Domino reactions of diazodicarbonyl compounds with α,β-unsaturated δ-amino esters: a convenient way towards 2-oxopiperidines, dihydropyridinones and isoquinolinediones-Reference-Cited by-同舟云学术

Domino reactions of diazodicarbonyl compounds with α,β-unsaturated δ-amino esters: a convenient way towards 2-oxopiperidines, dihydropyridinones and isoquinolinediones

Published:2015 Issue:34 Volume:13 Page:9107-9117
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Medvedev J. J.¹²³,Meleshina M. V.¹²³,Panikorovskii T. L.¹²³,Schneider C.⁴⁵⁶⁷,Nikolaev V. A.¹²³

Affiliation:

1. Saint-Petersburg State University

2. St.-Petersburg 198504

3. Russia

4. Universität Leipzig

5. Institut für Organische Chemie

6. D-04103 Leipzig

7. Germany

Abstract

Thermal decomposition of a series of diazodicarbonyl compounds in the presence of α,β-unsaturated δ-amino esters and sodium hydride gives rise to a variety of nitrogenous heterocycles.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/OB/C5OB01197C

Reference53 articles.

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2. L. F. Tietze , Domino Reactions: Concepts for Efficient Organic Synthesis, Wiley-VCH, Weinheim, 2014, p. 648

3. Recent advances in the chemistry of Rh carbenoids: multicomponent reactions of diazocarbonyl compounds

4. Domino reactions of rhodium(ii) carbenoids for alkaloid synthesis

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