TY - JOUR
T1 - TeCl4 in organic synthesis. Elimination reactions
AU - Albeck, Michael
AU - Tamary, Tova
PY - 1991/11/26
Y1 - 1991/11/26
N2 - TeCl4 has been shown to react smoothly with unsaturated or halogenated cyclohydrocarbons. With cyclohexene, alklcyclohexenes, halogenocyclohexenes, halogenocyclohexanes or unsaturated polycyclic compounds at elevated temperatures (ca 80°C), aromatization takes place as the only process, whereas at room temperature, addition products of halogenation or halogenotelluration are also formed. With conjugated dienes only chlorine-containing products are obtained with TeCl4, whereas dienes with separated double ponds undergo addition of TeCl4 to the double bond. An ionic pathway for the addition and aromatization reactions is suggested.
AB - TeCl4 has been shown to react smoothly with unsaturated or halogenated cyclohydrocarbons. With cyclohexene, alklcyclohexenes, halogenocyclohexenes, halogenocyclohexanes or unsaturated polycyclic compounds at elevated temperatures (ca 80°C), aromatization takes place as the only process, whereas at room temperature, addition products of halogenation or halogenotelluration are also formed. With conjugated dienes only chlorine-containing products are obtained with TeCl4, whereas dienes with separated double ponds undergo addition of TeCl4 to the double bond. An ionic pathway for the addition and aromatization reactions is suggested.
UR - http://www.scopus.com/inward/record.url?scp=0039641633&partnerID=8YFLogxK
U2 - 10.1016/0022-328x(91)86442-s
DO - 10.1016/0022-328x(91)86442-s
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AN - SCOPUS:0039641633
SN - 0022-328X
VL - 420
SP - 35
EP - 42
JO - Journal of Organometallic Chemistry
JF - Journal of Organometallic Chemistry
IS - 1
ER -