SYED ASIM ALI, MD
Psychiatric at Whitehorse Mercerville Rd, Trenton, NJ

6753429, Jun 22, 2004

Aug 29, 2001

09/941812

George Theodoridis - Princeton NJ
Edward Barron - Trenton NJ
Daniel H. Cohen - Princeton NJ
Ellen M. Crawford - Jackson NJ
Thomas G. Cullen - Andover MA
Hongyan Qi - Plainsboro NJ
Elizabeth Rowley - Kendall Park NJ
Syed F. Ali - Yardville NJ
Walter H. Yeager - Yardley PA
Christina B. Duggan - Plainsboro NJ

FMC Corporation - Philadelphia PA

C07D24104

544395, 546206, 549443, 564299, 564308, 564341, 564347, 514277, 514278, 514649, 514657

Compounds of formula I: wherein A, B, D, and R are as defined herein and their agriculturally acceptable salts are disclosed as effective insecticides. In addition, compositions comprising an insecticidally effective amount of a compound of Formula I in admixture with at least one agriculturally acceptable extender or adjuvant and methods of controlling insects comprising applying said compositions to locus on crops where control is desired are disclosed. It is emphasized that this abstract is provided to comply with the rules requiring an abstract that will allow a searcher or other reader to quickly ascertain the subject matter of the technical disclosure. It is submitted with the understanding that it will not be used to interpret or limit the scope or meaning of the claims (see 37 C. F. R. 1. 72(b)).

6214845, Apr 10, 2001

Sep 2, 1999

9/388592

Ian R. Silverman - Moorestown NJ
Daniel H. Cohen - Princeton NJ
John W. Lyga - Basking Ridge NJ
Steven W. Szczepanski - Walnut Creek CA
Syed F. Ali - Yardville NJ
Thomas G. Cullen - Milltown NJ
Robert N. Henrie - Pennington NJ
Clinton J. Peake - Trenton NJ

FMC Corporation - Philadelphia PA

A01N 4340, A01N 4354, C07D40110, C07D41710

514326

Compounds of the following structure, the corresponding N-oxides and agriculturally acceptable salts, are disclosed as effective insecticides: ##STR1## in which U is --(CH. sub. 2). sub. n --; Q is hydroxy; R is ##STR2## in which V, W, Y, and Z are each hydrogen; X is a five- or six-membered heterocycle; optionally substituted with halogen, cyano, alkyl, haloalkyl, alkoxy, haloalkoxy, alkoxyalkyl, haloalkoxyalkyl, or aminocarbonyl; and the heterocycle is optionally connected to the phenyl ring through a --O--, --S--, --(CH. sub. 2). sub. p, --C(O)--, or --O--(CR. sup. 3 R. sup. 4). sub. q linkage; R. sup. 1 and R. sup. 2 are independently selected from phenyl or pyridyl substituted with haloalkyl or haloalkoxy; R. sup. 3 and R. sup. 4 are independently selected from hydrogen and methyl; n and p are independently 1, 2, or 3; and q is 1 or 2; with the proviso that at least one of R. sup. 1 and R. sup. 2 is substituted in the para position; no more than two of R. sup. 3 and R. sup.

H2079, Dec 4, 2001

Jan 9, 1997

8/780371

Ian R. Silverman - Moorestown NJ
Syed F. Ali - Yardville NJ
Daniel H. Cohen - Princeton NJ
John W. Lyga - Basking Ridge NJ
Kirk A. Simmons - Newtown PA
Thomas G. Cullen - Milltown NJ

FMC Corporation - Philadelphia PA

C07D29500, C07D40300, C07D24104, C07D24102

544358

Compounds of the following structure are disclosed as effective insecticides: ##STR1## in which: A and B are independently lower alkyl; U is lower alkylidene, lower alkenylidene, or CH--Z, where Z is hydrogen, lower alkyl, lower cycloalkyl, or phenyl; R is phenyl or a dibenzocyclo(C. sub. 5-8)alkyl, each optionally substituted, or ##STR2## where R. sup. 3 and R. sup. 4 are independently selected from phenyl, optionally substituted with, halogen, lower alkyl, lower haloalkyl, lower alkoxy, lower haloalkoxy, lower alkenyl, or phenyl; R. sup. 1 is selected from a variety of substituents, including 3-R. sup. 2, where R. sup. 2 is ##STR3## where D, E, and G are hydrogen, hydroxy, halogen, cyano, hydroxy, lower alkyl, lower haloalkyl, lower alkoxy, nitro, lower haloalkylsuffonyloxy, lower alkylcarboxylato, lower alkylcarbonylamino, lower alkylcarbonyl, lower alkoxycarbonyl, arylcarbonylamino; D and E taken together may form the group --O(CH. sub. 2)O--; J is hydrogen or lower alkyl; m is 2 or 3, n is 1, 2, or 3; and halogen is chlorine, bromine, or fluorine.

