1990
DOI: 10.1002/chin.199031173
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ChemInform Abstract: A Simple and General One‐Pot Synthesis of Some 2H‐Pyran‐2‐ones and Fused Pyran‐2‐ones.

Abstract: Dicarbonyl compounds such as (I) and (VII) react with N‐acylglycines such as (III) and (VI) and one‐carbon synthons such as (II) and (VIII) to yield pyranones (IV) and (V).

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Cited by 8 publications
(10 citation statements)
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“…Diels-Alder reactions between a set of fused pyran-2-ones 1 [35][36][37] and ethyl vinyl ether (2; see Scheme 1) were initially conducted in closed vessels (10 cm 3 ) under microwave irradiation [38][39][40][41][42][43][44][45][46] at 120°C, with the addition of DABCO as the catalyst. We found that such conditions (analogous to those used previously) [31,32] were not adequate to achieve quantitative conversion into the products 5; indeed, the only way to achieve this was to apply higher reaction temperatures (140-180°C).…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Diels-Alder reactions between a set of fused pyran-2-ones 1 [35][36][37] and ethyl vinyl ether (2; see Scheme 1) were initially conducted in closed vessels (10 cm 3 ) under microwave irradiation [38][39][40][41][42][43][44][45][46] at 120°C, with the addition of DABCO as the catalyst. We found that such conditions (analogous to those used previously) [31,32] were not adequate to achieve quantitative conversion into the products 5; indeed, the only way to achieve this was to apply higher reaction temperatures (140-180°C).…”
Section: Resultsmentioning
confidence: 99%
“…1 H NMR spectra were recorded at 29°C with a Bruker (Rheinstetten, Germany) Avance DPX 300 spectrometer at 300 MHz or Bruker Avance III spectrometer at 500 MHz, using TMS as an internal standard. 13 [35][36][37]. All other reagents and solvents were used as received from commercial suppliers.…”
Section: Methodsmentioning
confidence: 99%
“…[30][31][32] In conclusion, 6-acetyl-5-(1-pyrrolyl)-4-methyl-2-phenylthieno[2,3-d]pyrimidine 4 has been shown to be a useful building block for the synthesis of some new Schiff's bases 6a-f, chalcones 15a-k, pyridines 21a-f, pyridin-2(1H)-ones 26a,b and 2H-pyran-2-one derivatives 30a-c.…”
Section: Scheme IIImentioning
confidence: 99%
“…Due to the wide applicability of 2H-pyran-2-ones, a straightforward one-pot synthesis starting from the simple commercially available compounds was desired [19][20][21].…”
Section: Introductionmentioning
confidence: 99%