| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5264253 | Tetrahedron Letters | 2014 | 5 Pages |
Abstract
In Pd-catalyzed arylboronic acid addition to aryl aldehydes, the expected carbinol or asymmetrical ether can be obtained as the major product by altering aqueous solvent composition. Exploiting this methodology with 2-formylbiphenyls as reaction partner, a fluorene scaffold can be readily constructed in two steps.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Tuluma Das, Amarnath Chakraborty, Amitabha Sarkar,