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Beilstein J. Org. Chem. 2016, 12, 301–308, doi:10.3762/bjoc.12.32
Graphical Abstract
Scheme 1: Cascade 1,2-difunctionalization and cyclization to construct heterocycles.
Scheme 2: Cyclization of cyclohexane (2a) with substituted N-(2-methylallyl)benzamide (reaction conditions: 4...
Scheme 3: Cyclization of cycloalkanes with N-methyl-N-(2-methylallyl)benzamide (reaction conditions: 4a (0.2 ...
Scheme 4: Cyclization reaction of 6 with cyclohexane 2a (reaction conditions: 6 (0.2 mmol), cyclohexane 2a (2...
Scheme 5: Control experiments for the mechanism studies. a) Reaction with N-unprotected substrate 8a; b) reac...
Scheme 6: Proposed mechanism.
Beilstein J. Org. Chem. 2014, 10, 1802–1807, doi:10.3762/bjoc.10.189
Scheme 1: An anomalous outcome with benzylamine as organic base.
Scheme 2: Transformation of vicinal haloamines by the use of organic amines.
Figure 1: ORTEP diagram of compound 5o.
Scheme 3: Ring-opening of aziridine 6.
Scheme 4: Proposed mechanism.
Beilstein J. Org. Chem. 2014, 10, 969–974, doi:10.3762/bjoc.10.95
Figure 1: Decarboxylative aldol reactions of β-keto acids with aldehydes.
Figure 2: Nucleophilic reaction of α-keto esters to generate tertiary alcohols.
Figure 3: Decarboxylative aldol reactions of β-keto acids with α-keto esters.
Scheme 1: Asymmetric decarboxylative aldol reaction of various β-keto acids with α-keto esters under optimise...
Scheme 2: Proposed mechanism of decarboxylative aldol reaction.