6184234, Feb 6, 2001

Oct 7, 1999

9/414375

Ian R. Silverman - Moorestown NJ
Daniel H. Cohen - Princeton NJ
John W. Lyga - Basking Ridge NJ
Steven W. Szczepanski - Walnut Creek CA
Syed F. Ali - Yardville NJ
Thomas G. Cullen - Milltown NJ
Robert N. Henrie - Pennington NJ
Clinton J. Peake - Trenton NJ

FMC Corporation - Philadelphia PA

A01N 4340, A01N 4354, C07D40510

514321

Compounds of the following structure, the corresponding N-oxides and agriculturally acceptable salts thereof, are disclosed as effective insecticides: ##STR1## wherein U is --(CH. sub. 2). sub. n --; Q is hydroxy; and R is: ##STR2## and wherein V, W, Y, and Z are each hydrogen; X is a five- or six-membered heterocycle; optionally substituted with bromine, chlorine, fluorine, cyano, alkyl, haloalkyl, alkoxy, haloalkoxy, alkoxyalkyl, haloalkoxyalkyl, or aminocarbonyl; and the heterocycle is optionally connected to the phenyl ring through a --O--, --S--, --(CH. sub. 2). sub. p, --C(O)--, or --O--(CR. sup. 3 R. sup. 4). sub. q linkage; R. sup. 1 and R. sup. 2 are independently selected from phenyl or pyridyl substituted with pentahalothio, haloalkylthio, haloalkylsulfinyl, or haloalkylsulfonyl; phenyl substituted with --OC(M). sub. 2 O--, where M is bromine, chorine or fluorine, to provide a dihalobenzodioxolyl fused ring; or pyridyl substituted with --OC(M). sub.

6030987, Feb 29, 2000

Aug 11, 1998

8/981456

Ian R. Silverman - Moorestown NJ
Daniel H. Cohen - Princeton NJ
John W. Lyga - Basking Ridge NJ
Steven W. Szczepanski - Morrisville PA
Syed F. Ali - Yardville NJ
Thomas G. Cullen - Milltown NJ
Robert N. Henrie - East Windsor NJ
Clinton J. Peake - Trenton NJ

FMC Corporation - Philadelphia PA

A01N 4340, A01N 4354, C07D40110, C07D41710

514326

Compounds of structure (I) ##STR1## the corresponding N-oxides and agriculturally acceptable salts are disclosed as effective insecticides. In said formula, U is --(CH. sub. 2)n--; Q is hydroxy, R is formula (II) ##STR2## in which V, W, Y and Z are hydrogen; X is a five- or six-membered heterocycle optionally substituted; and the heterocycle is optionally connected to the phenyl ring through a --O--, --S-- --CH. sub. 2)p--, or --O(CR. sup. 3 R. sup. 4)q linkage; R. sup. 1 and R. sup. 2 are independently selected from phenyl or pyridyl substituted with haloalkyl or haloalkoxy; R. sup. 3, R. sup. 4, n, p, and 1 are as defined in the specification.

7247756, Jul 24, 2007

Jan 29, 2003

10/353471

George Theodoridis - Princeton NJ, US
Edward Barron - Trenton NJ, US
Daniel H. Cohen - Princeton NJ, US
Ellen M. Crawford - Jackson NJ, US
Thomas G. Cullen - Andover MA, US
Hongyan Qi - Plainsboro NJ, US
Elizabeth Rowley - Kendall Park NJ, US
Syed F. Ali - Yardville NJ, US
Walter H. Yeager - Yardley PA, US
Christina B. Duggan - Plainsboro NJ, US

Bayer CropScience AG - Monheim

C07C 43/20

568634

Compounds of formula I:.