‘Atypical Ugi’ tetrazoles-Reference-Cited by-同舟云学术

‘Atypical Ugi’ tetrazoles

Published:2020 Issue:12 Volume:56 Page:1799-1802
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Abdelraheem Eman M. M.¹²³⁴⁵,Goodwin Imogen¹²³⁴,Shaabani Shabnam¹²³⁴^ORCID,de Haan Michel P.¹²³⁴,Kurpiewska Katarzyna⁶⁷⁸⁹,Kalinowska-Tłuścik Justyna⁶⁷⁸⁹^ORCID,Dömling Alexander¹²³⁴^ORCID

Affiliation:

1. Department of Drug Design

2. University of Groningen

3. 9713 AV Groningen

4. The Netherlands

5. Chemistry Department

6. Faculty of Chemistry

7. Jagiellonian University

8. 30-060 Krakow

9. Poland

Abstract

We surprisingly found that combining the substrates of Ugi tetrazole reaction gives two different constitutional isomeric Ugi products A and B. A is the expected classical Ugi products whereas B is an isomeric product (‘atypical Ugi’).

Funder

Innovative Medicines Initiative

KWF Kankerbestrijding

Center for Scientific Review

Seventh Framework Programme

Horizon 2020 Framework Programme

European Regional Development Fund

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2020/CC/C9CC09194G

Reference32 articles.

1. 5-Substituted-1H-tetrazoles as carboxylic acid isosteres: medicinal chemistry and synthetic methods

2. 5-Aminotetrazole as a Building Block for Multicomponent Reactions (Review)

3. Tetrazoles via Multicomponent Reactions

4. Parallel Synthesis of Arrays of Amino-Acid-Derived Isocyanoamides Useful As Starting Materials in IMCR

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