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Synthesis of the first chiral PNA monomer labelled with a Fischer-type carbene complex
✍ Scribed by Stefano Maiorana; Emanuela Licandro; Dario Perdicchia; Clara Baldoli; Barbara Vandoni; Clelia Giannini; Michele Salmain
- Book ID
- 104422488
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- English
- Weight
- 239 KB
- Volume
- 204-205
- Category
- Article
- ISSN
- 1381-1169
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✦ Synopsis
The synthesis, through a cross-metathesis reaction, of the first chiral peptide nucleic acid (PNA) monomer labelled with a Fischer-type carbene complex of chromium is reported. IR analysis of the new bioconjugate shows that the Cr(CO) 4 moiety represents a suitable spectroscopic probe for diagnostic purposes.
📜 SIMILAR VOLUMES
A new procedure for the synthesis of 1,3,4-trisubstituted and 1,4-disubstituted pyrrolidin-2-one derivatives in an enantioselective fashion is reported. The 1,3-dipolar cycloaddition of (AE)menthol and (À)-8-phenylmenthol derived Fischer alkoxy alkenyl carbene complexes with in situ generated functi
3+2] Cycloaddition of Fischer carbene complexes with nitrilimines is described for the first time, The "onepot" conversion of Fischer carbenes into enantiomerically pure A2-pyrazolines with high regio-and diastereoselectivity is presented as an expeditious route to these compounds.