“…6,7 The Baylis-Hillman reaction has proved to be a powerful tool for C-C bond-forming reactions, which are also atom economical, green and simple reaction and provide densely functionalised molecules, The Baylis-Hillman adducts have become valuable sources for making cyclic frameworks containing heteroatoms. [8][9][10][11] In pursuit of the interest in the synthesis of heterocyclic molecules, [12][13][14][15] we now report a onepot, microwave-assisted fast protocol for facile transformation of the Baylis-Hillman adducts into bicyclic heterocyclic frameworks containing a pyrimidone moiety.…”
Two types of fused pyrimidones, 3-substituted-7-chloro-4H-pyrimido[1,2-b]pyridazin-4-ones and 6-substituted-5H-thiazolo-[3,2-a]pyrimidin-5-ones were easily prepared from Baylis-Hillman adduct acetates under microwave irritation in high yields.
“…6,7 The Baylis-Hillman reaction has proved to be a powerful tool for C-C bond-forming reactions, which are also atom economical, green and simple reaction and provide densely functionalised molecules, The Baylis-Hillman adducts have become valuable sources for making cyclic frameworks containing heteroatoms. [8][9][10][11] In pursuit of the interest in the synthesis of heterocyclic molecules, [12][13][14][15] we now report a onepot, microwave-assisted fast protocol for facile transformation of the Baylis-Hillman adducts into bicyclic heterocyclic frameworks containing a pyrimidone moiety.…”
Two types of fused pyrimidones, 3-substituted-7-chloro-4H-pyrimido[1,2-b]pyridazin-4-ones and 6-substituted-5H-thiazolo-[3,2-a]pyrimidin-5-ones were easily prepared from Baylis-Hillman adduct acetates under microwave irritation in high yields.
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