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Asymmetric Epoxidation Of Dihydronaphthalene With A Synthesized Jacobsen's Catalyst
Part one of term paper
Asymmetric Epoxidation of Dihydronaphthalene with a Synthesized Jacobsen's
Chem 250 GG
Abstract. 1,2 diaminocyclohexane was reacted with L-(+)-tartaric acid to yield
(R,R)-1,2-diaminocyclohexane mono-(+)-tartrate salt. The tartrate salt was then
reacted with potassium carbonate and 3,5-di-tert-butylsalicylaldehyde to yield
(R,R)-N,N'-Bis(3, ...
Part two of term paper ... as well as
naphthalene.
Introduction
In 1990, professor E.N. Jacobsen reported that chiral manganese
complexes had the ability to catalyze the asymmetric epoxidation of
unfunctionalized alkenes, providing enantiomeric excesses that regularly
reaching 90% and sometimes exceeding 98% . The chiral manganese complex
Jacobsen utilized was [(R,R)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-
cyclohexanediaminato-(2-)]-manganese (III) chloride (Jacobsen's Catalyst).
(R,R) Jacobsen's Cat ...
Word count: 2135 | Approximate pages: 8
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