Work

Chemoselective homologative preparation of trisubstituted alkenyl halides from carbonyls and carbenoids

Year: 2024

Type: article

Abstract: ester, nitrile, nitro, or halogen groups) can be placed on the starting materials, thus documenting a wide reaction scope, as well as the application of the technique to biologically active substances.

Source: Chemical Communications

DOI: 10.1039/d4cc05937a

Authors: Margherita Miele, Davide Castiglione, Wolfgang Holzer, Laura Castoldi, Vittorio Pace

Institutions: University of Turin, University of Vienna, University of Milan

Language: English

Topic: Cyclopropane Reaction Mechanisms

Subfield: Organic Chemistry

Field: Chemistry

Domain: Physical Sciences

Open Access status: hybrid

Funders: Dipartimenti di Eccellenza, Universität Wien, Università degli Studi di Torino

Awards: G1303340219, G2619993990, G4026782726, G5386476940, G683883107

OpenAlex ID: W4405123246

FWCI: 0.972

Cites: 62

Cited by: 7

Related to: 10