Synthetic Strategies Towards Naturally Occurring Tetronic Acids
✍ Scribed by Alexandros L. Zografos; Dimitris Georgiadis
- Publisher
- John Wiley and Sons
- Year
- 2007
- Weight
- 11 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Abstract
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## Abstract magnified image A synthetic approach involving a solubilizing protecting group strategy is described to generate pyrido[2,3‐__d__:6,5‐__d__′]dipyrimidine‐2,4,6,8‐tetrones functionalized at positions 1 and 9 with alkylamine substitutents. J. Heterocyclic Chem., **46**, 79 (2009).
## Abstract Various synthetic approaches were employed to prepare 2‐benzyl‐2‐hydroxybenzofuran‐3(2__H__)‐one (**8**), the prototype of naturally occurring auronols. While the base‐induced ring transformation of 3‐hydroxyflavanone (**2**) as well as the hydration of 2‐benzylidenebenzofuran‐3(2__H__)