Journal
ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 9, Issue 20, Pages 6895-6898Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c1ob05887h
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Funding
- National Science Foundation of China [20872043, 21072069, 21002036]
- National Basic Research Program of China [2011CB808600]
- Program for Changjiang Scholars and Inovation Research Team in University [IRT0953]
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Palladium-catalyzed C-H acetoxylation reactions of 2-methoxyimino-2-aryl-acetates and acetamides have been developed. These transformations feature excellent regioselectivity, wide substrate scope, and moderate to good yields. The product can be easily converted into naturally unprecedented alpha-amino acids in excellent yields.
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