1954
DOI: 10.1021/ja01633a075
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The Synthesis of Certain N,N'-Di-(p-carbomethoxyalkylphenyl)-polymethylenediamines

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Cited by 5 publications
(6 citation statements)
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“…We assign these bands to C=O stretching of TFA based on the work by Fuson et al 46 We also observe a band at ~1452 cm −1 that is assigned to C=O deformation. 46 The bands at ~1014 and 1177 and ~1273 cm −1 are assigned to the OH out-of-plane deformation, C-F stretching, and OH in-plane deformations, respectively, of protonated TFA. 46 We found that the NDQ20 supernatant has a pH of ~+3.5.…”
Section: Soluble Ndq20 Supernatant Fraction Contains a Ppii-like Peptmentioning
confidence: 81%
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“…We assign these bands to C=O stretching of TFA based on the work by Fuson et al 46 We also observe a band at ~1452 cm −1 that is assigned to C=O deformation. 46 The bands at ~1014 and 1177 and ~1273 cm −1 are assigned to the OH out-of-plane deformation, C-F stretching, and OH in-plane deformations, respectively, of protonated TFA. 46 We found that the NDQ20 supernatant has a pH of ~+3.5.…”
Section: Soluble Ndq20 Supernatant Fraction Contains a Ppii-like Peptmentioning
confidence: 81%
“…We assign our UVRR spectrum of protonated TFA based on the assignments of Fuson et al 46 For protonated TFA, the most intense UVRR peaks are found at ~1795 and ~1772 cm −1 .…”
Section: Soluble Ndq20 Supernatant Fraction Contains a Ppii-like Peptmentioning
confidence: 99%
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“…49 where the following values of m, x, and y, are used (1,4,33,35,36,44)]. The inclusion of nitrogen in the paracyclophane ring system has been attempted and failed in all cases investigated (50). A very interesting and potentially useful synthetic method involves the use of thiophene rather than benzene as the aromatic ring upon which the cyclic bridge is built.…”
Section: E Paracyclophanesmentioning
confidence: 99%
“…A number of papers have been published on the conformations of a,fl-unsaturated ketone derivatives. Some of the ketone derivatives are obtained either as the s-cis or as the s-trans form, mainly because of the steric and/or packing effect (Noack & Jones, 1961;Jungk & Schmidt, 1970;Ohkura, Kashino & Haisa, 1973;Rabinovich & Shakked, 1974), and others exist as equilibrium mixtures of different conformers at least in solution (Fuson, Josien & Shelton, 1954;Kronenberg & Havinga, 1965;Hayes & Timmons, 1968;Dimmock, Carter & Ralph, 1968;Silver & Boykin, 1970;Winecoff& Boykin, 1972).…”
Section: Introductionmentioning
confidence: 99%