Nikolay S. Kondratyev
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View article: Asymmetric organocatalytic synthesis of chiral homoallylic amines
Asymmetric organocatalytic synthesis of chiral homoallylic amines Open
In recent decades, the chiral allylation of imines emerged as a key methodology in the synthesis of alkaloids and natural products with 4-, 5- and 6-membered cyclic amine motifs. Initially reliant on stoichiometric reagents, synthetic chem…
View article: Organocatalytic asymmetric alkenylation of carbonyl compounds
Organocatalytic asymmetric alkenylation of carbonyl compounds Open
Asymmetric alkenylation of carbonyl compounds using organocatalysed reaction with respective organoelement reagents has developed into a useful and practically important method for the synthesis of enantiomerically enriched homoallylic ami…
View article: Kinetic resolution of chiral racemic secondary allylboronates and their application in the synthesis of homoallylic amines [Abstract]
Kinetic resolution of chiral racemic secondary allylboronates and their application in the synthesis of homoallylic amines [Abstract] Open
Kinetic resolution of chiral racemic secondary allylboronates and their application in the synthesis of homoallylic amines [Abstract]
View article: Kinetic Resolution of Secondary Allyl Boronates and Their Application in the Synthesis of Homoallylic Amines
Kinetic Resolution of Secondary Allyl Boronates and Their Application in the Synthesis of Homoallylic Amines Open
Highly enantioenriched, chromatographically‐stable secondary allyl boronates featuring a 1,1,2,2‐tetraethyl‐1,2‐ethanediol fragment (Epin) were obtained by kinetic resolution of their racemic mixtures. The Epin group at boron considerably …
View article: CCDC 1848858: Experimental Crystal Structure Determination
CCDC 1848858: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …