Montedison S.p.a.

Isagro S.p.a.

Ministero Dell 'universita'e Della Ricerca Scientifica E Technologica

Isagro Ricerca S.r.l.

Presidenza Del Consiglio Dei Ministri

Istituto Guido Donegani

Other

Ministero Dell'universita E Della Ricerca Scientifica E Tecnologica

Agrimont S.r.l.

Ministero Dell'universita' E Della Ricerca Scientifica E

Ministero Delli `universita` E Della Ricerca Scientifica E Tecnologica

Ministero Dell 'universita' E Dell Ricerca Scientifica E Tecnologica

Minestero Dell' Universita 'e Della Ricerca Scientifica E Technologica

Presidenza Del Consiglio Dei Ministri Ufficio Del Ministro Per Il Coordinamento Delle Iniziative Per La Ricerca Scientifica E Tecnologica

Belchim Crop Protection Luxembourg S.a.r.l.

Luigi Mirenna

Carlo Garavaglia

Giovanni Camaggi

Lucio Filippini

Marilena Gusmeroli

Franco Gozzo

Roberto Colle

Raul Riva

Giuseppina Ratti

Giampaolo Zanardi

Silvia Mormile

Luigi Garlaschelli

Laura Colombo

Giovanni Meazza

Isabella Venturini

Alexia Elmini

Angela Zagni

Luigi Capuzzi

Franco Bettarini

Ernesto Signorini

Simone Lorusso

Giorgio Pirali

Ottorino Palla

Giorgio Cassani

Giovanni Confalonieri

Augusto Menconi

Francesco Corda

Silvia Spera

Giorgio E Borgonovi

Mario Ferri

Anacleto Dal Moro

Mirella Cecere

Nunzio Andriollo

Marco Vincenti

Daniela Tolentino

Walter Visentin

Alessandro Ciapessoni

Antonio Malandra

Vincenzo Mendillo

Samuele Osti

Ramona Gironda

Nicola Stramacchia

Claude Delestre

Guido Zini

Giorgio Borgonovi

Mixtures are described comprising two or more compounds selected from at least two of the following groups: i) salicylic acid and/or its functional analogous products (ESA), ii) promoting compounds (PRO) and iii) modulating compounds (MOD), and their use for stimulating the natural defense systems of plants and for inducing resistance in plants. The use is also described, of two or more compounds selected from at least two of the following groups: one or more compounds belonging to the ESA group and/or one or more compounds belonging to the PRO group and/or one or more compounds belonging to the MOD group, individually adopted by means of application programs which envisage alternating application, to stimulate the natural defense systems of plants and inducing resistance in plants.

Mixtures and methods for the induction of resistance in plants

Composition for controlling phytopathogens comprising compound of the formula: wherein:

Compositions based on cupric salts, cupric salts and their use for controlling phytopathogens

Organic compounds are described, which are capable of forming quaternary salts, quaternary salts thereof with a structure having general formula (I) and their use for the control of phytopathogen fungi. 

Organic derivatives, their salts and use for the control of phytopathogens

Compounds having general formula (I) are described, together with their use for the control of phytopathogenic fungi 

Thiazole derivatives with fungicidal activity

Dipeptide compounds having a high fungicidal activity and their agronomic use

When used in admixture with mancozeb, chlorothalonil, a copper salt, folpet, fluazinam or cymoxanil (this being possible for the latter to be used also together with one of the other five components), metalaxyl having a high R-enantiomer content of more than 70% by weight, or pure R-metalaxyl, exhibits a markedly increased fungicidal action against plant diseases as compared with a similar mixture in which metalaxyl is used in the form of the racemate.

Fungicidal compositions based on (N-phenylacetyl-N-2,6-XYLYL)methyl alaninate

This invention refers to new analogs of strobilurine, having the general formula (I): ##STR1## The compounds of formula (I) are endowed with good stability and high fungicidal activity against phytopathogenous fungi, combined with good selectivity for the vegetable it is designed to apply to.

Analogs of strobilurine having fungicidal properties, and their

Adjuvants for systemic fungicides in the form of a stable microemulsion comprise water, a mixture of methyl esters of fatty acids obtained by the transesterification of vegetable oils, an anionic surface-active agent, at least one non-ionic surface-active agent with an HLB of between 13-18 and a cloud point of &gt;65.degree. and at least one non-ionic surface-active agent with an HLB of between 10 and 12. These adjuvants, which can additionally contain conventional components and/or formulation additives, improve the activity of systemic fungicides belonging to different chemical groups.

Adjuvants for systemic fungicides, fungicidal compositions which contain

A description follows of oximic derivatives with a fungicide activity, for agricultural use, having the formula (I): ##STR1## wherein: A, B, D, are N, or .dbd.C--G;

Oximic derivatives with a fungicide activity

A description follows of benzophenones having an antifungal activity and responding to the general formula (I): ##STR1## wherein: R.sub.1 and R.sub.2, the same or different, represent C.sub.1 -C.sub.6 alkyl groups, C.sub.7 -C.sub.10 arylalkyl groups; or R.sub.1 and R.sub.2, considered jointly with N, represent a C.sub.3 -C.sub.8 heterocyclic group or a C.sub.2 -C.sub.7 heterocyclic group containing a second hetero-atom selected from O and S, said heterocyclic groups being optionally subsituted with one or more C.sub.1 -C.sub.4 alkyl groups;

Benzophenones having an antifungal activity

The ethylamino phenyl ethers of the invention and compositions thereof are endowed with high activities as inhibitors of the growth of several species of pathogen fungi and are applied to plants or to plant parts and are effective in preventing the diseases caused by pathogen fungi, such as, e.g., those belonging to Erysiphe and Helminthosporium genera.

Ethylamino phenyl ethers having antifungal activity

Aryl-propyl-aminic compounds having the following formula ##STR1## have high activity and are useful in the agricultural field as fungicides.

Aryl-propyl-amines endowed with antifungal activity

Compounds based on 3,4-diaryl-(5H)-furan-2-one, with fungicidal activity, having the general formula (I): ##STR1##

3,4-diaryl-5(H)-furan-2-one based compounds with fungicidal activity

Compounds based on derivatives of pyrrole[2,1-b]- and imidazo[2,1-b-]thiazoles, with a fungicidal activity, having the general formula (I): ##STR1##

Thiazole derivatives of alkoxyacrylates with a fungicidal activity

Compounds based on 2-thiazole-2-ylpyrrole, with a fungicidal activity, having the general formula (I): ##STR1##

Thiazolylpyrroles having a fungicidal activity

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Milan, Italy

Luigi Mirenna