Journal
ORGANIC LETTERS
Volume 13, Issue 9, Pages 2492-2494Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol2007428
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Funding
- National Institutes of Health [CA042056]
- Skaggs Institute for Chemical Biology
- Novartis
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An examination of the scope of the inverse electron demand Diels-Alder reactions of the parent unsubstituted 1,2,3-triazine is described including the first report of its unique capabilities for participating in previously unexplored [4 + 2] cycloaddition reactions with heterodienophiles.
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