Pyrrolophenylalkanolamines as animal yield promoters

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

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514376, 514423, 514424, 514426, 514427, 548215, 548230, 548234, 548232, 548517, 548530, 548531, 548532, 548537, 548540, 548541, 548543, 548551, 548556, 548557, 548558, 548561, 548562, 548563, C07D207416, C07D20742, C07D207235, C07D207335

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active

049046799

ABSTRACT:
Pyrrolophenylalkanolamines of the formula ##STR1## R.sup.1 and R.sup.2 represent hydrogen or various radicals, R.sup.3 represents hydrogen, acyl or trialkylsilyl,

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patent: 4407819 (1983-10-01), Kiernan et al.
G. Engelhardt, "Structure-Activity Relationships . . . ", Arzneim-Forsch/Drug Res. 34 (1984) pp. 1625-1633.
Arzneim-Forsch. (Drug Res.) 22, (1972) pp. 860-869.
H. G. Thomas, "Ketone," Houben-Weyl Meth. Org. Chem. V.7/2b, pp. 1876-1885.
"Herstellung semicyclischer . . . ", Houben-Weyl Meth. Org. Chem. V. 6/3 pp. 707-719.
"Aufspaltung von Heterocyclen . . . ", Houben-Weyl Meth. Org. Chem., V. 7/1, pp. 255-273.

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