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Beilstein J. Org. Chem. 2015, 11, 622–627, doi:10.3762/bjoc.11.70
Graphical Abstract
Scheme 1: Synthesis of enamines from ketones with percentage yields.
Scheme 2: Branched-selective intramolecular hydroaminovinylation (60% isolated yield of 1j).
Scheme 3: Conversion of 1e to 2e using ligands 4–9.
Beilstein J. Org. Chem. 2007, 3, No. 24, doi:10.1186/1860-5397-3-24
Scheme 1: Microwave promoted ene reaction of ethyl trifluoropyruvate with α-methyl styrene.
Scheme 2: Thiourea catalysed ene reaction.
Scheme 3: Asymmetric carbonyl ene reaction mediated by chiral thiourea.
Scheme 4: Reaction between ethyl trifluoropyruvate and various alkenes.
Beilstein J. Org. Chem. 2007, 3, No. 18, doi:10.1186/1860-5397-3-18
Scheme 1: Catalysts used in this study and microwave accelerated cross-coupling of functionalised boronic aci...
Scheme 2: Microwave accelerated cross-coupling of a range of boronic acids with 4-chloroacetophenone.
Scheme 3: Competition experiment demonstrating the inhibitory effect of 2,3,6-trifluorophenyl boronic acid on...
Scheme 4: Stoichiometric reactions between fluorinated boronic acids and [Pd(dppf)Cl2].