The mild oxidation of nitrile oxides affords a convenient entry to nitrosocarbonyl intermediates, versatile tools in organic syntheses

Tetrahedron

Volumn 55, Issue 34, 1999, Pages 10497-10510

  Quadrelli, P ^a   Mella, M ^a   Gamba Invernizzi, A ^a   Caramella, P ^a  

^a UNIVERSITY OF PAVIA   (Italy)

Author keywords

Diels Alder reactions; N Oxides; Nitrile Oxides; Nitroso compounds; Solvents

Indexed keywords

ACETIC ACID ETHYL ESTER; ACETONE; ACETONITRILE; ALCOHOL; BENZENE; CARBON TETRACHLORIDE; CHLOROFORM; CYCLOHEXANE; DIMETHYL SULFOXIDE; DIOXANE; METHANOL; NITRILE; NITROSO DERIVATIVE; NITROSOCARBONYL DERIVATIVE; SOLVENT; TOLUENE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION KINETICS; CHEMICAL STRUCTURE; CYCLIZATION; HYDROLYSIS; OXIDATION; OXIDATION REDUCTION REACTION; PRIORITY JOURNAL; REACTION ANALYSIS; REDUCTION;

BETULACEAE;

EID: 0033588294     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(99)00574-8     Document Type: Article

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