Highly efficient molybdenum-based catalysts for enantioselective alkene metathesis
Steven J. Malcolmson,
Simon J. Meek,
Elizabeth S. Sattely,
Richard R. Schrock and
Amir H. Hoveyda ()
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Steven J. Malcolmson: Merkert Chemistry Center, Boston College, Chestnut Hill, Massachusetts 02467, USA
Simon J. Meek: Merkert Chemistry Center, Boston College, Chestnut Hill, Massachusetts 02467, USA
Elizabeth S. Sattely: Merkert Chemistry Center, Boston College, Chestnut Hill, Massachusetts 02467, USA
Richard R. Schrock: Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA
Amir H. Hoveyda: Merkert Chemistry Center, Boston College, Chestnut Hill, Massachusetts 02467, USA
Nature, 2008, vol. 456, issue 7224, 933-937
Abstract:
A new chiral catalyst Alkene metathesis (also called olefin metathesis or transalkylidenation) is an organic reaction widely used to synthesize products including medicines, polymers and fuels. Its importance was recognized in 2005, when Yves Chauvin, Robert Grubbs and Richard Schrock shared the Nobel prize for work on metathesis. A new class of molybdenum-based chiral catalyst, capable of initiating alkene metathesis with exceptional efficiency and enantioselectivity, is reported in this issue. The new catalysts bear a stereogenic metal centre and carry only monodentate ligands. Their effectiveness was demonstrated in an enantioselective synthesis of the Aspidosperma alkaloid, quebrachamine, via a metathesis reaction that cannot be promoted by any of the previously reported catalysts.
Date: 2008
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DOI: 10.1038/nature07594
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