Substituted Phenyltetrazoles. Alkoxynitrophenyl-Tetrazoles and Alkoxyaminophenyltetrazoles

Wu, Du-Yung; Herbst, Robert

doi:10.1021/jo50009a006

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1953

2013

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Cited by 9 publications

(2 citation statements)

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“…The presence of a primary amine function on the phenyl group of the rearrangement product was rendered unlikely by the following experiment. In identical qualitative tests the rearrangement product, l-p-aminophenyl-5-methyltetrazole (16) Absorption Curves: A, 5-o-nitrophenylaminotetrazole (0.006 g. per 1. ); B, dinitro 5-phenylaminotetrazole (0.021 g. per 1.…”

Section: Experimental6•mentioning

confidence: 99%

The Synthesis of Certain 5-Aminotetrazole Derivatives. IV. The Rearrangement of Certain Monosubstituted 5-Aminotetrazole Derivatives

Garbrecht¹,

Herbst²

1953

J. Org. Chem.

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Section: Experimental6•mentioning

confidence: 99%

The Synthesis of Certain 5-Aminotetrazole Derivatives. IV. The Rearrangement of Certain Monosubstituted 5-Aminotetrazole Derivatives

Garbrecht¹,

Herbst²

1953

J. Org. Chem.

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“…Table II), yield 73 g. (80%). 2 All melting points are corrected. Analyses by Micro-Tech Laboratories, Skokie, Illinois.…”

Section: VImentioning

confidence: 99%

1,5-DISUBSTITUTED TETRAZOLES FROM 1-ACETYL-2-para-SUBSTITUTED BENZOYL HYDRAZINES AND p-NITROBENZENEDIAZONIUM CHLORIDE^*1

Horwitz¹,

Grakauskas²

1954

J. Org. Chem.

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Chlorosis induced by substituted benzoic acids and related compounds

Dimmock¹

1967

J Sci Food Agric

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A number of derivatives of 4-hydroxy-3-nitrobenzoic acid and 4-methoxy-3-nitrobenzoic acid and related compounds have been prepared, and their ability to produce chlorosis in six different species of plants has been examined. This series of compounds caused white and yellow areas to appear in the young tissues of the plants. A representative ester, ethyl-4-methoxy-3-nitrobenzoate, which caused this effect in barley was shown to affect the iron content and to reduce the quantity of pigments significantly. The structural requirements within this series of compounds for producing the type of chlorosis concerned are briefly discussed.

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Substituted Phenyltetrazoles. Alkoxynitrophenyl-Tetrazoles and Alkoxyaminophenyltetrazoles

Cited by 9 publications

References 10 publications

The Synthesis of Certain 5-Aminotetrazole Derivatives. IV. The Rearrangement of Certain Monosubstituted 5-Aminotetrazole Derivatives

The Synthesis of Certain 5-Aminotetrazole Derivatives. IV. The Rearrangement of Certain Monosubstituted 5-Aminotetrazole Derivatives

1,5-DISUBSTITUTED TETRAZOLES FROM 1-ACETYL-2-para-SUBSTITUTED BENZOYL HYDRAZINES AND p-NITROBENZENEDIAZONIUM CHLORIDE^*1

Chlorosis induced by substituted benzoic acids and related compounds

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Substituted Phenyltetrazoles. Alkoxynitrophenyl-Tetrazoles and Alkoxyaminophenyltetrazoles

Cited by 9 publications

References 10 publications

The Synthesis of Certain 5-Aminotetrazole Derivatives. IV. The Rearrangement of Certain Monosubstituted 5-Aminotetrazole Derivatives

The Synthesis of Certain 5-Aminotetrazole Derivatives. IV. The Rearrangement of Certain Monosubstituted 5-Aminotetrazole Derivatives

1,5-DISUBSTITUTED TETRAZOLES FROM 1-ACETYL-2-para-SUBSTITUTED BENZOYL HYDRAZINES AND p-NITROBENZENEDIAZONIUM CHLORIDE*1

Chlorosis induced by substituted benzoic acids and related compounds

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Product

Resources

About

1,5-DISUBSTITUTED TETRAZOLES FROM 1-ACETYL-2-para-SUBSTITUTED BENZOYL HYDRAZINES AND p-NITROBENZENEDIAZONIUM CHLORIDE^*1