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The Diels−Alder Reactions of Quinone Imine Ketals: A Versatile Synthesis of Highly Substituted 5-Methoxyindoles

✍ Scribed by Banfield, Scott C.; England, Dylan B.; Kerr, Michael A.

Book ID
121432427
Publisher
American Chemical Society
Year
2001
Tongue
English
Weight
48 KB
Volume
3
Category
Article
ISSN
1523-7060

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📜 SIMILAR VOLUMES

ChemInform Abstract: The Diels—Alder Rea
ChemInform Abstract: The Diels—Alder Reactions of Quinone Imine Ketals: A Versatile Synthesis of Highly Substituted 5-Methoxyindoles.
✍ Scott C. Banfield; Dylan B. England; Michael A. Kerr 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 36 KB 👁 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

The Diels—Alder Reactions of Quinone Imi
The Diels—Alder Reactions of Quinone Imine Ketals.
✍ Scott C. Banfield; Michael A. Kerr 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 242 KB 👁 2 views

## Abstract For Abstract see ChemInform Abstract in Full Text.

ChemInform Abstract: The High Pressure D
ChemInform Abstract: The High Pressure Diels-Alder Reactions of Quinone-mono-ketals.
✍ E. R. JARVO; S. R. BOOTHROYD; M. A. KERR 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 2 views

The High Pressure Diels-Alder Reactions of Quinone-mono-ketals. -Simple quinone-mono-ketals react with nonactivated dienes at high pressure to yield the corresponding adducts. Treatment of these adducts with catalytic acid forms the aromatized products, i.e. the annulated benzenes or naphthalenes.