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Intramolecular Stereoselective Stetter Reaction Catalyzed by Benzaldehyde Lyase

Angewandte Chemie, 2021
AbstractThe reliable design and prediction of enzyme promiscuity to access transformations not observed in nature remains a long‐standing challenge. Herein, we present the first example of an intramolecular stereoselective Stetter reaction catalyzed by benzaldehyde lyase, guided by the rational structure screening of various ThDP‐dependent enzymes ...
Xiaoyang Chen   +6 more
openaire   +2 more sources

Intramolecular functionalisation by a methylene radical of a 1,2-diol and a vicinal amino alcohol: models for coenzyme B12-dependent diol dehydratase and ethanolamine ammonia lyase

Journal of the Chemical Society, Perkin Transactions 1, 2000
Coenzyme B12-dependent diol dehydratase converts 1,2-diols (e.g. propane-1,2-diol) into the corresponding aldehyde and water. The similar enzyme ethanolamine ammonia lyase transforms vicinal aminoalcohols (e.g. 2-aminoethanol) into the corresponding aldehyde and ammonia.
Andersen RJ   +3 more
openaire   +2 more sources

C−C Bond-Forming Lyases in Organic Synthesis

Chemical Reviews, 2011
Daniela Gamenara
exaly  

Synthetic and Therapeutic Applications of Ammonia-lyases and Aminomutases

Chemical Reviews, 2018
Fabio Parmeggiani   +2 more
exaly  

Immobilisation of hydroxynitrile lyases

Chemical Society Reviews, 2013
Ulf Hanefeld
exaly  

Pectate lyases: Their role in plants and importance in fruit ripening

Food Chemistry, 2020
Selman Uluisik, Graham B Seymour
exaly  

A Single Residue Influences the Reaction Mechanism of Ammonia Lyases and Mutases

Angewandte Chemie - International Edition, 2009
Sebastian Bartsch, Uwe T Bornscheuer
exaly  

Hydroxynitrile lyases: At the interface of biology and chemistry

Enzyme and Microbial Technology, 2005
Monica Sharma, Tek Chand Bhalla
exaly  

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