2014European Journal of Organic ChemistryRequires access

Rhodium(I)‐Catalyzed Cycloisomerization of Allene–Allenylcyclopropanes

Takamasa Kawamura, Yasuaki Kawaguchi, Katsuya Sugikubo, Fuyuhiko Inagaki, Chisato Mukai

Open publisher page 23 citations

Abstract

Abstract The RhI‐catalyzed intramolecular [5+2–2]‐type cycloisomerization of allene–allenylcyclopropanes was developed. In this reaction, ethylene was liberated from the cyclopropane ring to afford the 1,5,6,7‐tetrahydroazulene skeletons.

About this research paper

What this paper is about

Abstract The RhI‐catalyzed intramolecular [5+2–2]‐type cycloisomerization of allene–allenylcyclopropanes was developed. In this reaction, ethylene was liberated from the cyclopropane ring to afford the 1,5,6,7‐tetrahydroazulene skeletons.

Why it matters

OpenAlex reports 23 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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 The RhI‐catalyzed intramolecular [5+2–2]‐type cycloisomerization of allene–allenylcyclopropanes was developed. In this reaction, ethylene was liberated from the cyclopropane ring to afford the 1,5,6,7‐tetrahydroazulene skeletons.

Key concepts: Cycloisomerization, Allene, Rhodium, Chemistry, Catalysis, Stereochemistry, Organic chemistry

Related papers

Back to paper searchBrowse research topicsOriginal source
Rhodium(I)‐Catalyzed Cycloisomerization of Allene–Allenylcyclopropanes — Research Paper | ScholarLens