Abstract:
The present invention relates to cyanoenamine derivatives, their process of preparation, intermediate compounds, their use as fungicide active agents, particularly in the form of fungicide compositions, and methods for the control of phytopathogenic fungi, notably of plants and in material protecion, using these compounds or compositions.
Abstract:
Novel substituted chromone compounds which are intermediates for chromone compounds useful as bactericides and herbicides. Specifically, substituted chromone compounds represented by general formula (1) wherein R represents hydrogen, C1-6 alkyl, etc.; R represents hydrogen or C1-6 alkyl; R represents halogeno, etc.; R represents hydrogen, halogeno, etc.; R represents hydrogen, C1-6 alkyl, etc.; X represents oxygen or sulfur; and A represents nitro, etc.
Abstract translation:新颖的取代色酮化合物,其是用作色酮化合物的中间体,可用作杀菌剂和除草剂。 具体来说,由通式(1)表示的取代的色酮化合物,其中R 1表示氢,C 1-6烷基等; R 2表示氢或C 1-6烷基; R 3表示卤素等。 R 4表示氢,卤素等; R 5表示氢,C 1-6烷基等; X表示氧或硫; A代表硝基等
Abstract:
The present invention relates to new classes of odorous tetrahydropyran-4-ol derivatives of formula X and/or alkene derivatives thereof of formula Y1 and Y2 which are useful as fragrance or flavor materials in particular in providing camphoraceous, woody, earthy, and/or patchouli-like notes to perfume, aroma or deodorizing/masking compositions. The present invention also relates to fragrance, flavor and/or deodorizing/masking compositions comprising said new classes of odorous tetrahydropyran-4-ol derivatives and/or alkene derivatives thereof.
Abstract:
Cyclohexanedione compounds of Formula (I) wherein R 1 is methyl, ethyl, n -propyl, iso -propyl, cyclopropyl, halomethyl, haloethyl, halogen, vinyl, ethynyl, methoxy, ethoxy, halomethoxy or haloethoxy, R 2 and R 3 are, independently hydrogen, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, C 2 -C 6 alkenyl, C 2 -C 6 haloalkenyl, C 2 -C 6 alkynyl, C 3 -C 6 alkenyloxy, C 3 -C 6 haloalkenyloxy, C 3 -C 6 alkynyloxy, C 3 -C 6 cycloalkyl, C 1 -C 6 alkylthio, C 1 -C 6 alkylsulfinyl, C 1 -C 6 alkylsulfonyl, C 1 -C 6 alkylsulfonyloxy, C 1 -C 6 haloalkylsulfonyloxy, cyano, nitro, phenyl, phenyl substituted by C 1 -C 4 alkyl, C 1 -C 3 Cahaloalkyl, C 1 -C 3 alkoxy, C 1 -C 3 haloalkoxy, cyano, nitro, halogen, C 1 -C 3 alkylthio, C 1 -C 3 alkylsulfιnyl or C 1 -C 3 alkylsulfonyl, or heteroaryl or heteroaryl substituted by C 1 -C 3 Calkyl, d.Cahaloalkyl, C 1 -C 3 aIkoxy, C 1 -C 3 haloalkoxy, cyano, nitro, halogen, C 1 -C 3 alkylthio, C 1 -C 3 alkylsulfinyl or C 1 -C 3 alkylsulfonyl, R 4 is hydrogen, methyl, ethyl, n -propyl, iso -propyl, halomethyl, haloethyl, halogen, vinyl, ethynyl, methoxy, ethoxy, halomethoxy or haloethoxy, X is O, S, S(O) or S(O) 2 , R 5 is hydrogen or methyl, R 6 is hydrogen, methyl or ethyl, or forms a double bond, which links the carbon atom, to which R 6 is attached, with the adjacent carbon atom of R 7 or R 8 , R 7 and R 8 are independently of each other C 1 -C 5 alkylene, which is unsubstituted or substituted by methyl or ethyl, or C 2 -C 5 alkenylene, which is unsubstituted or substituted by methyl or ethyl, and G is hydrogen, an alkali metal, alkaline earth metal, sulfoniυm, ammonium or a latentiating group, are suitable for use as herbicides.
Abstract:
An improved process for preparing a saccharinic acid or lactone is disclosed that utilizes the well-known Amadori rearrangement reaction. The synthesis utilizes protected or unprotected sugars or their analogues as starting materials, and reagents not previously utilized to afford increased product yields in decreased reaction time.
Abstract:
Nitrogenous ambruticines of the general formula (I) wherein R is N(CH3)3+, NH(CH¿3?)2?+, NH¿2CH3+ ou NH¿3?+, and their pharmaceutically and agrochemically acceptable salts. The invention concerns new nitrogenous ambruticines, a process for obtaining them from Sorangium (Polyangium) cellulosum So ce 10 and their use as fungicides in mammals and plants.
Abstract:
The present invention is directed to heterocycloalkenyl derivatives, pharmaceutical compositions containing them and their use in the treatment of disorders and conditions modulated by the GPR120 and / or GPR40 receptors. 5 More particularly, the compounds of the present invention are agonists of GPR120 and / or GPR40, useful in the treatment of, for example, obesity, Type II Diabetes Mellitus, dyslipidemia, etc.
Abstract:
The present invention relates to novel compounds with a variety of therapeutic uses, more particularly novel substituted cyclic alkylidene compounds that are particularly useful for selective estrogen receptor modulation. Formula (I) including salts, solvates, and pharmacologically functional derivatives thereof wherein R is OH; each of R and R independently are selected from OH, alkyl, or halogen; each of p and q independently are selected from 0, 1, or 2; R is -(Y)z-R ; z is 0 or 1; Y is -C=C- or CR =CR -; X is -(CH2)n- where n is 0, 1, 2, or 3, -C(R )2-, -O-,or -S-.