Formation and Reactivity of Triplet Vinylnitrenes as a Function of Ring Size-Reference-Cited by-同舟云学术

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Formation and Reactivity of Triplet Vinylnitrenes as a Function of Ring Size

Published:2019-07-02 Issue:14 Volume:84 Page:9215-9225
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Gatlin DeVonna M.¹,Karney William L.²^ORCID,Abe Manabu³^ORCID,Ault Bruce S.¹^ORCID,Gudmundsdottir Anna D.¹^ORCID

Affiliation:

1. Department of Chemistry, University of Cincinnati, Cincinnati, Ohio 45221, United States

2. Department of Chemistry, University of San Francisco, 2130 Fulton Street, San Francisco, California 94117, United States

3. Department of Chemistry, Graduate School of Science, Hiroshima University, Hiroshima 739-8526, Japan

Funder

Division of Chemistry

University of Cincinnati

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b01191

Reference53 articles.

1. Organic Azides: An Exploding Diversity of a Unique Class of Compounds

2. α-Substituted vinyl azides: an emerging functionalized alkene

3. 1,3-Dipolar Cycloaddition Reactivities of Perfluorinated Aryl Azides with Enamines and Strained Dipolarophiles

4. Iterative In Situ Click Chemistry Creates Antibody-like Protein-Capture Agents

5. Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides

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