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Olefin metathesis for chemical biology

Journal

CURRENT OPINION IN CHEMICAL BIOLOGY
Volume 12, Issue 6, Pages 767-773

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.cbpa.2008.09.022

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Funding

  1. NIH [GM044783]
  2. NSF

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Chemical biology relies on effective synthetic chemistry for building molecules to probe and modulate biological function. Olefin metathesis in organic solvents is a valuable addition to this armamentarium, and developments during the previous decade are enabling metathesis in aqueous solvents for the manipulation of biomolecules. Functional group-tolerant ruthenium metathesis catalysts modified with charged moieties or hydrophilic polymers are soluble and active in water, enabling ring-opening metathesis polymerization, cross metathesis, and ring-closing metathesis. Alternatively, conventional hydrophobic ruthenium complexes catalyze a similar array of metathesis reactions in mixtures of water and organic solvents. This strategy has enabled cross metathesis on the surface of a protein. Continuing developments in catalyst design and methodology will popularize the bioorthogonal reactivity of metathesis.

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