Events The 4th International Electronic Conference on Synthetic Organic Chemistry

Event submissions

Published

This submission belongs to the session a. General Organic Synthesis of the event The 4th International Electronic Conference on Synthetic Organic Chemistry

Published date

11 Sep, 2000

Citation

Alexander D. Vasiliev, Ludmila A. Kruglyakova, Rudolf S. Stepanov, Oksana A. Golubtsova, Konstantin V. Pekhotin, Mark V. Rogozin, Synthesis of 2-nitromethyl-5-nitro-1,2,3,4-tetrazole, in Proceedings of The 4th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2000, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-4-01877

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Synthesis of 2-nitromethyl-5-nitro-1,2,3,4-tetrazole

Mark V. Rogozin ¹

Konstantin V. Pekhotin ¹

Oksana A. Golubtsova ¹

Rudolf S. Stepanov ¹

Ludmila A. Kruglyakova ¹

Alexander D. Vasiliev ²

1. Siberian State Technological University, pr. Mira 82, Krasnoyarsk, 660049, Russian Federation

2. Krasnoyarsk State University, Institut of Physics, Krasnoyarsk, 660036, Russian Federation.

Abstract

One of most interesting objects for studying the ability of polyfunctional nucleophiles is the nitromethyl derivatives series of 1,2,3,4-tetrazole, which also have wide practical application. Some derivatives in that series can be used for the synthesis of medicinal preparations, however in the literature there is no information on the synthesis of mononitrometyltetrazoles with nitromethyl’s group in position 2. The aim of this work was to synthesize 2-nitromethyl-5-nitro-1,2,3,4-tetrazole (NMNT) and to investigate its structure.

Keywords

n/a

Enantioselective hydride abstraction in organic substrates: future applications for chiral carbenium ions

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