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Synthesis of non-racemic pyrazolines and pyrazolidines by [3+2] cycloadditions of azomethine imines
ID Požgan, Franc (Author), ID Al Mamari, Hamad (Author), ID Grošelj, Uroš (Author), ID Svete, Jurij (Author), ID Štefane, Bogdan (Author)

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Abstract
Asymmetric [3+2] cycloadditions of azomethine imines comprise a useful synthetic tool for the construction of pyrazole derivatives with a variable degree of saturation and up to three stereogenic centers. As analogues of pyrrolidines and imidazolidines that are abundant among natural products, pyrazoline and pyrazolidine derivatives represent attractive synthetic targets due to their extensive applications in the chemical and medicinal industries. Following the increased understanding of the mechanistic aspect of metal-catalyzed and organocatalyzed [3+2] cycloadditions of 1,3-dipoles gained over recent years, significant strides have been taken to design and develop new protocols that proceed efficiently under mild synthetic conditions and duly benefit from superior functional group tolerance and selectivity. In this review, we represent the current state of the art in this field and detailed methods for the synthesis of non-racemic pyrazolines and pyrazolidines via [3+2] metal and organocatalyzed transformations reported since the seminal work of Kobayashi et al. and Fu et al. in 2002 and 2003 up to the end of year 2017.

Language:English
Keywords:pyrazolines, pyrazolidines, metal-catalyzed cycloadditions, organocatalyzed cycloadditions, azomethine imines, [3+2] cycloadditions
Work type:Article
Typology:1.02 - Review Article
Organization:FKKT - Faculty of Chemistry and Chemical Technology
Publication status:Published
Publication version:Version of Record
Year:2018
Number of pages:31 str.
Numbering:Vol. 23, iss. 1, art. 3
PID:20.500.12556/RUL-131880 This link opens in a new window
UDC:547.77
ISSN on article:1420-3049
DOI:10.3390/molecules23010003 This link opens in a new window
COBISS.SI-ID:1537674179 This link opens in a new window
Publication date in RUL:05.10.2021
Views:506
Downloads:140
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Record is a part of a journal

Title:Molecules
Shortened title:Molecules
Publisher:MDPI
ISSN:1420-3049
COBISS.SI-ID:18462981 This link opens in a new window

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:01.01.2018

Secondary language

Language:Slovenian
Keywords:pirazolini, pirazolidini, kovinsko katalizirane cikloadicije, organokatalizirane cikloadicije, azometin imini, [3+2] cikloadicije

Projects

Funder:ARRS - Slovenian Research Agency
Project number:P1-0179
Name:Sinteze in transformacije organskih spojin. Novi reagenti v stereoselektivni in regioselektivni sintezi aminokislin kot intermediatov v organski sintezi

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