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One-pot facile conversion of the acetates of Baylis–Hillman adducts into substituted fused pyrimidones in aqueous media
A facile, one-pot convenient transformation of the acetates of Baylis–Hillman adducts into fused pyrimidones, i.e. 3-substituted-1,5-diazabicyclo(4.4.0)deca-2,5,7,9-tetraen-4-ones via reaction with 2-aminopyridine in environmentally friendly aqueous media is described. A facile, one-pot convenient t...
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Published in: | Tetrahedron letters 2002-06, Vol.43 (24), p.4301-4303 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A facile, one-pot convenient transformation of the acetates of Baylis–Hillman adducts into fused pyrimidones, i.e. 3-substituted-1,5-diazabicyclo(4.4.0)deca-2,5,7,9-tetraen-4-ones via reaction with 2-aminopyridine in environmentally friendly aqueous media is described.
A facile, one-pot convenient transformation of the acetates of Baylis–Hillman adducts into fused pyrimidones, i.e. 3-substituted-1,5-diazabicyclo(4.4.0)deca-2,5,7,9-tetraen-4-ones via reaction with 2-aminopyridine in aqueous media is described. |
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ISSN: | 0040-4039 1873-3581 |
DOI: | 10.1016/S0040-4039(02)00802-X |