Thionyl chloride/triethylamine : a powerful reagent for regiospecific and stereospecific formation of olefins from β-hydroxyselenides. stereospecific deoxygenation of di- and trisubstituted epoxides a [C.C] connective route to di-, tri- and tetrasubstituted olefins.

Tetrahedron Letters

Volumn 17, Issue 41, 1976, Pages 3743-3746

  Remion J ^a   Krief, A ^a  

^a UNIVERSITY OF NAMUR   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0000270134     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)93098-3     Document Type: Article

References (11)

1. New regiospecific routes to olefins from β-hydroxy selenides
2. Selenium stablized anions. Conversion of ?-hydroxy selenides into olefins
3. Regiospecific synthesis of αβ-unsaturated epoxides
4. A new method for the synthesis of olefins via β-hydroxyalkyl phenyl sulfides
5. The preparation of seleniranium and selenirenium ions