Publication details

Rearrangement of fused tetracyclic heterocycles induced by alkyl halides and formation of a new type of "proton sponge"

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Authors

PÍŽOVÁ Hana MAN Stanislav TARABA Jan POTÁČEK Milan

Year of publication 2009
Type Article in Periodical
Magazine / Source Tetrahedron
MU Faculty or unit

Faculty of Science

Citation
Doi http://dx.doi.org/10.1016/j.tet.2008.11.057
Field Organic chemistry
Keywords tetracyclic fused heteocycles; rearrangement; alkyl halides initiation; proton sponge;
Description Intramolecular criss-cross cycloaddition of 3-substituted symmetrical homoallenyl azines 2 by heating in xylene lead to interesting fused heterocyclic systems consisting of four five-membered rings with two nitrogen atoms in the skeleton 3. These compounds 3 were found to be sensitive to attack by alkyl halides. Their presence, depending on the reaction conditions, resulted in a new type of rearrangement leading to compounds 4 and 5, respectively. With an excess of alkyl halide and in the presence of NaBH3CN a new structure 6 with signs of the molecule corresponding a proton sponge moiety was created. The scope of the rearrangement and reaction products structure was investigated.
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