cycloalkenyllithiumsreductive lithiation of tetrahydrofuranslithium–halogen exchangereductive lithiation of allylic acetalsring opening of azetidinesorganolithiumsThis article has no abstract.doi:10.1002/9780471264194.fos06410Tse-Lok HoMary FieserLouis FieserJanice SmithJohn Wiley & Sons, Inc....
Several procedures were evaluated for the preparation of lithium 4,4′-di-tert-butylbiphenylide (LiDBB, Freeman's reagent) from lithium metal and 4,4′-di-tert-butylbiphenyl (DBB) in THF. Solutions with nominal concentration of 0.4 and 1.0 M were formed. The stability of LiDBB solutions was...
Several procedures were evaluated for the preparation of lithium 4,4′-di-tert-butylbiphenylide (LiDBB, Freeman's reagent) from lithium metal and 4,4′-di-tert-butylbiphenyl (DBB) in THF. Solutions with nominal concentration of 0.4 and 1.0 M were formed. The stability of LiDBB solutions was...
cycloalkenyllithiumsreductive lithiation of tetrahydrofuranslithium–halogen exchangereductive lithiation of allylic acetalsring opening of azetidinesorganolithiumsThis article has no abstract.doi:10.1002/9780471264194.fos06410.pub4Tse-Lok HoMary FieserLouis FieserJanice SmithJohn Wiley & Sons, Inc....
ChemInform Abstract: Synthesis of Organolithium Compounds Using Lithium 4,4′-Di- tertbutylbiphenylidecoordination chemistry, revieworgano-lithium compoundsChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ...
aryllithiumarylzincpalladiumcross-couplingWe report an efficient method for the preparation of aryllithium and zinc reagents from inexpensive and readily available aryl chlorides by using lithium 4,4′-di-tert-butylbiphenylide (LiDBB) as a lithiation reagent. The resulting organometallic reagents underwent...