Imperial Chemical Industries Limited

Zeneca Limited

Syngenta Corporation

Syngenta Participations Ag

Syngenta Crop Protection, Inc.

Sandoz Gmbh

Other

Paul A Worthington

Margaret C Shephard

William G Rathmell

Keith P Parry

Patrick J Crowley

John M Clough

Daniel Stierli

Vivienne M Anthony

Paul J De Fraine

Fredrik Cederbaum

Ian R Matthews

Michael B Gravestock

Balasubramanyan Sugavanam

Gordon Richard Munns

Charles Adam Russell

Don R Baker

Peter Maienfisch

Harald Walter

Jerome Yves Cassayre

Christopher John Urch

Alfred Glyn Williams

Michael J Bushell

Louis-Pierre Molleyres

Kurt Nebel

Nigel James Willetts

Brian K Snell

David John Hughes

Nicholas Phillip Mulholland

Alaric James Avery

Eric Daniel Clarke

Antoine Daina

Richard Spurring Roberts

John Dalziel

James Edward Peace

Brian L Pilkington

Mark Richard Ashton

Thomas Stephen Coulter

Thomas Pitterna

Roger Salmon

Anthony Cornelius O'Sullivan

Alain De Mesmaeker

Raymond Vincent Jones

Olivier Loiseleur

Paul John deFraine

David J Collins

William Guy Whittingham

Michael J Robson

John Benjamin Taylor

Karl J Fisher

Michael Charles Standen

David A Griffin

David John Ritchie

Torsten Luksch

Vladimir Bobosik

David Bartholomew

Ian Henry Aspinall

Timothy Lewis

Anthony M Skidmore

Johannes Paul Pachlatko

Diana M Gatehouse

Anthony F Marchington

Paul DeFraine

John J Taylor

Julie Forrester

Kevin Robert Lawson

Leslie Francis May

Ian T Streeting, Deceased

Mario Jorg

Balsubramanyan Sugavanam

Insecticidal, acaricidal, nematicidal or molluscicidal compounds of formula (I) wherein Y is a single bond, C&#x2550;O, C&#x2550;S or S(O)where q is 0, 1 or 2; and R, R, R, R, R, Rare Rare as defined in the claims or salts or N-oxides thereof, processes for preparing them and compositions containing them.

Spiroindolinepiperidine derivatives

Compounds of the formula I in which the substituents are as defined in claimare suitable for use as microbiocides.

Iminipyridine derivatives and their uses as microbiocides

A compound of formula (I) wherein R1 to R4 are, for example, each hydrogen, R5 is pyridyl, which has two or more substituents selected, for example, from halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy, and cyano; R6 is, for example, hydrogen; R7 is, for example, hydrogen, cyano, hydroxyl, formyl, C1-C4-alkyl, C1-C4-alkoxy, C2-C4-alkenyl, or C2-C4-alkynyl; and A1 to A5 are, independently selected, from, for example, N, and C&#x2014;H; and its use as a pesticidal agent. 

Pesticidal compounds

The present invention provides a compound of formula (I) wherein Ris of sub-formula (a) or (b) and wherein the other substituents are as defined in the specification. The compounds of formula (I) are potentially useful as herbicides. 

Herbicidal 5H-quinoxaline-6-one derivatives detailed description

Compounds of the formula (I) in which the substituents are as defined in claimare suitable for use as microbiocides. Formula (I), wherein X is oxygen or sulfur; A is a 5- or 6-membered heterocyclic ring containing one to three heteroatoms, each independently selected from oxygen, nitrogen and sulphur, or a phenyl ring; the heterocyclic ring or the phenyl being substituted by the groups R, Rand R; R, Rand Rare each, independently, hydrogen, halogen, cyano, nitro, Calky, Chalogenalkyl, Chalogenalkoxy, Calkoxy(C)alkyl or Chalogenalkoxy(C)alkyl, provided that at least one of R, Rand Ris not hydrogen; B is a phenyl, naphthyl or quinolinyl group, which is substituted by one or more substituents R. 

