The Reaction of 1, 2: 3, 4??Diepoxy??2, 3??dimethylbutane with Nucleophiles

…, T Wellauer, T Esser, URS Sequin

Index: Farkas, Frederic; Wellauer, Thomas; Esser, Thomas; Sequin, Urs Helvetica Chimica Acta, 1991 , vol. 74, # 7 p. 1511 - 1519

Full Text: HTML

Citation Number: 5

Abstract

Abstract To find out whether the 1, 4-addition to 1, 2: 3, 4-diepoxides, which so far has been observed only once, is of a more general character, we investigated the reaction of a variety of O-, C-, N-, and S-nucleophiles with the model compound 1, 2: 3, 4-diepoxy-2, 3- dimethylbutane (Scheme 4). In several cases, 1, 4-addition products could, indeed, be observed besides the expected 1, 2-adducts (Table).

Related Articles:

tert-Butylacetylene revisited. Improved synthesis. Methyl migration during bromination

[Collier,W.L.; Macomber,R.S. Journal of Organic Chemistry, 1973 , vol. 38, p. 1367 - 1369]

Studies of 1, 3-Dienes. II. Stereoisomerism of Bromides and Glycols Derived from 2, 3-Dimethyl-1, 3-butadiene1

[Sweeting; Johnson Journal of the American Chemical Society, 1946 , vol. 68, p. 1060]

Pure Liquids: Extended References

[Kogerman Chem. Zentralbl., 41 Nr. 3/4<1934>265 1935 , vol. 106, # I p. 2964]

More Articles...