Facile synthesis of 1,5-disubstituted tetrazoles by reacting a ruthenium acetylide complex with trimethylsilyl azide-Reference-Cited by-同舟云学术

Facile synthesis of 1,5-disubstituted tetrazoles by reacting a ruthenium acetylide complex with trimethylsilyl azide

Published:2019 Issue:31 Volume:48 Page:11732-11742
ISSN:1477-9226
Container-title:Dalton Transactions
language:en
Short-container-title:Dalton Trans.

Author:

Chang Chao-Wan¹²³⁴^ORCID,Cheng Ming-Chuan⁵⁶⁷⁴⁸^ORCID,Lee Gene-Hsiang⁹⁶⁷⁴,Peng Shie-Ming⁵⁶⁷⁴⁸

Affiliation:

1. Division of Preparatory Programs for Overseas Chinese Students

2. National Taiwan Normal University

3. New Taipei City 24449

4. Taiwan

5. Department of Chemistry

6. National Taiwan University

7. Taipei 10617

8. Institute of Chemistry

9. Instrumentation Center

Abstract

Synthesis of a series of 1,5-disubstituted tetrazoles by reacting a ruthenium acetylide complex with TMSN₃ and the alkylation of thus formed tetrazolates.

Funder

Ministry of Science and Technology, Taiwan

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/DT/C9DT02363A

Reference117 articles.

1. A review of syntheses of 1,5-disubstituted tetrazole derivatives

2. Synthesis and Functionalization of 5-Substituted Tetrazoles

3. Photochemical Transformations of Tetrazole Derivatives: Applications in Organic Synthesis

4. Fast Alkene Functionalization In Vivo by Photoclick Chemistry: HOMO Lifting of Nitrile Imine Dipoles

5. Selective Functionalization of a Genetically Encoded Alkene-Containing Protein via “Photoclick Chemistry” in Bacterial Cells

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