0000000001316162
AUTHOR
David Sanz
Enantioselective zinc-mediated conjugate alkynylation of saccharin-derived 1-aza-butadienes
The enantioselective 1,4-alkynylation of conjugated imines derived from saccharin with aryl- and alkyl-substituted terminal alkynes has been achieved. The reaction mediated by diethylzinc in the presence of a catalytic amount of a bis(hydroxy)malonamide chiral ligand provides the corresponding imines bearing a propargylic stereocenter with moderate yields and fair to excellent enantioselectivities.
High-Quality Whole-Genome Sequence of an Estradiol-Degrading Strain, Novosphingobium tardaugens NBRC 16725
In this work we report the complete sequence and assembly of the estradiol-degrading bacterium Novosphingobium tardaugens NBRC 16725 genome into a single contig using the Pacific Biosciences RS II system.
CCDC 1992564: Experimental Crystal Structure Determination
Related Article: Gonzalo Blay, Alvaro Castilla, David Sanz, Amparo Sanz-Marco, Carlos Vila, M. Carmen Muñoz, José R. Pedro|2020|Chem.Commun.|56|9461|doi:10.1039/D0CC04221H