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October 1, 1980Die Makromolekulare Chemie

Stufenweise darstellung eines cycloheptamers aus p‐kresol, 4‐tert‐butylphenol und formaldehyd. Vergleich mit einem phenolischen, heptanuklearen kettenoligomer

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Authors

HKHermann KämmererDarmstadt University of Applied SciencesGHGünter HappelJohannes Gutenberg University Mainz

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Cite This Study

Kämmerer et al. (1980) studied this question.

synapsesocial.com/papers/6a8a7c5351cd0cd12ac151a1https://doi.org/10.1002/macp.1980.021811003
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Also Consider

Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1THET-BUTYL GROUP AS A POSSIBLE PROTECTIVE GROUP IN THE SYNTHESIS OF OLIGO [HYDROXY-1,3-PHENYLENE]METHYLENES1978 · 23 citations
  2. 2Calixarenes. 1. Analysis of the product mixtures produced by the base-catalyzed condensation of formaldehyde with para-substituted phenols1978 · 272 citations
  3. 3Phenol‐formaldehyde and allied resins VI: Rational synthesis of a ‘cyclic’ tetranuclear p‐cresol novolak1958 · 65 citations