Abstract
The development of an asymmetric route for the synthesis of α,β-butenolide building blocks, starting from commercially available d-mannitol, is described. The devised route was applied to a synthesis of the (S)-(-)-enantiomer of the antiviral natural product umbelactone, together with the construction of other synthetically useful lactone structures.
Originalsprog | Engelsk |
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Tidsskrift | SYNLETT: Accounts and Rapid Communications in Chemical Synthesis |
Udgave nummer | 4 |
Sider (fra-til) | 547-550 |
Antal sider | 4 |
ISSN | 0936-5214 |
DOI | |
Status | Udgivet - 2010 |
Udgivet eksternt | Ja |