Publication | Closed Access
Synthesis of natural-product-like scaffolds in unprecedented efficiency via a 12-fold branching pathway
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Citations
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2011
Year
Tissue EngineeringCombinatorial ChemistryEngineeringMolecular BiologyBiofabricationOrganic ChemistryDiversity Oriented SynthesisTandem ReactionsKnot TheorySustainable SynthesisNatural-product-like ScaffoldsSeparate Tandem ReactionsDiversity-oriented SynthesisDiverse ScaffoldsNatural Product SynthesisBiomolecular EngineeringUnprecedented EfficiencyNatural Sciences12-Fold Branching PathwaySynthetic BiologySynthetic Chemistry
Tying the knot! The marriage of two-directional synthesis and tandem reactions allows access to twelve skeletally diverse scaffolds in just fifteen reactions. Two-directional synthesis yields a symmetrical linear “rope-like” keto-dienoate which is then subjected to twelve separate tandem reactions to “tie the rope in knots” thus creating twelve diverse natural product-like scaffolds containing useful functionality for further elaboration.
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