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Beilstein J. Org. Chem. 2014, 10, 929–935, doi:10.3762/bjoc.10.91
Graphical Abstract
Figure 1: Oxindole based Michael acceptors.
Figure 2: Primary-tertiary diamine organocatalysts.
Scheme 1: Diamine catalyzed Michael addition of acetone to isatylidenemalononitrile.
Scheme 2: Substrate scope of the addition of 2 with 3 catalyzed by 1a D-CSA.
Scheme 3: One-pot, three-component Knoevenagel condensation–Michael addition.
Scheme 4: Cascade reduction–cyclization for the synthesis of spirooxindole.
Beilstein J. Org. Chem. 2012, 8, 2132–2141, doi:10.3762/bjoc.8.240
Scheme 1: Proline-catalysed aldol reaction in a ball-mill.
Scheme 2: Proline-catalysed aldol reaction between solid substrates (1b and 2a).
Scheme 3: (S)-Binam-L-prolinamide catalysed asymmetric aldol reaction by using a ball-mill. aConversion.
Scheme 4: Asymmetric aldol reaction assisted by ball-milling catalysed by dipeptides (A) with III and (B) wit...
Scheme 5: Thiodipeptide-catalysed asymmetric aldol reaction of (A) ketones with aldehydes and (B) acetone wit...
Scheme 6: Enantioselective Michael reaction of aldehydes with nitroalkenes catalysed by pyrrolidine-derived o...
Scheme 7: Chiral squaramide catalysed asymmetric Michael reaction assisted by ball-milling.
Scheme 8: Asymmetric organocatalytic Michael reaction assisted by pestle and mortar grinding.
Scheme 9: C-2 symmetric thiourea catalysed enantioselective MBH reaction.
Scheme 10: Quinine-catalysed ring opening of meso-anhydride by ball-milling.
Scheme 11: Ball-milling-assisted (A) synthesis of glycine schiff bases and (B) their organocatalytic asymmetri...
Scheme 12: Enantioselective amination of β-ketoester by using pestle and mortar.