Synthesis and Reactivity of Manganese Tricarbonyl Complexes of the Centropolyindanes 10-Methyltribenzotriquinacene and Fenestrindane (Articolo in rivista)

Type

• Prodotto della ricerca (Classe)
• Articolo in rivista (Classe)

Label

• Synthesis and Reactivity of Manganese Tricarbonyl Complexes of the Centropolyindanes 10-Methyltribenzotriquinacene and Fenestrindane (Articolo in rivista) (literal)

Anno

• 2000-01-01T00:00:00+01:00 (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi

• 10.1021/om000114j (literal)

Alternative label

• Dullaghan C, A., Carpenter G. B., Kuck D., Fusco C., Curci R., Sweigart D. A. (2000)
  Synthesis and Reactivity of Manganese Tricarbonyl Complexes of the Centropolyindanes 10-Methyltribenzotriquinacene and Fenestrindane
  in Organometallics
  (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori

• Dullaghan C, A., Carpenter G. B., Kuck D., Fusco C., Curci R., Sweigart D. A. (literal)

Pagina inizio

• 2233 (literal)

Pagina fine

• 2236 (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume

• 19 (literal)

Rivista

• Organometallics (Rivista)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali

• 4 (literal)

Note

• ISI Web of Science (WOS) (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni

• Department of Chemistry, Brown University, Providence, Rhode Island 02912 Fakultät für Chemie, Universität Bielefeld, Universitätsstrasse 25, D-33615 Bielefeld, Germany CNR Centre MISO, Department of Chemistry, University of Bari, Via Amendola 173, Bari, Italy 70126 (literal)

Titolo

• Synthesis and Reactivity of Manganese Tricarbonyl Complexes of the Centropolyindanes 10-Methyltribenzotriquinacene and Fenestrindane (literal)

Abstract

• The cationic manganese tricarbonyl moiety is readily coordinated to an arene ring of the centropolyindanes 10-methyltribenzotriquinacene (MTBT) and fenestrindane (FET) to afford [(MTBT)Mn(CO)(3)](+) (1) and [(FET)Mn(CO)(3)](+) (2). An X-ray structure of 1 shows that the metal is coordinated to the convex face of the MTBT ligand. Both 1 and 2 are electrophilically activated and readily undergo regioselective and stereoselective addition reactions with mild nucleophiles. (literal)

Prodotto di

• processi e metodologie sostenibili in chimica organica per la sintesi di nuove piattaforme molecolari (PM.P03.011.001) (Modulo)
• Institute of chemistry of organometallic compounds (ICCOM) (Istituto)

Autore CNR

• CATERINA FUSCO (Persona)

Incoming links:

Prodotto

• Institute of chemistry of organometallic compounds (ICCOM) (Istituto)
• processi e metodologie sostenibili in chimica organica per la sintesi di nuove piattaforme molecolari (PM.P03.011.001) (Modulo)

Autore CNR di

• CATERINA FUSCO (Persona)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#rivistaDi

• Organometallics (Rivista)