4.8 Article

Allyl sulfides are privileged substrates in aqueous cross-metathesis: Application to site-selective protein modification

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 130, Issue 30, Pages 9642-+

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja8026168

Keywords

-

Funding

  1. BBSRC [BB/E004350/1] Funding Source: UKRI
  2. EPSRC [EP/E000614/1] Funding Source: UKRI
  3. Biotechnology and Biological Sciences Research Council [EGA17763, BB/E004350/1] Funding Source: Medline
  4. Biotechnology and Biological Sciences Research Council [BB/C510824/1, BB/E004350/1, EGA17763] Funding Source: researchfish
  5. Engineering and Physical Sciences Research Council [GR/T26542/01, EP/D023335/1, EP/E000614/1, EP/D023343/1] Funding Source: researchfish

Ask authors/readers for more resources

Allyl sulfides undergo efficient cross-metathesis in aqueous media with Hoveyda-Grubbs second generation catalyst 1. The high reactivity of allyl sulfides in cross-metathesis was exploited in the first examples of cross-metathesis on a protein surface. S-Allylcysteine was incorporated chemically into the protein, providing the requisite allyl sulfide handle. Preliminary efforts to genetically incorporate S-allylcysteine into proteins are also reported.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available