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy