A FREE RADICAL CHAIN MECHANISM FOR THE ISONITRILE - NITRILE REARRANGEMENT IN SOLUTION AND ITS INHIBITION.

DOI: 10.1016/S0040-4039(00)86223-1

Source and publish data:

Tetrahedron Letters p. 4671 - 4674 (1983)

Update date:2022-08-30

Topics:

Authors:

Meier, Michael

Ruechardt, Christoph

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Article abstract of DOI:10.1016/S0040-4039(00)86223-1

A large fraction of the isonitrile-nitrile rearrangement of t-alkyl isonitriles in solution follows a free radical chain mechanism of the addition-elimination type.

Full text of DOI:10.1016/S0040-4039(00)86223-1

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Article Doi

A FREE RADICAL CHAIN MECHANISM FOR THE ISONITRILE - NITRILE REARRANGEMENT IN SOLUTION AND ITS INHIBITION.

DOI: 10.1016/S0040-4039(00)86223-1

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(00)86223-1

Full text of DOI:10.1016/S0040-4039(00)86223-1

Products guided by the article

R&D Labs maybe for 20923-70-0

Relevant to this article

Synthesis of 4-substituted oxazolo[4,5-c]quinolines by direct reaction at the C-4 position of oxazoles

Synthesis, spectroscopic, and antimicrobial study of Ca(II), Fe(III), Pd(II), and Au(III) complexes of amoxicillin antibiotic drug

A novel high-stability Au(III)/Schiff-based catalyst for acetylene hydrochlorination reaction

Synthesis, crystal growth, structural, thermal and optical properties of naphthalene picrate an organic NLO material

Effect of linker length and composition on heterobivalent ligand-mediated receptor cross-talk between the A1 adenosine and β2 adrenergic receptors

Chlorotrimethylsilane: A powerful Lewis acidic catalyst in Michael-type Friedel-Crafts reactions of indoles and enones

Effect of linker length and composition on heterobivalent ligand-mediated receptor cross-talk between the A₁ adenosine and β₂ adrenergic receptors