TY - JOUR
T1 - Direct formation of 3, 3, 6, 6-t etraaryl-1, 2-dioxans from 1, 1-diaryiethylenes and oxygen, catalysed by antimony(v) chloride
AU - Haynes, Richard K.
AU - Probert, Michael K.S.
AU - Wilmot, Ian D.
N1 - Funding Information:
We thank the Australian Research Grants Committee for financial support.
PY - 1978
Y1 - 1978
N2 - 1, 1-Diphenylethylene, 1, 1-di-p-tolylethylene, 1, 1-di-p-anisylethylene and 1, 1-di(p-t-butylphenyl)- ethylene are converted in high yields (80-90%) into the corresponding 3, 3, 6, 6-tetraaryl-1, 2-dioxans in the presence of oxygen and catalytic amounts of antimony(v) chloride in dichloromethane at -40° to - 78° under irradiation from a tungsten lamp.
AB - 1, 1-Diphenylethylene, 1, 1-di-p-tolylethylene, 1, 1-di-p-anisylethylene and 1, 1-di(p-t-butylphenyl)- ethylene are converted in high yields (80-90%) into the corresponding 3, 3, 6, 6-tetraaryl-1, 2-dioxans in the presence of oxygen and catalytic amounts of antimony(v) chloride in dichloromethane at -40° to - 78° under irradiation from a tungsten lamp.
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U2 - 10.1071/CH9781737
DO - 10.1071/CH9781737
M3 - Article
AN - SCOPUS:84970603427
SN - 0004-9425
VL - 31
SP - 1737
EP - 1746
JO - Australian Journal of Chemistry
JF - Australian Journal of Chemistry
IS - 8
ER -