Synthesis of 2-(Di/tri/tetraazolyl)-2H-azirine-2-carboxylates by Halogen Substitution: Evidence for an SN2′-SN2′ Cascade Mechanism-Reference-Cited by-同舟云学术

Synthesis of 2-(Di/tri/tetraazolyl)-2H-azirine-2-carboxylates by Halogen Substitution: Evidence for an SN2′-SN2′ Cascade Mechanism

Published:2018-10-10 Issue:21 Volume:83 Page:13473-13480
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Agafonova Anastasiya V.¹^ORCID,Rostovskii Nikolai V.¹^ORCID,Smetanin Ilia A.¹^ORCID,Starova Galina L.¹^ORCID,Khlebnikov Alexander F.¹^ORCID,Novikov Mikhail S.¹^ORCID

Affiliation:

1. St. Petersburg State University, Institute of Chemistry, 7/9 Universitetskaya nab., St. Petersburg 199034, Russia

Funder

Russian Science Foundation

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.8b02295

Reference32 articles.

1. Ring Expansions of Azirines and Azetines

2. The Chemistry of Transition Metals with Three-Membered Ring Heterocycles

3. Exploiting 2-Halo-2H-Azirine Chemistry

4. Rh(II)-carbenoid mediated 2H-azirine ring-expansion as a convenient route to non-fused photo- and thermochromic 2H-1,4-oxazines

5. Fe(II)-Catalyzed Amination of Aromatic C−H Bonds via Ring Opening of 2H-Azirines: Synthesis of 2,3-Disubstituted Indoles

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