Publication | Closed Access
Stereoselective Solid‐Phase Synthesis of Cyclopentane and Cyclohexane Derivatives by Two‐Component Domino Reactions: Generation of Combinatorial Libraries
58
Citations
16
References
1996
Year
Bioorganic ChemistryEngineeringEne ReactionCombinatorial LibrariesOrganic ChemistryChemistryHeterocycle ChemistryStereoselective SynthesisBiochemistryDiversity-oriented SynthesisPolymer-bound Malonate 1Asymmetric CatalysisCyclohexane DerivativesEnantioselective SynthesisBiomolecular EngineeringHeterocyclicNatural SciencesStereoselective Solid‐phase SynthesisDiversomer Libraries
Diversomer libraries consisting of substituted cyclopentanes and cyclohexanes 3 were produced by Knoevenagel reaction of polymer-bound malonate 1 and aldehydes 2, subsequent ene reaction, and cleavage from the support. In this domino solid-phase procedure the simple and induced diastereoselectivities of the ene reaction are generally very satisfactory (>99:1). R = H, Me, nBu, Ph.
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