Zeitschrift für Naturforschung B · 1994 · 14 citations · 1 references
Trimethyltinlithium ReactsTrans-product 5EngineeringEthene DerivativesHeterocyclicStructure ElucidationOrganic ChemistryMain Group ChemistryChemistryHeterocycle ChemistryDerivative (Chemistry)Synthetic ChemistryBiomolecular EngineeringRadial Intermediate
Trimethyltinlithium reacts with z-1,2-bis(diisopropylamino-chloro-boryl)ethene derivatives 4a (R = Et) and 4b (R = H) to give the cis-1,2-bis(diisopropylamino-trimethyltin-boryl)- hexene-3 (2a) and, surprisingly, the trans-1,2-bis(diisopropylamino-trimethyltin-boryl)- ethene (5 b) respectively. The constitution of 2 a and 5 b is derived from spectroscopic data, and confirmed by X-ray structure analyses. The formation of the trans-product 5 b probably occurs via a radial intermediate.
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