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Generating Diverse Skeletons of Small Molecules Combinatorially

Authors: Martin D, Burke; Eric M, Berger; Stuart L, Schreiber;

Generating Diverse Skeletons of Small Molecules Combinatorially

Abstract

Lack of efficient access to collections of synthetic compounds that have skeletal diversity is a key bottleneck in the small-molecule discovery process. We report a synthesis strategy that involves transforming substrates with different appendages that pre-encode skeletal information, named σ elements, into products that have different skeletons with the use of common reaction conditions. With this approach, split-pool synthesis can be used to pre-encode skeletal diversity combinatorially and thereby generate such small molecules very efficiently. A split-pool synthesis of more than 1000 compounds produced overlapping, combinatorial matrices of molecular skeletons and appended building blocks in both enantiomeric and diastereomeric forms.

Related Organizations
Keywords

Molecular Structure, Cyclization, Benzenesulfonates, Chemistry, Organic, Combinatorial Chemistry Techniques, Acetylation, Stereoisomerism, Furans, Hydroxylation, Oxidation-Reduction, Bromosuccinimide

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
338
Top 1%
Top 1%
Top 1%
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