Syngenta Corporation

Syngenta Crop Protection, Inc.

Syngenta Participations Ag

David John Hughes

Eric Daniel Clarke

Patrick J Crowley

Christopher John Mathews

André Jeanguenat

Olivier Loiseleur

Russell Colin Viner

William Guy Whittingham

John C Williams

Stephen Christopher Smith

Susan Patricia Barnett

Nigel John Barnes

Sarah Armstrong

Torquil Eoghan Macleod Fraser

Alan John Whittle

James Edward Peace

Peter Maienfisch

Jerome Yves Cassayre

Paul A Worthington

Stephan Trah

Roger Salmon

Fredrik Cederbaum

Christopher John Urch

Louis-Pierre Molleyres

Richard Spurring Roberts

Charles Adam Russell

Mark Richard Ashton

Brian Leslie Pilkington

Thomas Stephen Coulter

Andrew Edmunds

Michel Muehlebach

Peter Renold

André Stoller

Roger Graham Hall

Anthony Cornelius O'Sullivan

Jean Wenger

Sally Elizabeth Russell

William Roderick Mound

Patricia Durieux

Suzanna Jane Riley

Joan Pilkington, Legal Representative

Stephen Paul Heaney

Joseph John Swanborough

Paul Anthony Worthington

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 formula (I), wherein the substituents are as defined in claim, and the agrochemically acceptable salts and all stereoisomers and tautomeric forms of the compounds of formula I can be used as agrochemical active ingredients and can be prepared in a manner known per se. 

Pesticides containing a bicyclic bisamide structure

Compounds of formula I wherein the substituents are as defined in claim, and the agrochemically acceptable salts and all stereoisomers and tautomeric forms of the compounds of formula I can be used as agrochemical active ingredients and can be prepared in a manner known per se.

Insecticides

Compounds of the formula (I) in which Z, is an oxygen atom; or a sulfur atom; Zis an oxygen atom; or a sulfur atom; R, is an aryl or heteroaryl group, which is unsubstituted or substituted; Ris hydrogen; or an organic substituent; Ris hydrogen; or an organic substituent; Ris hydrogen; or an organic substituent; or Rand R, taken together, form, together with the nitrogen atom, to which they are attached, a ring, which is unsubstituted or substituted; Ris hydrogen; or an unsubstituted or substituted alkyl group; or forms, taken together with Ror with a monovalent substituent attached to that atom of R, via which atom Ris directly connected with the carbon atom, shown in the formula I, which carries R, one additional bond; Rand R, taken together, form, together with the two carbon atoms, shown in the formula I, to which atoms they are attached, a bicyclic ring system, which ring system is carbocyclic or heterocyclic, which ring system is substituted, in the manner shown in the formula I, by the four substituents &#x2014;N(R2)-C(&#x2550;Z1)-R, &#x2014;C(&#x2550;Z2)-N(R3)-R4, Rand R8, and which ring system is optionally further substituted; and Ris hydrogen; or an unsubstituted or substituted alkyl group; or forms, taken together with Ror with a monovalent substituent attached to that atom of R, via which atom Ris directly connected with the carbon atom, shown in the formula I, which carries R8, one additional bond, and, where appropriate, tautomers thereof, in each case in free form or in salt form, can be used as agrochemical active ingredients and can be prepared in a manner known per se. 

A compound of formula (I) wherein G is either (i) or (ii), where Mor Mis bonded to A; n is 0 or 1; when G is (i), D is S, NR, CR&#x2550;CR, CR&#x2550;N, CR&#x2550;N(O), N&#x2550;CRor N(O)&#x2550;CR; when G is (ii), D is S or NR; E is N, N-oxide or CR; Mis OC(&#x2550;Y), N(R)C(&#x2550;Y), N&#x2550;C(OR), N&#x2550;C(SR) or N&#x2550;C(NRR) where O or N is the atom of attachment to the ring containing D and E; Mis N&#x2014;C(&#x2550;Y) where N is the atom of attachment to the ring containing D and E; Y is O, S or NR; J is N or CR; and A, R, R, R, R, R, R, R, R, R, R, R, R, R, Rand Rare each certain organic or inorganic groups. These compounds are useful in fungicidal, insecticidal, acaricidal, molluscicidal and hematicidal compositions.

Pesticidal indazole or benzotriazole derivatives

A compound of formula (I), where A is optionally substituted alkylene, alkenylene, alkynylene, cycloalkylene, alkylenoxy, oxy(C )alkylene, alkylenthio, thio(C )alkylene, C alkylenamino, amino(C )alkylene, &lsqb;C alkyleneoxy(C )alkylene&rsqb;, &lsqb;C alkylenethio(C )alkylene&rsqb;, &lsqb; alkylenesulfinyl(C )alkylene&rsqb;, &lsqb;C alkylenesulfonyl(C )alkylene&rsqb; or &lsqb;C alkyleneamino(C )alkylene&rsqb;; provided that A is not CH or CH O; B is N,N-oxide or CR ; Y is O, S or NR ; Z is O, S or NR ; and R , R , R , R , R , R , R , R , R , R are specified radicals; compositions containing them; process for making them; and their use as insecticides or fungicides.

Isothiazole derivatives and their use as pesticides

Benzazoles: benzoxazole, benzthiazole and benzimidazole derivatives

Growing community of inventors

Bracknell, United Kingdom

David John Hughes