Copper-mediated oxidative [3 + 2]-annulation of nitroalkenes and pyridinium ylides: general access to functionalized indolizines and efficient synthesis of 1-fluoroindolizines-Reference-Cited by-同舟云学术

Copper-mediated oxidative [3 + 2]-annulation of nitroalkenes and pyridinium ylides: general access to functionalized indolizines and efficient synthesis of 1-fluoroindolizines

Published:2019 Issue:6 Volume:17 Page:1442-1454
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Motornov Vladimir A.¹²³⁴⁵^ORCID,Tabolin Andrey A.¹²³⁴^ORCID,Nelyubina Yulia V.⁶²³⁴^ORCID,Nenajdenko Valentine G.⁷⁸⁹⁴^ORCID,Ioffe Sema L.¹²³⁴^ORCID

Affiliation:

1. N. D. Zelinsky Institute of Organic Chemistry

2. Russian Academy of Sciences

3. Moscow

4. Russia

5. Higher Chemical College

6. A. N. Nesmeyanov Institute of Organoelement Compounds

7. Department of Chemistry

8. M. V. Lomonosov Moscow State University

9. Moscow 119991

Abstract

Novel 1-fluoroindolizines were obtained via copper(ii)-mediated oxidative [3 + 2]-annulation of in situ generated pyridinium ylides and fluoronitroalkenes.

Funder

Russian Foundation for Basic Research

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/OB/C8OB03126F

Reference106 articles.

1. Recent progress in synthesis and bioactivity studies of indolizines

2. Indolizine: a biologically active moiety

3. Synthesis and Biological Activity of Lamellarin Alkaloids: An Overview