Journal ArticleOPEN ACCESS

Tandem Mannich/Diels-Alder reactions for the synthesis of indole compound libraries

RSC Advances (2016) 6(52) 46654-46657
DOI: 10.1039/c6ra08786h
12Citations
Citations of this article
18Readers
Mendeley users who have this article in their library.

Abstract

A tandem Mannich/Diels-Alder sequence for the synthesis of small-molecule libraries with an indolyl-octahydro-3a,6-epoxy-isoindole core structure is demonstrated in this study. Representative diversification examples based on this scaffold were performed, and a library is being produced within the European Lead Factory (ELF) Consortium.

Cite

CITATION STYLE

APA

Wu, P., Petersen, M. Å., Petersen, R., Flagstad, T., Guilleux, R., Ohsten, M., … Clausen, M. H. (2016). Tandem Mannich/Diels-Alder reactions for the synthesis of indole compound libraries. RSC Advances, 6(52), 46654–46657. https://doi.org/10.1039/c6ra08786h

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free