2006
DOI: 10.1016/j.inoche.2005.10.027
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The synthesis and structural characterization of novel N-meta-ferrocenyl benzoyl dipeptide esters

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Cited by 17 publications
(18 citation statements)
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References 34 publications
(48 reference statements)
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“…In our laboratory, we have synthesized various ferrocene derivatives incorporating natural amino acids and dipeptides [16][17][18][19][20][21][22]. We have incorporated three key moieties in the synthesis of these unusual biological materials, namely: (i) an electroactive core, (ii) a conjugated linker that lowers the oxidation potential of the ferrocene moiety, and (iii) an amino acid or peptide derivative that can interact with other molecules via hydrogen bonding.…”
Section: Introductionmentioning
confidence: 99%
“…In our laboratory, we have synthesized various ferrocene derivatives incorporating natural amino acids and dipeptides [16][17][18][19][20][21][22]. We have incorporated three key moieties in the synthesis of these unusual biological materials, namely: (i) an electroactive core, (ii) a conjugated linker that lowers the oxidation potential of the ferrocene moiety, and (iii) an amino acid or peptide derivative that can interact with other molecules via hydrogen bonding.…”
Section: Introductionmentioning
confidence: 99%
“…All the proton and carbon chemical shifts for compounds 2-5 were unambiguously assigned by a combination of DEPT-135 and 1 H-13 C-COSY (HMQC). The 1 H and 13 C NMR spectra for compounds 2-5 showed peaks in the ferrocene region characteristic of a ferrocenyl benzoyl moiety[32][33][34][35][36]. The protons in the ortho position of the (g5 -C 5 H 4 ) ring appear in the region d 4.61 to d 4.64 whereas the protons in the meta position occur in the range d 4.3 to d 4.32.…”
mentioning
confidence: 98%
“…We recently reported the synthesis and structural characterization of a series of N-para, N-meta, and N-ortho-ferrocenyl benzoyl amino acid and N-meta-ferrocenyl benzoyl dipeptide ester derivatives. [32][33][34][35][36].…”
mentioning
confidence: 99%
“…The aminophosphonates 4a-e also were converted into their dipeptide analogues 6a-e in reaction with N-tert-butoxycarbonyl-L-phenylalanine in presence of N-hydroxybenzotriazole (HOBt) and N,N 0 -dicyclohexylcarbodiimide (DCC) as coupling reagents (Scheme 3) [22]. The above mentioned synthesis of compounds 6a-e is an example how to incorporate fluorinated aminophosphonate moieties into peptide chain.…”
Section: Resultsmentioning
confidence: 99%