Formal total synthesis of triptolide
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Authors
Miller, Natalie
Willis, Anthony
Sherburn, Michael
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Royal Society of Chemistry
Abstract
A new approach to the medicinally-important natural product triptolide is significantly shorter than previous syntheses, highly convergent and avoids the use of protecting groups; key features include two Diels-Alder reactions and a new deoxygenative aromatisation process.
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Chemical Communications
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Restricted until
2037-12-31
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