PlumX Metrics
Embed PlumX Metrics

A novel reaction mode of a η-acyl inserting into a C-C bond: The chemistry associated with vanadium(III) bonded to a meso-octaethyl bis(pyridine)-bis(pyrrole) macrocycle

Organometallics, ISSN: 0276-7333, Vol: 15, Issue: 12, Page: 2685-2687
1996
  • 6
    Citations
  • 0
    Usage
  • 2
    Captures
  • 0
    Mentions
  • 0
    Social Media
Metric Options:   Counts1 Year3 Year

Metrics Details

Article Description

The doubly homologated meso-octaethylpor-phyrinogen 1, containing two pyridine and two pyrrole rings in cis arrangements, allowed the synthesis of highly reactive vanadium(III) organometallics, via the intermediacy of 2, [Et(m-MeCHN)(CH N)(CHN)-Li(THF) ], and 3, [Et(m-MeCHN)(CH N)CHN)V-Cl]. This latter complex has been converted to the corresponding [V-Me] derivative 4, [Et(m-MeCHN)-(CH N)(CHN)V-Me], which undergoes a facile carbonylation to 5, Et(m-MeCHN)(CH N)(CHN)V-OC(CEt )(Me)]. The intermediate η-acyl derivative thus found displayed an unusual carbenoid reactivity inserting into a C-C bond.

Bibliographic Details

Euro Solari; Raffaella Crescenzi; Denis Jacoby; Carlo Floriani; Angiola Chiesi-Villa; Corrado Rizzoli

American Chemical Society (ACS)

Chemistry

Provide Feedback

Have ideas for a new metric? Would you like to see something else here?Let us know