1976
DOI: 10.1002/chin.197607326
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ChemInform Abstract: ERGOLINE DERIVATIVES. XIII. α‐ADRENERGIC BLOCKING DRUGS

Abstract: Durch Umsetzung von 8‐Hydroxymethyl‐, 8‐Hydroxyäthyl‐ und S‐Aminomethylergolinen mit Bromnicotinsäurechlorid bzw. durch Umwandlung der Alkohole in die entsprechenden Chloride (Tetrachlorkohlenstoff/Triphenylphosphin) und deren Reaktion mit B‐romnicotinsäure‐natriumsalz werden insgesamt 24 neue Ester (II), (III) und (IV) erhalten, die im Vergleich zu Nicergoline (II) zum großen Teil geringere blockierende Wirkung auf adrenerge α‐Rezegtoren haben.

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“…Ergoline derivatives including ethers related to IV have been of interest recently as potential prolactin inhibitors (11) and a-adrenergic blocking agents (12). The manganese dioxide oxidation of elymoclavine in methanol provides a convenient one-step synthesis of IV from a readily available starting material.…”
Section: Discussionmentioning
confidence: 99%
“…Ergoline derivatives including ethers related to IV have been of interest recently as potential prolactin inhibitors (11) and a-adrenergic blocking agents (12). The manganese dioxide oxidation of elymoclavine in methanol provides a convenient one-step synthesis of IV from a readily available starting material.…”
Section: Discussionmentioning
confidence: 99%
“…Ergoline derivatives including ethers related to IV have been of interest recently as potential prolactin inhibitors (11) and a-adrenergic blocking agents (12). The manganese dioxide oxidation of elymoclavine in methanol provides a convenient one-step synthesis of IV from a readily available starting material.…”
Section: Discussionmentioning
confidence: 99%