IN WHICH X IS OXYGEN OR SULFUR, Y IS OXYGEN OR SULFUR, R IS ALKYL, R1 IS ALKYL, R2 IS ALKYL OR ALKOXY AND R3 IS A HETEROCYCLIC GROUP, AND THEIR USE AS INSECTICIDES AND ACARICIDES ARE DISCLOSED.
Abstract:
NOVEL OXIMINO ESTERS OF PARA-SUBSTITUTED-PHENYL PHOSPHORUS AND THIOPHOSPHORUS COMPOUNDS HAVE THE FORMULA
1-(R1-C(-R2)=N-O-P(-Z)(=Y)-O-),4-X-BENZENE
WHEREIN X IS NITRO, CYANO, AZIDE, TRIHALOMETHYL, CARBOALKOXY OR ALKANSEUFONYL; Y IS O OR S; R1 AND R2 CAN BE THE SAME OR DIFFERENT AND ARE SELECTED FROM THE GROUP CONSISTING OF H, ALKYL RADICALS OF 1-6 C ATOMS AND PHENYL; AND Z IS SELECTED FROM THE GROUP CONSISTING OF ALKALYL AND ALKOXY RADICALS EACH HAVING 1-6 C ATOMS, PHENYL, CL AND
-O-N=C(-R3)-R4
WHEREIN R3 AND R4 ARE AS DEFINED FOR F1 AND R2. MANY OF THESE COMPOUNDS ARE PREPARED BY REACTING AN OXIME WITH EITHER A PARA-SUBSTITUTED-PHENYL PHOSPHOROCHLORIDATE. A SIMILARLY SUBSTITUTED THIOPHOSPHOROCHLORIDATE OR PHENYLTHIOPHOSPHONIC CHLORIDE UNDER ALKALINE CONDITIONS. NOVEL ALKYLIDENIMINO PARA-SUBSTITUTED-PHENYL PHOSPHOCHLORIDATES AND ANALOGOUS THIOPHOSPHOROCHLORIDATES ARE ALSO DISCLOSED.
IN WHICH X IS OXYGEN OR SULFUR; Y IS OXYGEN OR SULFUR; R IS ALKYL; R1 IS ALKYL; R2 IS ALKYL OR ALKOXY AND R3 IS (1) PHENYL, OR (2) MONO-, DI OR TRI-DUBSTITUTED PHENYL WHEREIN THE SUBSTITUENT IS (A) NITRO OR (B) HALOGEN, AND THEIR USE AS INSECTICIDES, AND ACARICIDES ARE DISCLOSED. ALSO, THE INTERMEDIATES FOR PREPARING THE COMPOUNDS AND A METHOD FOR PREPARING THE INTERMEDIATES ARE DISCLOSED.
Abstract:
PESTICIDAL COMPOUNDS CLASSED AS PHENYL- AND SUBSTITUTED-PHENYLGLYOXYLONITRILE OXIMINO PHOPHATES AND PHOSPHONATES. TYPICAL OF THE COMPOUNDS PROVIDED ARE THE O,O-DIALKYL O-(4 - HALOPHENYLGLYOXYLONITRILE OXIMINO) PHOSPHATES AND THE S-ALKYL O-(4-HALOPHENYLGLOYOXYLONITRILE) ALKYLPHOSPHONATES. THE INVENTION FURTHER PROVIDES METHODS USING SAID COMPOUNDS S PESTIVIDES, AS WELL AS PESTICIDAL COMPOSITIONS CONTAINING THE NEW COMPOUNDS AND PESTICIDAL CRRIES THEREFOR.
Abstract:
A highly efficient and safe N-cyanation and N-phosphorylation reagent for the de novo synthesis of pharmaceutically acceptable cyclocreatine and salts was achieved using trichloroacetonitrile in lieu of highly toxic cyanogen bromide (CNBr) for generating the required cyclocreatine (CCr) intermediates, followed by highly effective N-phosphorylation through pH control using phosphoryl chloride with high conversion to the corresponding cyclocreatine phosphate (CCrP) targets. A continuous flow reactor system was engineered to improve the efficiency of the process and deliver a product with improved yield, safety, and cost efficiency.
Abstract:
This invention relates to compounds that inhibit creatine transport and/or creatine kinase, pharmaceutical compositions including such compounds, and methods of utilizing such compounds and compositions for the treatment of cancer.
