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Cited by 209

The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.

1,3‐Dipolare Cycloaddition von Aziden und Alkinen: eine universelle Ligationsmethode in den Polymer‐ und Materialwissenschaften

Lutz, Jean‐François·2007·Angewandte Chemie

Abstract

Im Jahr 2001 stellten K. Barry Sharpless und Mitarbeiter in der Angewandten Chemie das Konzept der Klick‐Chemie vor, die eine Handvoll annähernd perfekt ablaufender chemischer Reaktionen umfasst. Unter diesen sorgfältig ausgewählten Reaktionen stellten sich 1,3‐dipolare Cycloadditionen nach Huisgen als die effizientesten und wandlungsfähigsten Reaktionen heraus und avancierten damit zum Paradebeispiel für die Klick‐Chemie. Aus diesem Grund erlangte dieser ursprünglich vernachlässigte Reaktionstyp plötzlich große Bedeutung in der organischen Synthese; speziell in den Materialwissenschaften wurden Cycloadditionen populär. Innerhalb der letzten zwei Jahre stieg die Zahl der Publikationen, die sich mit dem Thema Klick‐Chemie befassen, exponentiell an. Klick‐Chemie: Ein Wundermittel oder ein kurzlebiger Trend?

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Metadata

Authors
Lutz, J.
Venue
Angewandte Chemie
Publisher
Wiley
Published
2007-01-29
Volume
119
Issue
7
Pages
1036-1043
ISSN
  • 0044-8249 (ISSN-L)
  • 1521-3757
OpenAlex
W2165340338
Cited by
209
References
6
FWCI
16.09
Type
journal article
Language
de
Open access
closed

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CoChat. (2026). Citation check: 1,3‐Dipolare Cycloaddition von Aziden und Alkinen: eine universelle Ligationsmethode in den Polymer‐ und Materialwissenschaften. https://app.cochat.ai/papers/10.1002/ange.200604050
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Lutz, J. (2007). 1,3‐Dipolare Cycloaddition von Aziden und Alkinen: eine universelle Ligationsmethode in den Polymer‐ und Materialwissenschaften. Angewandte Chemie. https://doi.org/10.1002/ange.200604050

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