Ueber die Einwirkung von Salzsäure auf Arylazoacetaldoxime

Bamberger, Eug.; Frei, Johannes

doi:10.1002/cber.19020350114

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“…Bamberger and his students, for a period of eight years starting in 1894, condensed 1-nitro alkanes with aromatic diazonium salts (2,3,4,5,6). Similar work was done by Hantzsch and Kissel on nitroethane (11,12).…”

Section: Historical Surveymentioning

confidence: 85%

“…In the eighteen years that followed, Meyer and his students continued their study of the condensation of aromatic diazonium salts with 1-nitro alkanes (17), 3-nitropropene (1), and 1,3-dinitropropane (14). Duden in 1893 (9) reported a condensation with the potassium salt of dinitromethane.Bamberger and his students, for a period of eight years starting in 1894, condensed 1-nitro alkanes with aromatic diazonium salts (2,3,4,5,6). Similar work was done by Hantzsch and Kissel on nitroethane (11,12).Ponzio and collaborators studied condensations of aromatic diazonium salts with aromatic dinitromethanes (19, 20, 26), with diphenylnitromethane (25), and with trinitromethane (28, 29).…”

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confidence: 90%

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VII. THE CONDENSATION OF ARYL DIAZONIUM SALTS AND/OR HYDROXIDES WITH SECONDARY NITRO ALKANES¹

Feasley¹,

Degering²

1943

J. Org. Chem.

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Section: Historical Surveymentioning

confidence: 85%

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confidence: 90%

VII. THE CONDENSATION OF ARYL DIAZONIUM SALTS AND/OR HYDROXIDES WITH SECONDARY NITRO ALKANES¹

Feasley¹,

Degering²

1943

J. Org. Chem.

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The Coupling of Diazonium Salts with Aliphatic Carbon Atoms

Parmerter

2011

Organic Reactions

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A diazonium salt will couple with an aliphatic compound containing an activated carbon‐hydrogen bond. This discussion is limited to those reactions in which both the nitrogen atoms of the diazonium salts are retained in the resulting molecule. The discussion is further limited by the exclusion of coupling reactions, which occur with the elimination of a group from an activated methinyl compound, the Japp‐Klingemann reaction. These reactions are discussed in Chapter 2. Much of the early work with coupling was prompted by the desire to determine whether the products were of the azo or hydrazonestructure. It is difficult to establish the structures in such cases where the tautomeric forms are possible. It is generally considered that the hydrazone is the stable form.

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Nitronic acids and esters

Nielsen

Breuer

Aurich

1989

PATAI'S Chemistry of Functional Groups

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Ueber die Einwirkung von Salzsäure auf Arylazoacetaldoxime

Cited by 3 publications

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VII. THE CONDENSATION OF ARYL DIAZONIUM SALTS AND/OR HYDROXIDES WITH SECONDARY NITRO ALKANES¹

VII. THE CONDENSATION OF ARYL DIAZONIUM SALTS AND/OR HYDROXIDES WITH SECONDARY NITRO ALKANES¹

The Coupling of Diazonium Salts with Aliphatic Carbon Atoms

Nitronic acids and esters

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Ueber die Einwirkung von Salzsäure auf Arylazoacetaldoxime

Cited by 3 publications

References 0 publications

VII. THE CONDENSATION OF ARYL DIAZONIUM SALTS AND/OR HYDROXIDES WITH SECONDARY NITRO ALKANES1

VII. THE CONDENSATION OF ARYL DIAZONIUM SALTS AND/OR HYDROXIDES WITH SECONDARY NITRO ALKANES1

The Coupling of Diazonium Salts with Aliphatic Carbon Atoms

Nitronic acids and esters

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Product

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VII. THE CONDENSATION OF ARYL DIAZONIUM SALTS AND/OR HYDROXIDES WITH SECONDARY NITRO ALKANES¹

VII. THE CONDENSATION OF ARYL DIAZONIUM SALTS AND/OR HYDROXIDES WITH SECONDARY NITRO ALKANES¹