STERIC EFFECTS IN GOMBERG REACTION

[1] ANGOOD DR, 1952, J CHEM SOC, P2094

[2] AUGOOD DR, 1957, CHEM REVS, V57, P183

[3] FREE RADICAL AROMATIC SUBSTITUTION .4. THE REACTION OF ACYL PEROXIDES WITH BENZOTRIHALIDES [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1954, 76 (18) : 4543 - 4546

[4] NEW PRODUCTS FROM THE REACTION OF BENZOYL PEROXIDE WITH BENZENE [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1958, 80 (17) : 4742 - 4743

[5] A QUANTITATIVE STUDY OF THE ORIENTING INFLUENCE OF THE NITRO GROUP IN THE FORMATION OF NITROBIPHENYLS BY REACTION OF NITROBENZENE WITH N-NITROSOACETANILIDE, WITH BENZOYL PEROXIDE, AND WITH BENZENEDIAZONIUM CHLORIDE AND ALKALI [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1951, 73 (04) : 1442 - 1445

[6] The synthesis of biaryl compounds by means of the diazo reaction [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1924, 46 : 2339 - 2343

[7] HEY, 1951, J CHEM SOC, P2892

[8] HEY DH, 1959, THEORETICAL ORGANIC, P257

[9] HEY DH, 1953, DISCUSS FARADAY SOC, V14, P216

[10] HUISGEN, 1950, ANNALEN, V566, P162

[1] ANGOOD DR, 1952, J CHEM SOC, P2094

[2] AUGOOD DR, 1957, CHEM REVS, V57, P183

[3] FREE RADICAL AROMATIC SUBSTITUTION .4. THE REACTION OF ACYL PEROXIDES WITH BENZOTRIHALIDES [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1954, 76 (18) : 4543 - 4546

[4] NEW PRODUCTS FROM THE REACTION OF BENZOYL PEROXIDE WITH BENZENE [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1958, 80 (17) : 4742 - 4743

[5] A QUANTITATIVE STUDY OF THE ORIENTING INFLUENCE OF THE NITRO GROUP IN THE FORMATION OF NITROBIPHENYLS BY REACTION OF NITROBENZENE WITH N-NITROSOACETANILIDE, WITH BENZOYL PEROXIDE, AND WITH BENZENEDIAZONIUM CHLORIDE AND ALKALI [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1951, 73 (04) : 1442 - 1445

[6] The synthesis of biaryl compounds by means of the diazo reaction [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1924, 46 : 2339 - 2343

[7] HEY, 1951, J CHEM SOC, P2892

[8] HEY DH, 1959, THEORETICAL ORGANIC, P257

[9] HEY DH, 1953, DISCUSS FARADAY SOC, V14, P216

[10] HUISGEN, 1950, ANNALEN, V566, P162