Journal
CHEMICAL COMMUNICATIONS
Volume -, Issue 18, Pages 1974-1976Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b601433j
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The substituted tricyclic pyrano[ 2,3-e] isoindolin-3-ones 2 and 3, as the core structure of stachybotrin A, B, and C (1a-c), have been regioselectively synthesized for the first time by a short route which involved Mannich reaction and Claisen rearrangement.
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