Abstract:
The invention pertain to novel photoacid generator compounds of the formula I, II or III wherein R1 is for example C1-C18alkylsulfonyl or phenylsulfonyl, phenyl-C1-C3alkylsulfonyl, naphthylsulfonyl, anthracylsulfonyl or phenanthrylsulfonyl, all optionally substituted, or R1 is a group X1, X2 and X3 independently of each other are O or S; R′1, is e.g. phenylenedisulfonyl, naphthylenedisulfonyl, diphenylenedisulfonyl, or oxydiphenylenedisulfonyl, all optionally substituted; R2 is halogen or C1-C10haloalkyl; X is halogen; Ar1 is for example biphenylyl or fluorenyl, or is substituted naphthyl; Ar′1 is heteroarylene, optionally substituted; R8, R9, R10 and R11 for example are C1-C6alkyl which is unsubstituted or substituted by halogen; or R8, R9 and R10 are phenyl which is unsubstituted or substituted by C1-C4alkyl or halogen; or R10 and R11 together are 1,2-phenylene or C2-C6alkylene which is unsubstituted or substituted by C1-C4alkyl or halogen.
Abstract:
Radically photopolymerizable compositions comprising (a) at least one ethylenically unsaturated photopolymerizable compound; (b) as photoinitiator, at least one compound of formulae (I, II, III, IV, V and/or VI), wherein m is 0 or 1; n is 0, 1, 2 or 3; x is 1 or 2; R1 is inter alia phenyl, naphthyl, anthracyl or phenanthryl, a heteroaryl radical, C2-C12alkenyl, C4-C8cycloalkenyl, or C6-C12bicycloalkenyl; R′1 is inter alia C2-C12alkylene, or phenylene; R2 has one of the meanings of R1 or inter alia is phenyl; y is 1 or 2; R3 if x is 1 inter alia is C1-C18alkylsulfonyl, or phenyl-C1-C3alkylsulfonyl, R3 if x is 2, is for example C2-C12alkylenedisulfonyl; R4 and R5 inter alia are hydrogen, halogen, or C1-C8alkyl; R6, R7, R8 inter alia are hydrogen, R26Y—, or phenyl; R9 inter alia is C5-C8cycloalkyl, or phenyl; A is for example —S—, —O—, or —NR10—; Q is C1-C8-alkylene optionally interrupted by —O—; X is —O— or —NR9—; R10 inter alia is hydrogen, or phenyl; and (c) at least one coinitiator; are especially suitable for the preparation of color filter systems.
Abstract:
Oximinophosphoric acid derivatives of the formula ##STR1## where R.sup.1, R.sup.2 and R.sup.3 have the meanings given in the description, processes for their preparation, and their use for controlling pests.
Abstract:
MONO OR POLY HALO-SUBSTITUTED OXIME CARBAMATES AND PHOSPHATES CHARACTERIZED BY EITHER ONE OF THE FOLLOWING FORMULAS:
R-C6H4-C(-CF3)=N-O-C(=Y)-N(-R'')-R", OR R-C6H4-C(-CF3)=
N-O-P(=Y)(-R'')-O-R"
WHERE X IS HALOGEN.
R-C6H4-CO-C(-X)3
WHEREIN R IS ONE SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, METHYL, ISOPROPYL, ETHYL, TRIFLUOROMETHYL, FLUORINE, CHLORINE, BROMINE, METHOXY, METHYLTHIO, NITRO, DIMETHYLAMINO, ETHOXY, AND ISOPROPYLOXY; R'' IS ONE SELECTED FROM THE GROUP CONSISTING OF OR", C1 TO C6 ALKYL, C6 TO C10 ARYL, SUBSTITUTED ALKYL OR ARYL WHEREIN SAID SUBSTITUENT GROUPS ARE SELECTED FROM THE GROUP CONSISTING OF METHYL, ETHYL, TRIFLUOROMETHYL, FLUORINE, CHLORINE, BROMINE; R" IS C1 TO C6 ALKYL, C6 TO C10 ARYL, SUBSTITUTED ALKYL, ARYL WHEREIN THE SUBSTITUENTS ARE THE SAME AS THAT ENUMERATED FOR R''; Y IS S OR O. THESE COMPOUNDS HAVE SHOWN ACTIVITY AS INSECTICIDES. SUCH OXIME CARBAMATES AND PHOSPHATES CAN BE PREPARED FROM KETONES SUCH AS THOSE OF THE FORMULA: