Journal
ORGANIC LETTERS
Volume 16, Issue 10, Pages 2720-2723Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol501006t
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- DST New Delhi
- UGC
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A facile preparation of benz-annulated heterocycles were achieved at rt involving a Lewis acid/Bronsted acid mediated annulation of heterocycles using 2,5-dimethoxytetrahydrofuran as a four-carbon synthon. The benz-/naphth-annulation was found to be successful with electron-rich arenes as well.
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