Yayınlanmış 1 Ocak 2009
| Sürüm v1
Dergi makalesi
Açık
Regioselective synthesis of the 3,4-dihydrofuro[3,2-d]pyrimidin-2(1H)-one skeleton: a new class of compound
Oluşturanlar
- 1. Middle E Tech Univ, Dept Chem, TR-06531 Ankara, Turkey
- 2. Ataturk Univ, Dept Chem, TR-25240 Erzurum, Turkey
Açıklama
We hereby report the first preparation of the 3,4-dihydrofuro[3,2-d]pyrimidin-2(1H)-one skeleton formed by two controlled Curtius rearrangements of the corresponding acyl azides, prepared from 2-(2-methoxy-2-oxoethyl)furan-3-carboxylate via the hydrazide. Rearrangement of the acyl azides followed by trapping by nucleophiles and intramolecular trapping provided the target compounds. (C) 2009 Elsevier Ltd. All rights reserved.
Dosyalar
bib-ebb03716-256d-413a-8181-3a7ded12f1ab.txt
Dosyalar
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