1975
DOI: 10.1021/ja00837a054
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.eta.2 Cyclobutadienoid transition metal complexes. Generation and trapping of a cationic .eta.2-cyclobutadiene iron complex

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Cited by 18 publications
(2 citation statements)
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“…(η 2 -Cyclobutadiene)Fp + has been inferred 529 as the reactive intermediate when (η 1 -3-chlorocyclobut-4enyl)(η 5 -cyclopentadienyl)dicarbonyliron ( 307) is treated with AgPF 6 . In the presence of cyclopentadiene and 1,3-diphenylisobenzofuran, it was trapped in the form of the respective Diels-Alder adducts 308 and 309 (eq 85).…”
Section: Activation Of the Two-electron Component (Dienophile)mentioning
confidence: 99%
“…(η 2 -Cyclobutadiene)Fp + has been inferred 529 as the reactive intermediate when (η 1 -3-chlorocyclobut-4enyl)(η 5 -cyclopentadienyl)dicarbonyliron ( 307) is treated with AgPF 6 . In the presence of cyclopentadiene and 1,3-diphenylisobenzofuran, it was trapped in the form of the respective Diels-Alder adducts 308 and 309 (eq 85).…”
Section: Activation Of the Two-electron Component (Dienophile)mentioning
confidence: 99%
“…Compounds 2l and 2m, e.g., are derived from eugenol (essential oil of clove [18]) and would be difficult to prepare by classical methods [19] in which the allyl moiety is altered. In the literature [19], electrophilic substitutions with eugenol are performed with a protected allyl group, which otherwise reacts with electrophiles, leading to loss of biological activity. Under −classical× conditions (HCl/MeOH solution), side reactions dominate, as shown in Scheme 3.…”
Section: Ohmentioning
confidence: 99%