ChemInform Abstract: Indium(III) Chloride Catalyzed Mukaiyama—Michael Addition: Synthesis of 2,6-anti-Tetrahydropyrans.
✍ Scribed by Sin-Siu Chua; Anita Alni; Li-Ting Jocelyn Chan; Motoki Yamane; Teck-Peng Loh
- Publisher
- John Wiley and Sons
- Year
- 2011
- Weight
- 28 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0931-7597
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## Abstract Highly efficient and regioselective methods for the synthesis of 1,5‐ and 1,8‐naphthyridines (II), (V) catalyzed by I~2~ and InCl~3~, resp., are developed.
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Stereocontrolled Synthesis of Cyclic Ethers by Intramolecular Hetero-Michael Addition. Part 5. Synthesis of All Diastereoisomers of 2,3,5,6-Tetrasubstituted Tetrahydropyrans. -The intramolecular hetero-Michael addition of 7-hydroxy-4-(benzoyloxy)-2,3-unsaturated esters is found to be an excellent wa