Theoretically Predicted and Experimentally Detected Chirality of Dibenzocyclooctynes and Their Triazole Adducts with Azides-Reference-Cited by-同舟云学术

Theoretically Predicted and Experimentally Detected Chirality of Dibenzocyclooctynes and Their Triazole Adducts with Azides

Published:2023-10-20 Issue:21 Volume:88 Page:15097-15105
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Mazzoccanti Giulia¹^ORCID,Franzini Roberta¹^ORCID,Ciogli Alessia¹^ORCID,Pierini Marco¹,Buonsenso Fabio¹,Faggi Cristina²^ORCID,Francioso Antonio³,Manetto Simone¹,Villani Claudio¹^ORCID

Affiliation:

1. Department of Chemistry and Technology of Drugs, Excellence 2018–2022, Sapienza University of Rome, P.le Aldo Moro 5, Rome 00185, Italy

2. Department of Chemistry “Ugo Schiff”, University of Florence, Via della Lastruccia 3–13, Sesto Fiorentino I-50019, Italy

3. Department of Bioscience and Technology for Food, Agriculture and Environment, University of Teramo, Teramo 64100, Italy

Funder

Ministero dell’Istruzione, dell’Università e della Ricerca

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c01557

Reference25 articles.

1. Transition States of Strain-Promoted Metal-Free Click Chemistry: 1,3-Dipolar Cycloadditions of Phenyl Azide and Cyclooctynes

2. Reactivity and Regioselectivity in 1,3-Dipolar Cycloadditions of Azides to Strained Alkynes and Alkenes: A Computational Study

3. Ring Strain Energy in the Cyclooctyl System. The Effect of Strain Energy on [3 + 2] Cycloaddition Reactions with Azides

4. Ab initio molecular orbital study of conformational properties of cyclohexyne, cycloheptyne, and cyclooctyne

5. 1.3‐Dipolare Cycloadditionen, XXXII. Kinetik der Additionen organischer Azide an CC‐Mehrfachbindungen