Microbiocides

The present invention relates to 6,6-dioxo-6-thia-1,4-diaza-naphthalene derivatives of formula (I) where R, R, R, R, Rand Rare as defined in claim; or a salt or N-oxide thereof. Furthermore, the present invention relates to processes and intermediates for making compounds of formula (I), to herbicidal compositions comprising compounds of formula (I) and to methods of using compounds of formula (I) to control plant growth. 

6, 6-dioxo-6-thia-1, 4-diaza-naphthalenes as herbicides

Compounds of the formula (I) in which the substituents are as defined in claimare suitable for use as microbiocides. 

Compounds of the formula (I), which are suitable for use as microbiocides, and in which A is A, or A is A, or A is A, or A is Aand B is a phenyl, naphthyl or quinolinyl group. 

Ethenyl carboxamide derivatives useful as microbiocides

Fungicidal compounds of the general formula (I): wherein X and Y are independently H, halo, Calkyl, Ccycloalkyl, Calkenyl, Calkynyl, Calkoxy, Calkylthio, nitro, amino, mono- or di-(C)alkylamino, mono- or di-(C)alkenylamino, mono- or di-(C)alkynylamino, formylamino, Calkyl(formyl)amino, Calkylcarbonylamino, Calkyl(Calkylcarbonyl)amino, cyano, formyl, Calkylcarbonyl, Calkoxycarbonyl, aminocarbonyl, mono- or di-(C)alkylaminocarbonyl, carboxy, Calkylcarbonyloxy, aryl(C)alkylcarbonyloxy, Calkylsulphinyl, Calkylsulphonyl, Calkylsulphonyloxy, aryl, heteroaryl, aryloxy, arylthio, heteroaryloxy or heteroarylthio wherein any of the foregoing alkyl, cycloalkyl, alkenyl, alkynyl, aryl, heteroaryl, groups or moieties are optionally substituted; Ris phenyl, cyano, Calkyl, Calkenyl or Calkynyl in which the alkyl, alkenyl and alkynyl groups are optionally substituted on their terminal carbon atom with one, two or three halogen atoms, with a cyano group, with a Calkylcarbonyl group, with a Calkoxycarbonyl group or with a hydroxy group, or Ris alkoxyalkyl, alkylthioalkyl, alkylsulphinylalkyl or alkylsulphonylalkyl in which the total number of carbon atoms is 2 or 3; Ris H, Calkyl, Calkoxymethyl or benzyloxymethyl in which the phenyl ring of the benzyl moiety is optionally substituted with Calkoxy; Rand Rare independently H, Calkyl, Calkenyl or Calkynyl provided that both are not H and that when both are other than H their combined total of carbon atoms does not exceed 4, or Rand Rjoin with the carbon atom to which they are attached to form a 3 or 4 membered carbocyclic ring optionally containing one O, S or N atom and optionally substituted with halo or Calkyl; and Ris halo, Calkyl or Ccycloalkyl in which the alkyl or cycloalkyl group is optionally substituted with halo, hydroxy, Calkoxy, Calkylthio, cyano, Calkylcarbonyloxy, aminocarbonyloxy, mono- or di(C)alkylaminocarbonyloxy, or tri(C)alkylsilyloxy. The compounds and compositions containing them are especially useful for combating fungal infections of plants.

Pyridyloxyalkanoic acid amide derivatives useful as fungicides

A compound of the following formula ##STR1## wherein M is an alkali metal or alkaline earth metal atom and a process for the preparation of the compound is provided.

Process for the preparation of 2-(pyrid-2-yloxymethyl)phenylacetates as

Process for the preparation of 2-(6-substituted pyrid-2-yloxymethyl)

Aralkyoxy alkoximino derivatives and their use as fungicides

The invention provides a process for the preparation of a compound of the general formula (I): ##STR1## wherein X, Y and R.sup.1 to R.sup.7 are as defined. In the process, the olefinic analog of the compound of general formula (I) is treated with a halogen-bearing compound in the presence of metallic zinc.

Process for cylopropane derivatives

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Maidenhead, United Kingdom

Paul A Worthington