Examples of 'tetrazolyl' in a sentence
Meaning of "tetrazolyl"
Tetrazolyl (noun) - a chemical compound containing a tetrazole ring structure
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- A radical derived from a tetrazole
How to use "tetrazolyl" in a sentence
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tetrazolyl
An example of such a heteroaromatic group is a tetrazolyl group.
Synthesis of tetrazolyl derivatives.
Additional preferred examples are furanyl and tetrazolyl.
In certain embodiments, each tetrazolyl group is unsubstituted.
Suitable examples of the aromatic heterocyclic group in the above substituents include triazolyl and tetrazolyl.
Is a carboxy group or a tetrazolyl group.
Phenyl, tetrazolyl and pyridyl are preferred.
A process for the production of tetrazolyl compounds.
The tetrazolyl oxime derivative or salt thereof according to claim 1, wherein Y represents a methyl group.
Is also preferably a tetrazolyl group.
Scheme IV shows the replacement of one of the carboxy groups with tetrazolyl.
The acidic group may be carboxyl, tetrazolyl or carboxamidotetrazolyl.
Field of the invention This invention relates to a technology for producing tetrazolyl compounds.
A suitable carboxylic acid bioisostere is selected from tetrazolyl and oxadiazolonyl . X is preferably a carboxylic acid.
In a further embodiment X represents a group selected from oxadiazolyl and tetrazolyl.
See also
Finally, Y may be a tetrazolyl functional group.
Preparation of the compounds of the formula I in which A represents tetrazolyl.
Is tetrazolyl group, a carboxyl group ; or an amide or an ester thereof ;.
A suitable carboxylic acid bioisostere is selected from tetrazolyl and oxadiazolonyl.
Tetrazolyl group of general formula,.
R ² is preferably an acid group especially tetrazolyl or carboxy.
Tetrazolyl oxime derivative, salt thereof, and plant disease control agent.
Examples include oxazolyl, oxadiazolyl and tetrazolyl rings.
In some embodiments, the tetrazolyl group is further substituted at either the 1 or 5 position resepectively.
A composition according to claim 1, wherein the heterocyclic residue is tetrazolyl.
R2 is preferably a tetrazolyl residue.
Is independently selected from the group consisting of, triazolyl and tetrazolyl.
Ring A is a pyrimidinyl group, a pyridyl group, a tetrazolyl group or an oxadiazolyl group ;.
A suitable 5-membered heteroaromatic ring containing four nitrogen atoms is tetrazolyl.
Number 5 corresponds to L1 being tetrazolyl salified by triphenyl methyl.
Further examples of monocyclic heterocyclic aromatic rings include pyrazinyl, tetrazolyl or imidazolyl.
A tetrazolyl group, a 5-membered heterocyclic group.
Scheme 3 shows two alternative methods for the preparation of the tetrazolyl derivatives.
Tetrazolyl is preferably 5-tetrazolyl.
The compounds can be the free acid, a salt form, or the tetrazolyl or aldehyde analog.
As R3, a tetrazolyl group is preferable.
In certain embodiments Het is optionally-substituted tetrazolyl group.
A suitable substituent for N-linked tetrazolyl is perhaloC1-6alkyl.
A group of preferred compounds are those wherein R3 is selected from COOH or tetrazolyl.
Moreover, R3 may be a tetrazolyl group.
A method according to claim 14, wherein the heterocyclic residue is tetrazolyl.
Patent Document 5 discloses a plant disease control agent containing a tetrazolyl oxime derivatives and salts thereof.
A compound as claimed in claim 9 wherein Q1 is an optionally substituted oxadiazolyl or tetrazolyl radical.
In a preferred embodiment R1 is a tetrazolyl group.
Exemplary 5-membered heteroaryl groups containing four heteroatoms include, without limitation, tetrazolyl.
R3 represents a carboxyl group or a tetrazolyl group ;.
Examples of cyclic aromatic radicals include aryl, indolyl, thienyl, furyl, pyrrolyl, triazolyl and tetrazolyl.
D is a pyrimidinyl group, a pyridyl group, a phenyl group, a pyrimidinyloxy group, a tetrazolyl group, or an oxazolidinyl group ;.
In another embodiment, R2 is independently selected from the group consisting of, triazolyl and tetrazolyl.
In some embodiments Het is optionally-substituted tetrazolyl group.
