Combinatorial chemistry and high-throughput screening for the discovery of 
organocatalysts

Hechavarrı́a Fonseca, Marı́a; List, Benjamin

doi:10.1016/j.cbpa.2004.04.013

Item

ITEM ACTIONSEXPORT

Add to Basket

Local TagsRelease HistoryDetailsSummary

Released

Journal Article

Combinatorial chemistry and high-throughput screening for the discovery of organocatalysts

MPS-Authors

/persons/resource/persons58610

Hechavarrı́a Fonseca, Marı́a
Research Department List, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

/persons/resource/persons58764

List, Benjamin
Research Department List, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

External Resource

No external resources are shared

Fulltext (restricted access)

There are currently no full texts shared for your IP range.

Fulltext (public)

There are no public fulltexts stored in PuRe

Supplementary Material (public)

There is no public supplementary material available

Citation

Hechavarrı́a Fonseca, M., & List, B. (2004). Combinatorial chemistry and high-throughput screening for the discovery of organocatalysts. Current Opinion in Chemical Biology, 8(3), 319-326. doi:10.1016/j.cbpa.2004.04.013.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0014-A4B6-D

Abstract

In recent years, interest in organocatalysis, the catalysis with small organic molecules, has been revitalized. Independently, high-throughput-screening and combinatorial chemistry became practical methodologies in the discovery of novel catalytic entities. The logical extension of these methodologies to organocatalysis has led to several interesting results, which are highlighted in this review.