Abstract: The present invention relates to novel substituted pyridines/pyrimidines of the formula I
where A is CH or N; X is NH, oxygen or S(O)q where q is 0, 1 or 2; Y is a direct bond or CH2; Z is oxygen, NR7 or S(O)m is 0, 1 or 2, and the radicals R1, R2, R3, R4, R5, R6 and R7 are as defined in the description, to processes for their preparation, and to their use as pesticides, fungicides, ovicides or as veterinary medicaments.
Type:
Grant
Filed:
April 1, 1997
Date of Patent:
March 27, 2001
Assignee:
Hoechst Schering
Inventors:
Ralf Braun, Wolfgang Schaper, Werner Knauf, Ulrich Sanft, Manfred Kern, Werner Bonin
Abstract: A compound of formula I or a physiologically acceptable salt thereof ##STR1## wherein X represents sulphur or methylene, R.sub.1 represents hydrogen, amino or an acylated or carbamylated amino group, R.sub.2 represents hydrogen or an alkyl group and R.sub.3 represents an alkoxy group.
Type:
Grant
Filed:
August 22, 1985
Date of Patent:
February 2, 1988
Assignee:
National Research Development Corporation
Abstract: A biologically active compound can be solubilized by reaction in different sequences to form a derivative carrying the active moiety, a linking group such as an optionally substituted diisocyanate radical, a polyether moiety such as a polyoxyethylene radical, and a terminal group such as a butyl radical, e.g. ##STR1## n=1 to 400. The active materials can be agricultural chemicals, pharmaceuticals, and the like.
Type:
Grant
Filed:
December 28, 1979
Date of Patent:
August 4, 1987
Assignee:
Bayer Aktiengesellschaft
Inventors:
Edgar Mohring, Hanns P. Muller, Peter Roessler, Kuno Wagner, Helmut Tietz
Abstract: .beta.-Lactam antibiotics having an .alpha.-formamido substituent on the carbon atom adjacent to the carbonyl group of the .beta.-lactam ring and in particular bicyclic compounds having the partial structure: ##STR1## Intermediates and processes for the preparation of the compounds are further disclosed.