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Journal ArticleDOI

Recent advances in isocyanide-based multicomponent chemistry

Alexander Dömling
- 01 Jun 2002 - 
- Vol. 6, Iss: 3, pp 306-313
TLDR
Multicomponent reactions (MCRs) provide a powerful tool towards the one-pot synthesis of diverse and complex compounds on the one hand and small and 'drug-like' heterocycles on the other hand.
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This article is published in Current Opinion in Chemical Biology.The article was published on 2002-06-01. It has received 444 citations till now.

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Citations
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Journal ArticleDOI

Chemistry and Biology Of Multicomponent Reactions

TL;DR: This paper presents a new approach to drug design called “combinatorial biosynthesis and drug discovery through nanofiltration”, which combines the efforts of a single investigator with those of a number of other scientists.
Journal ArticleDOI

Asymmetric multicomponent reactions (amcrs): the new frontier

TL;DR: Asymmetric multicomponent reactions involve the preparation of chiral compounds by the reaction of three or more reagents added simultaneously and has some advantages over classic divergent reaction strategies, such as lower costs, time, and energy, as well as environmentally friendlier aspects.
Journal ArticleDOI

Organic Synthesis “On Water”

TL;DR: The currently burgeoning field of organic synthesis in aqueous media encompasses a large family of reactions, and water is still not commonly used as a sole solvent for organic synthesis, at least in part because most organic compounds do not dissolve in water to a significant extent.
Journal ArticleDOI

Recent Developments in the Isonitrile‐Based Multicomponent Synthesis of Heterocycles

TL;DR: A review of isocyanide-based multicomponent reactions for heterocycle synthesis can be found in this paper, where the authors advocate a "substrate-design approach" in searching for novel MCRs.
References
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Journal ArticleDOI

Multicomponent Reactions with Isocyanides.

TL;DR: MCRs and especially MCRs with isocyanides offer many opportunities to attain new reactions and basic structures, however, this requires that the chemist learns the "language" of M CRs, something that this review wishes to stimulate.
Journal ArticleDOI

Structural basis for the interaction of antibiotics with the peptidyl transferase centre in eubacteria

TL;DR: The details of antibiotic interactions with the components of their binding sites are reported and the importance of putative Mg+2 ions for the binding of some drugs is shown to facilitate rational drug design.
Book

The Logic of Chemical Synthesis

E. J. Corey, +1 more
TL;DR: A general approach to the analysis of complex synthetic problems: the basis for retrosynthetic analysis transform-based strategies structure-based and topological strategies stereochemical strategies functional group based and other strategies concurrent use of several strategies.
Journal ArticleDOI

Pairwise use of complexity-generating reactions in diversity-oriented organic synthesis.

TL;DR: Two pairs of complexity-generating reactions with an essential product-substrate relationship along a synthetic pathway are demonstrated, illustrating a key element in a planning algorithm for diversity-oriented synthesis.
Journal ArticleDOI

Isonitrile, II. Reaktion von Isonitrilen mit Carbonylverbindungen, Aminen und Stickstoffwasserstoffsäure

TL;DR: In this article, der Chemismus der Reaktion und ihr Anwendungsbereich werden diskutiert, i.e., der chemismus of reaction and i. e. g.
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