Stereoselective reaction of 2-carboxythioesters-1,3-dithiane with nitroalkenes: an organocatalytic strategy for the asymmetric addition of a glyoxylate anion equivalent.
about
Phosphazene-catalyzed desymmetrization of cyclohexadienones by dithiane addition.Photoredox radical conjugate addition of dithiane-2-carboxylate promoted by an iridium(iii) phenyl-tetrazole complex: a formal radical methylation of Michael acceptors.Direct catalytic enantioselective Mannich-type reaction of α,α-dithioacetonitriles with imines using chiral bis(imidazoline)-Pd complexes.The squaramide-catalyzed asymmetric Michael/cyclization tandem reaction for the synthesis of chiral trifluoromethylated hydroxyimino tetrahydrobenzofuranones.
P2860
Stereoselective reaction of 2-carboxythioesters-1,3-dithiane with nitroalkenes: an organocatalytic strategy for the asymmetric addition of a glyoxylate anion equivalent.
description
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name
Stereoselective reaction of 2- ...... a glyoxylate anion equivalent.
@en
Stereoselective reaction of 2- ...... a glyoxylate anion equivalent.
@nl
type
label
Stereoselective reaction of 2- ...... a glyoxylate anion equivalent.
@en
Stereoselective reaction of 2- ...... a glyoxylate anion equivalent.
@nl
prefLabel
Stereoselective reaction of 2- ...... a glyoxylate anion equivalent.
@en
Stereoselective reaction of 2- ...... a glyoxylate anion equivalent.
@nl
P2093
P2860
P50
P356
P1476
Stereoselective reaction of 2- ...... a glyoxylate anion equivalent.
@en
P2093
Andrea Genoni
Elisabetta Massolo
Giuseppe Celentano
P2860
P304
P356
10.1039/C5OB00492F
P577
2015-04-17T00:00:00Z