Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5223339 | Tetrahedron | 2009 | 5 Pages |
Abstract
Carbon nucleophiles generated by a non-nucleophilic base (LDA) were effectively trapped with di-tert-butyl dicarbonate (Boc-anhydride) to provide the corresponding tert-butyl aryl acetates, di-tert-butyl aryl malonates, unsymmetrical aryl malonates and tert-butyl benzoates in high yields. This reaction represents another useful way to prepare a variety of tert-butyl carboxylates and highlights the synthetic utility of di-tert-butyl dicarbonate as a versatile carboxylating reagent.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
John Kallikat Augustine, Y. Arthoba Naik, Veeramani Vairaperumal, Sharmila Narasimhan,