Diastereoselective synthesis of novel heterocyclic scaffolds through tandem Petasis 3-component/intramolecular Diels-Alder and ROM-RCM reactions
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- Diastereoselective_synthesis_of_novel_heterocyclic_scaffolds_through_tandem_Petasis_3-component:intramolecular_Diels-Alder_and_ROM-RCM_reactions_2017_accepted
Accepted author manuscript, 482 KB, PDF document
A high-yielding, stereoselective and extraordinarily complexity-generating Petasis 3-component/intramolecular Diels–Alder reaction has been developed. In combination with ROM–RCM, rapid access to complex sp3-rich heterocyclic scaffolds amenable to subsequent functionalization and library synthesis is provided.
| Original language | English |
|---|---|
| Journal | Chemical Communications |
| Volume | 53 |
| Issue number | 68 |
| Pages (from-to) | 9410-9413 |
| ISSN | 1359-7345 |
| DOIs | |
| Publication status | Published - 2017 |
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