ChemInform Abstract: Cycloaddition—Rearrangement Sequence of 2-Amido Substituted Furans as a Method of Synthesizing Hexahydroindolinones.
✍ Scribed by Albert Padwa; Michael A. Brodney; Kyosuke Satake; Christopher S. Straub
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 33 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
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📜 SIMILAR VOLUMES
Diels-Alder Reaction of 2-Amino-Substituted Furans as a Method for Preparing Substituted Anilines. -2-Amino substituted furans react with various dienophiles to intermediate (4 + 2) cycloadducts with high regioselectivity. The electron-withdrawing group is directed in all cases ortho to the amino g
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