Publication | Closed Access
Enantiomerically Pure Cyclopropane Building Blocks: Synthesis and Transformations of 2‐Iodocyclopropylboronic Esters
35
Citations
30
References
2004
Year
Cross-coupling ReactionEngineeringHeterocyclicNatural SciencesDiversity-oriented SynthesisOrganic ChemistryEsters 6ChemistryUnique Building BlocksStereoselective SynthesisAsymmetric CatalysisEnantioselective SynthesisBiomolecular EngineeringVersatile Intermediates
Abstract Enantiomerically pure 2‐iodocyclopropylboronic esters 6 and 8 have been synthesized from the readily available allylic alcohol 2 via an oxidation‐radical decarboxylation sequence. These unique building blocks have been demonstrated to be versatile intermediates for a consecutive Suzuki‐coupling with aryl‐, heteroaryl‐, alkenyl‐, and cyclopropylboron derivatives (1 example each).
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