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A metathesis approach to aromatic heterocycles
- Source :
- EUROPEAN JOURNAL OF ORGANIC CHEMISTRY. 2005(10)
- Publication Year :
- 2005
-
Abstract
- The ring closing metathesis (RCM) reaction can be used to prepare substituted furans and pyrroles. By utilising a Pd-catalysed coupling reaction with methoxyallene, allylic alcohols and sulfonamides can be converted into substrates that are ideal precursors to ring closing metathesis. After the RCM reaction is complete, the addition of acid promotes an elimination of methanol to form the fully aromatised system. A range of different substitution patterns and functional groups are compatible with this sequence. Double allene coupling, RCM and elimination reactions are also possible and allow the formation of biaryl systems. © Wiley-VCH Verlag GmbH and Co. KGaA, 69451 Weinheim, Germany, 2005.
- Subjects :
- Allylic rearrangement
Chemistry
Allene
Organic Chemistry
General Medicine
Metathesis
Combinatorial chemistry
Coupling reaction
Elimination reaction
chemistry.chemical_compound
Ring-closing metathesis
Salt metathesis reaction
Organic chemistry
Ring-opening metathesis polymerisation
Methanol
Physical and Theoretical Chemistry
Acyclic diene metathesis
Subjects
Details
- ISSN :
- 10990690 and 1434193X
- Volume :
- 2005
- Issue :
- 10
- Database :
- OpenAIRE
- Journal :
- EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
- Accession number :
- edsair.doi.dedup.....5d87899d3cdd54682d3de9d98ac7049f