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Recent News and Articles on the Keywords: new + synthesis + oxidation  Related to the article below (Last Update: 8/5/2008)

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Source: Google News

Insertion of specific bases during DNA synthesis past the oxidation-damaged base 8-oxodG -
S Shibutani, M Takeshita, AP Grollman - Nature, 1991 - nature.com
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8 ... Department of Pharmacological Sciences, State University of New York at ...

Revised effective ionic radii and systematic studies of interatomic distances in halides and … -
RD Shannon - Crystal Physics, Diffraction, Theoretical and General …, 1976 - Blackwell Synergy
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Steroids. LXXIII. 1a The Direct Oppenauer Oxidation of Steroidal Formate Esters. A New Synthesis of …
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The Organometallic Chemistry of the Transition Metals -
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[CITATION] … and Characterization of New Vanadium Phosphorus Oxide Catalysts for Partial n-Butane Oxidation to …
NH Batis, H Batis, A Ghorbel, JC Vedrine, JC Volta - J. Catal, 1991

CHOP induces death by promoting protein synthesis and oxidation in the stressed endoplasmic … -
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... To measure translation of new proteins within the membrane fraction ... 20 mM NEM to
block further protein synthesis and prevent ex vivo protein oxidation. ...

Source: Google Scholar

New oxidation methods streamline synthesis of important compounds

CHAMPAIGN, Ill. — One of the fundamental challenges facing organic synthesis in the 21st century is the need to significantly increase the efficiency with which carbon frameworks can be constructed and functionalized. Chemists at the University of Illinois are helping to meet this challenge by developing a class of carbon-hydrogen catalysts that are highly selective, reactive and tolerant of other functionality.

The catalysts also offer a new strategy for streamlining the synthesis of important compounds, including drugs and pharmaceuticals, by avoiding the functional group manipulations required for working with oxidized materials.

“We are creating a toolbox of catalytic reactions that allow us to go directly from a carbon-hydrogen bond to a carbon-oxygen bond or to a carbon-nitrogen bond,” said M. Christina White, a professor of chemistry at Illinois. “By offering fewer steps, fewer functional group manipulations and higher yields, this toolbox will change the way chemists make molecules.”
Currently, chemists must make molecules by beginning with something that is already oxidized. But, having to start with that functionality means it must be carried – and protected – throughout the entire synthetic sequence. And that costs reagents, time, money and manpower, in addition to being inherently inefficient.

“Unlike standard synthetic methods, we don’t have to carry the functionality throughout the entire sequence,” White said. “Instead, we carry latent functionality as a carbon-hydrogen bond. Then, at a late stage in the synthesis, we remove the hydrogen and replace it with oxygen or nitrogen – right where we need it for the next chemical reaction.”

In the June 13 issue of the Journal of the American Chemical Society, White and graduate student Kenneth J. Fraunhoffer describe the catalytic pathway they used to synthesize a derivative of the chemotherapeutic reagent acosamine. They were able to eliminate all of the functional group manipulations and cut by one-half the number of steps required, while maintaining the same purity and yield.

White has also used her catalyst to streamline the synthesis of a peptidase inhibitor drug candidate, a nucleotide-sugar L-galactose, and is currently working on the antibiotic erythromycin A.

White’s research is funded by the Henry Dreyfus Foundation, the A.P. Sloan Foundation, the University of Illinois, Merck Research Laboratories, the National Institutes of Health and the National Science Foundation.

Editor’s note: To reach M. Christina White, call 217-333-6173; e-mail: white@scs.uiuc.edu

To view or subscribe to the RSS feed for Science News at Illinois, please go to: http://webtools.uiuc.edu/rssManager/608/rss.xml.
 
 
 
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