Tandem Michael addition/elimination – novel reactivity of pyridinium ylides in reaction with electron-deficient alkenes-Reference-Cited by-同舟云学术

Tandem Michael addition/elimination – novel reactivity of pyridinium ylides in reaction with electron-deficient alkenes

Published:2022 Issue:18 Volume:9 Page:4998-5004
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Izmest'ev Alexei N.¹^ORCID,Motornov Vladimir A.²^ORCID,Vinogradov Dmitry B.¹^ORCID,Ioffe Sema L.¹,Kravchenko Angelina N.¹,Gazieva Galina A.¹^ORCID

Affiliation:

1. N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky Prosp., Moscow 119991, Russian Federation

2. Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo nám. 2, 160 00 Prague 6, Czech Republic

Abstract

Novel reactivity of pyridinium ylides in reaction with 4-oxothiazolidin-5-ylidenes as electron-deficient alkenes involving a tandem Michael addition/elimination process was developed to give double bond functionalization products in mild conditions.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/QO/D2QO00911K

Reference36 articles.

1. Intramolecular Dipolar Cycloaddition Reactions of Azomethine Ylides

2. Pyridinium Ylids in Heterocyclic Synthesis

3. Cyclative MCRs of Azines and Azinium Salts

4. Eco-friendly and sustainable synthetic approaches to biologically significant fused N-heterocycles

5. New applications of pyridinium ylides toward heterocyclic synthesis

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