Synthesis of Azanucleosides through Regioselective Ring-Opening of Epoxides Catalyzed by Sulphated Zirconia under Microwave and Solvent-Free Conditions-Reference-Cited by-同舟云学术

Synthesis of Azanucleosides through Regioselective Ring-Opening of Epoxides Catalyzed by Sulphated Zirconia under Microwave and Solvent-Free Conditions

Published:2012-03-15 Issue:3 Volume:17 Page:3359-3369
ISSN:1420-3049
Container-title:Molecules
language:en
Short-container-title:Molecules

Author:

Hernández-Reyes Celia Xochitl,Angeles-Beltrán Deyanira,Lomas-Romero Leticia,González-Zamora Eduardo,Gaviño Rubén,Cárdenas Jorge,Morales-Serna José Antonio,Negrón-Silva Guillermo E.

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

Link

http://www.mdpi.com/1420-3049/17/3/3359/pdf

Reference38 articles.

1. Active and recyclable sulphated zirconia catalysts for the acylation of aromatic compounds

2. n-Pentane Isomerization Over Pt- and Ni–Pt-Promoted Sulfated Zirconia Catalysts Supported on Alumina

3. Organic Syntheses and Transformations Catalyzed by Sulfated Zirconia

4. Organic syntheses catalyzed by superacidic metal oxides: sulfated zirconia and related compounds

5. An efficient synthesis of 6,6-dimethyl-2-(4-nitrophenyl)-1-(R-penyl)-4,5,6,7-tetrahydro-1H-4-indolones using a solid sulphated zirconia as catalyst;Negrón;Heterocycles,2004

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