Coupling cyclizations with fragmentations for the preparation of heteroaromatics: quinolines from o-alkenyl arylisocyanides and boronic acids

CJ Evoniuk, M Ly, IV Alabugin - Chemical Communications, 2015 - pubs.rsc.org
Stereoelectronic restrictions on homoallylic ring expansion in alkyne cascades can be
overcome by using alkenes as synthetic equivalents of alkynes in reaction cascades that are …

[PDF][PDF] Coupling cyclizations with fragmentations for the preparation of heteroaromatics: quinolines from o-alkenyl arylisocyanides and boronic acids1

CJ Evoniuk, M Ly, IV Alabugin - Chem. Commun, 2015 - academia.edu
Stereoelectronic restrictions on homoallylic ring expansion in alkyne cascades can be
overcome by using alkenes as synthetic equivalents of alkynes in reaction cascades that are …

Coupling cyclizations with fragmentations for the preparation of heteroaromatics: quinolines from o-alkenyl arylisocyanides and boronic acids

CJ Evoniuk, M Ly, IV Alabugin - Chemical …, 2015 - pubmed.ncbi.nlm.nih.gov
Stereoelectronic restrictions on homoallylic ring expansion in alkyne cascades can be
overcome by using alkenes as synthetic equivalents of alkynes in reaction cascades that are …

Coupling cyclizations with fragmentations for the preparation of heteroaromatics: quinolines from o-alkenyl arylisocyanides and boronic acids.

CJ Evoniuk, M Ly, IV Alabugin - Chemical Communications …, 2015 - europepmc.org
Stereoelectronic restrictions on homoallylic ring expansion in alkyne cascades can be
overcome by using alkenes as synthetic equivalents of alkynes in reaction cascades that are …

[引用][C] Coupling Cyclizations with Fragmentations for the Preparation of Heteroaromatics: Quinolines from O‐Alkenyl Arylisocyanides and Boronic Acids.

CJ Evoniuk, M Ly, IV Alabugin - ChemInform, 2015 - Wiley Online Library

[引用][C] Coupling cyclizations with fragmentations for the preparation of heteroaromatics: quinolines from o-alkenyl arylisocyanides and boronic acids

CJ Evoniuk, M Ly, IV Alabugin - 2015