5.37 | Spring 2009 | Undergraduate

Introduction to Organic Synthesis Laboratory

Cyclopentadiene reacting with methacrolein to form different norbornene enantiomers

Description:

Asymmetric Diels-Alder reaction of cyclopentadiene and methacrolein. The chiral acyloxyborane catalyst (CAB) helps control the stereochemical outcome of this cycloaddition reaction. (Image by MIT OpenCourseWare.)

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Cyclopentadiene reacting with methacrolein to form different norbornene enantiomers
Alt text:
Cyclopentadiene reacting with methacrolein to form different norbornene enantiomers.
Caption:
Asymmetric Diels-Alder reaction of cyclopentadiene and methacrolein. The chiral acyloxyborane catalyst (CAB) helps control the stereochemical outcome of this cycloaddition reaction. (Image by MIT OpenCourseWare.)
Cyclopentadiene reacting with methacrolein to form different norbornene enantiomers.

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Spring 2009
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