Abstract
Further examples of the occurrence of intramolecular translactonization during condensation of 4-hydroxy-6-methyl-2H-pyran-2-one, 1, or 4-hydroxycoumarin, 4, with carbonyl compounds are desoribed. The structure of previously misassigned products 6a,b is proven by NMR techniques. Application of the HETNOE method to the distinction between structures 9 and 10 is demonstrated. © 1987.
Original language | English |
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Pages (from-to) | 2381-2387 |
Journal | Tetrahedron |
Volume | 43 |
Issue number | 10 |
DOIs | |
Publication status | Published - 1 Jan 1987 |