|1.||Downs, Diana M: 8 articles (04/2015 - 01/2012)|
|2.||Lambrecht, Jennifer A: 5 articles (09/2014 - 01/2012)|
|3.||Flynn, Jeffrey M: 3 articles (08/2013 - 01/2012)|
|4.||Ernst, Dustin C: 2 articles (04/2015 - 09/2014)|
|5.||Lupilova, Nataliya: 2 articles (01/2014 - 07/2013)|
|6.||Kuhlmann, Katja: 2 articles (01/2014 - 07/2013)|
|7.||Müller, Alexandra: 2 articles (01/2014 - 07/2013)|
|8.||Tittmann, Kai: 1 article (12/2014)|
|9.||Li, Guoqing: 1 article (10/2014)|
|10.||Yang, Chun-Kai: 1 article (10/2014)|
04/01/2015 - "The reported activity of RidA and the consequences encountered in vivo when RidA is absent have challenged fundamental assumptions in enzymology, biochemistry and cell metabolism regarding the fate of transiently generated reactive enamine intermediates. "
10/01/2014 - "The dguB gene encodes a putative enamine/imine deaminase of the RidA family, but its role in D-Glu catabolism remains to be determined. "
09/01/2014 - "This work expands our understanding of the role played by RidA in preventing enamine stress resulting from multiple normal metabolic processes. "
07/01/2014 - "enterica, the Ser-derived enamine/imine inactivates a branched-chain aminotransferase; RidA prevents this damage. "
07/01/2014 - "enterica RidA and its homologs from other organisms hydrolyze the enamine/imine intermediates that Thr dehydratase forms from Ser or Thr. "
|2.||Dehydration (Water Stress)
10/26/2007 - "The direct addition of amine as well as the dehydration of the resulting carbinolamine intermediate is predicted to possess fairly high activation barrier implying that a unimolecular process is unlikely to be responsible for enamine formation. "
12/01/2014 - "The structural basis for the different chemical fates and lifetimes of the central enamine intermediates in all five enzymes will be particularly discussed, in addition to the mechanisms of substrate cleavage, dehydration and ring-opening reactions of cyclic substrates. "
10/26/2007 - "The addition of secondary amine to the electrophile and simultaneous proton transfer results in a carbinolamine intermediate, which subsequently undergoes dehydration to form enamine. "
11/21/2008 - "Conjugate addition of guanidine to a bis enone followed by an intramolecular Michael reaction of the enolate to the other enone, aldol reaction, dehydration, and enamine formation will lead to a tricyclic intermediate at the dehydroptilocaulin oxidation state. "
12/28/2004 - "This coenzyme forms a Schiff base with the keto sugar substrate and the resulting adduct undergoes a PMP-mediated beta-dehydration reaction to give a sugar enamine intermediate, which after tautomerization and hydrolysis to release ammonia yields GDP-4-keto-3,6-dideoxy-D-mannose as the product. "
|4.||Bites and Stings (Sting)
03/19/2009 - "In this reaction, the choice of a large-bite angle ligand Xantphos and proline as the organocatalyst was essential for generation of the crucial pi-allyl Pd intermediate from allylic alcohol, followed by nucleophilic attack of the enamine formed in situ from the corresponding enolizable carbonyl substrate and proline."
|2.||Proteins (Proteins, Gene)
|5.||Guanidine (Guanidine Nitrate)
|8.||Schiff Bases (Schiff Base)
|1.||Transplantation (Transplant Recipients)