Journal ArticleDOI
Asymmetric 1,3-Dipolar Cycloaddition Reactions
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This article is published in Chemical Reviews.The article was published on 1998-03-14. It has received 1661 citations till now. The article focuses on the topics: 1,3-Dipolar cycloaddition.read more
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A stepwise huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes.
Journal ArticleDOI
Click Chemistry: Diverse Chemical Function from a Few Good Reactions.
TL;DR: In this paper, a set of powerful, highly reliable, and selective reactions for the rapid synthesis of useful new compounds and combinatorial libraries through heteroatom links (C-X-C), an approach called click chemistry is defined, enabled, and constrained by a handful of nearly perfect "springloaded" reactions.
Journal ArticleDOI
Asymmetric multicomponent reactions (amcrs): the new frontier
Diego J. Ramón,Miguel Yus +1 more
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.
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‘Click’ Chemistry in Polymer and Materials Science
TL;DR: The metal catalyzed azide/alkyne "click" reaction (a variation of the Huisgen 1,3-dipolar cycloaddition reaction between terminal acetylenes and azides) represents an important contribution towards this endeavor.
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Click-Chemie: diverse chemische Funktionalität mit einer Handvoll guter Reaktionen
TL;DR: In this paper, the authors show how in der Natur am haufigsten vorkommenden Verbindungen, so fallt auf, dass the Bildung von Kohlenstoff-Heteroatom-Bindungen gegenuber der von KHO-Kohlenstoffs-KHO-Bindingsen deutlich bevorzugt is, and das Medium naturlicher Reaktionen zumeist Wasser ist.
References
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Book
1,3-Dipolar Cycloaddition Chemistry
TL;DR: The theory of 1-3-Dipolar Cycloadditions is discussed in this article. But it does not consider higher-order cycloaddings and higher order cycloreversions.
Journal ArticleDOI
1.3‐Dipolare Cycloadditionen Rückschau und Ausblick
TL;DR: In der 1.3-Dipol-Addition as mentioned in this paper, ein nur bescheidener Satz an Aufbaumethoden von allgemeiner Verwendungsbreite is gegenuber.
Journal ArticleDOI
Stereochemistry of Electrocyclic Reactions
Related Papers (5)
Construction of enantiopure pyrrolidine ring system via asymmetric [3+2]-cycloaddition of azomethine ylides.
Intramolecular dipolar cycloaddition reactions of azomethine ylides.
Iain Coldham,Richard Hufton +1 more