Loading…
This event has ended. View the official site or create your own event → Check it out
This event has ended. Create your own

For Campus Prearrival Information <click here>
For a PDF of the 2015 Program Materials <click here>
For ALL Abstracts [1-220] in sequential order <click here>
For ALL Authors of the Lecture and Poster Presentations <click here>


View analytic
Monday, August 24 • 3:40pm - 4:00pm
[0140] The simple and versatile synthesis of tetrasubstituted pyrroles and subsequent functionalization

Sign up or log in to save this to your schedule and see who's attending!

Limited Capacity seats available

The cycloaddition–retroelectrocyclization reaction is a useful reaction for the conversion of electron-rich alkynes and electron-poor alkenes into buta-1,3-dienes.1 We have recently shown that this reaction is more widely applicable to ester-substituted alkenes to afford compounds of type 1.2 In this presentation we will describe how compounds of type 1 can be efficiently and rapidly converted into highly substituted pyrroles 2. Further one-step functionalization allows isolation of substituted pyrroles of type 3 and, 4 and 2H-pyrrol-2-ones 5, the latter of which exhibit strong chromophoric behaviour and a bathochromic shift upon protonation

ST Lecturers


Monday August 24, 2015 3:40pm - 4:00pm
UCEN Lobero