A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones-Reference-Cited by-同舟云学术

A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones

Published:2018 Issue:4 Volume:5 Page:595-605
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Filatov A. S.¹²³,Knyazev N. A.⁴²³⁵²,Ryazantsev M. N.¹²³⁴²,Suslonov V. V.¹²³^ORCID,Larina A. G.¹²³,Molchanov A. P.¹²³,Kostikov R. R.¹²³,Boitsov V. M.⁴²³⁶⁷^ORCID,Stepakov A. V.¹²³⁸⁹^ORCID

Affiliation:

1. Saint-Petersburg State University

2. St. Petersburg

3. Russian Federation

4. Saint-Petersburg Academic University – Nanotechnology Research and Education Centre RAS

5. Institute of Cytology of the Russian Academy of Science

6. Pavlov First Saint Petersburg State Medical University

7. St. Petersburg 197022

8. Voeikov Main Geophysical Observatory

9. St. Petersburg 194021

Abstract

A simple and efficient synthesis of compounds with spiro-fused 11H-indeno[1,2-b]quinoxaline and azabicyclo[3.1.0]hexane or cyclopropa[a]pyrrolizine moieties was developed.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/QO/C7QO00888K

Reference75 articles.

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2. J. J. Tufariello , 1,3-Dipolar Cycloaddition Chemistry , ed. A. Padwa , Wiley , New York , 1984 , vol. 2 , p. 83

3. R. C. F. Jones and J. N.Martin , Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products , ed. A. Padwa and W. Pearson , Wiley , New York , 2002 , p. 1

4. Asymmetric 1,3-Dipolar Cycloaddition Reactions

5. J. W. Lown , 1,3-Dipolar Cycloaddition Chemistry , ed. A. Padwa , Wiley , New York , 1984 , vol. 1 , p. 2

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