2015ChemInformRequires access

ChemInform Abstract: Highly Selective Directed Arylation Reactions via Back‐to‐Back Dehydrogenative C—H Borylation/Arylation Reactions.

Eric C. Keske, Brandon d. Moore, Olena V. Zenkina, Ruiyao Wang, G. Schatte, Cathleen M. Crudden

Open publisher page 0 citations

Abstract

Abstract Pinacol borylation of 2‐arylpyridines is achieved in the presence of dimeric rhodium NHC complexes.

About this research paper

What this paper is about

Abstract Pinacol borylation of 2‐arylpyridines is achieved in the presence of dimeric rhodium NHC complexes.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Abstract Pinacol borylation of 2‐arylpyridines is achieved in the presence of dimeric rhodium NHC complexes.

Key concepts: Borylation, Chemistry, Pinacol, Rhodium, Combinatorial chemistry, Medicinal chemistry, Organic chemistry, Catalysis

Related papers

Back to paper searchBrowse research topicsOriginal source
ChemInform Abstract: Highly Selective Directed Arylation Reactions via Back‐to‐Back Dehydrogenative C—H Borylation/Arylation Reactions. — Research Paper | ScholarLens