Lithiation of the 6-dimethylamino-1-azafulvene dimer. A versatile synthesis of 5-substituted pyrrole-2 carboxaldehydes.
- 1 January 1988
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 29 (7) , 777-780
- https://doi.org/10.1016/s0040-4039(00)80207-5
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Photocyclization strategy for the synthesis of antitumor agent CC-1065: synthesis of dideoxy PDE-I and PDE-II. Synthesis of thiophene and furan analogs of dideoxy PDE-I and PDE-IIThe Journal of Organic Chemistry, 1987
- Synthesis of alkylpyrroles by the sodium borohydride reduction of acylpyrrolesThe Journal of Organic Chemistry, 1985
- Metabolites of the marine sponge Laxosuberites speciesThe Journal of Organic Chemistry, 1980
- Heteroatom‐Facilitated LithiationsPublished by Wiley ,1979
- Azafulvenes 3. Cycloaddition Reaction of 6-Amino-1-azafulvene to Electron-deficient Olefin and AcetyleneHETEROCYCLES, 1976
- Synthesis and paratropicity of heteroatom-bridged [17]annulenonesJournal of the Chemical Society, Perkin Transactions 1, 1973
- Carbonyl derivatives of heterocyclic compounds—IIITetrahedron, 1966
- The synthesis and resolution of (±)-tropan-2-oneTetrahedron, 1962
- Über einige Umsetzungen des 2‐Methyl‐3‐carbäthoxy‐pyrrols, des 2‐Methyl‐pyrrols und des 2,3‐Dimethyl‐pyrrolsBerichte der deutschen chemischen Gesellschaft (A and B Series), 1928