| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1255094 | Chinese Chemical Letters | 2013 | 4 Pages |
Abstract
A reaction between 1,3-dioxo-N-aryl-2,3-dihydro-1H-indene-2-carboxamides, dialkyl acetylenedicarboxylates, and triphenylphosphine or trimethylphosphite is described as a simple and efficient method for the synthesis of 5-hydroxy-4-aryl-2,5-dihydrofuran-2,3-dicarboxylate derivatives.
Graphical abstractA reaction between 1,3-dioxo-N-aryl-2,3-dihydro-1H-indene-2-carboxamides, dialkyl acetylenedicarboxylates, and triphenylphosphine or trimethylphosphite is described as a simple and efficient method for the synthesis of 5-hydroxy-4-aryl-2,5-dihydrofuran-2,3-dicarboxylate derivatives.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Chemistry (General)
![An efficient synthesis of functionalized tetrahydro-1H-indeno[2,1-c]pyridine derivatives by a PPh3-promoted condensation reaction between acetylene esters and 1,3-dioxo-N-aryl-2,3-dihydro-1H-indene-2-carboxamides](/preview/png/1255094.png "First Page Preview: An efficient synthesis of functionalized tetrahydro-1H-indeno[2,1-c]pyridine derivatives by a PPh3-promoted condensation reaction between acetylene esters and 1,3-dioxo-N-aryl-2,3-dihydro-1H-indene-2-carboxamides")
Authors
Mohammad Hossein Mosslemin, Nasim Shams, Hossein Esteghamat, Hossein Anaraki-Ardakani,