Simple exploration of 19132-06-0

Therefore, this conceptually novel strategy might open impressive avenues to establish green and sustainable chemistry platforms.In my other articles, you can also check out more blogs about19132-06-0.name: (2S,3S)-Butane-2,3-diol

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, name: (2S,3S)-Butane-2,3-diol, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. name: (2S,3S)-Butane-2,3-diol, Name is (2S,3S)-Butane-2,3-diol, molecular formula is C4H10O2. In a Article, authors is Monsalve, Leandro N.£¬once mentioned of name: (2S,3S)-Butane-2,3-diol

Rhodotorula minuta-mediated bioreduction of 1,2-diketones

The reduction of cyclic and acyclic 1,2-diketones was investigated by employing whole cells of the yeast Rhodotorula minuta as biocatalyst. The reactions showed a variable degree of regio- and enantioselectivity depending on the nature of the substrate. In the case of cyclic diketones, the reduction afforded a mixture of diastereomeric diols only. The reduction of acyclic diketones allowed production of both the hydroxy ketone and the diol, in a two-step reaction. The first step was highly regio- and stereoselective, affording the hydroxy ketone of (S)-configuration with high enantiomeric excess. After longer reaction times the corresponding (S,S)-diols were obtained in high yield and diastereomeric excess.

Therefore, this conceptually novel strategy might open impressive avenues to establish green and sustainable chemistry platforms.In my other articles, you can also check out more blogs about19132-06-0.name: (2S,3S)-Butane-2,3-diol

Reference£º
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate