Zinc(ii)-mediated generation of 5-amino substituted 2,3-dihydro-1,2,4-oxadiazoles and their further ZnII-catalyzed and O2-involving transformations-Reference-Cited by-同舟云学术

Zinc(ii)-mediated generation of 5-amino substituted 2,3-dihydro-1,2,4-oxadiazoles and their further ZnII-catalyzed and O2-involving transformations

Published:2015 Issue:12 Volume:39 Page:9330-9344
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Smirnov Andrey S.¹²³,Yandanova Ekaterina S.¹²³,Bokach Nadezhda A.¹²³,Starova Galina L.¹²³,Gurzhiy Vladislav V.¹²³,Avdontceva Margarita S.¹²³,Zolotarev Andrey A.¹²³,Kukushkin Vadim Yu.¹²³⁴⁵

Affiliation:

1. Saint Petersburg State University

2. 199034 Saint Petersburg

3. Russia

4. Institute of Macromolecular Compounds of Russian Academy of Sciences

5. 199004 Saint Petersburg

Abstract

Zn^II-activated cyanamides NCNR₂ react with the acyclic N-alkyl ketonitrones Ph₂CN⁺(O⁻)R′ achieving uncomplexed 2,3-dihydro-1,2,4-oxadiazoles.

Funder

Saint Petersburg State University

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2015/NJ/C5NJ02061A

Reference72 articles.

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5. P. H. H. Hermkens , N-Hydroxy-β-carbolines syntheses, applications, and biological activities, Dissertation, 1990, CAN 2012:1449457

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