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High pressure Diels–Alder reactions of (+)-nopadiene with cycloalkenones

✍ Scribed by Lucio Minuti; Aldo Taticchi; Assunta Marrocchi; Alessandra Broggi; Eszter Gacs-Baitz

Book ID
108283745
Publisher
Elsevier Science
Year
2004
Tongue
English
Weight
291 KB
Volume
15
Category
Article
ISSN
0957-4166

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High-Pressure-Promoted Diels−Alder Reactions between Cycloalkenones and 3-Methylsulfanylfuran and 3-Phenylsulfanylfuran
✍ H. Surya Prakash Rao; Rajappa Murali; Aldo Taticchi; Hans W. Scheeren 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 271 KB 👁 2 views

3-Methylsulfanylfuran and 3-phenylsulfanylfuran were found to undergo facile, regioselective and stereoselective Diels-Alder (DA) cycloaddition to a variety of cycloalkenones under high pressure to give the corresponding ringannulated 7-oxabicyclo[2.2.