Optimizing the Dialkylation and Hydrolysis of Imines

Presentation Type

Poster

Keywords

Organic Chemistry

Department

Chemistry

Major

Chemistry

Abstract

This research is the further development of the first step in this sequence, the dialkylation and hydrolysis of an imine, to make a variety of disubstituted cyclopentanones, cyclohexanones and cycloheptanones as mixtures of the cis and trans diastereomers to be used in bisannulation of a ring to make tricyclo compounds.

Faculty Mentor

Dr. White

Funding Source or Research Program

Summer Undergraduate Research Program

Location

Waves Cafeteria

Start Date

29-3-2019 2:00 PM

End Date

29-3-2019 3:00 PM

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Mar 29th, 2:00 PM Mar 29th, 3:00 PM

Optimizing the Dialkylation and Hydrolysis of Imines

Waves Cafeteria

This research is the further development of the first step in this sequence, the dialkylation and hydrolysis of an imine, to make a variety of disubstituted cyclopentanones, cyclohexanones and cycloheptanones as mixtures of the cis and trans diastereomers to be used in bisannulation of a ring to make tricyclo compounds.