Dipolar 1,3‐cycloaddition of thioformaldehyde S ‐methylide ( <scp> CH 2 SCH 2 </scp> ) to ethylene and acetylene. A comparison with (valence) isoelectronic <scp> O 3 </scp> , <scp> SO 2 </scp> , <scp> CH 2 OO </scp> and <scp> CH 2 SO </scp>-Reference-Cited by-同舟云学术

Dipolar 1,3‐cycloaddition of thioformaldehyde S ‐methylide ( CH ₂ SCH ₂ ) to ethylene and acetylene. A comparison with (valence) isoelectronic O ₃ , SO ₂ , CH ₂ OO and CH ₂ SO

Published:2022-06-06 Issue:21 Volume:43 Page:1420-1433
ISSN:0192-8651
Container-title:Journal of Computational Chemistry
language:en
Short-container-title:J Comput Chem

Author:

Salta Zoi¹^ORCID,Vega‐Teijido Mauricio²^ORCID,Katz Aline²^ORCID,Tasinato Nicola¹^ORCID,Barone Vincenzo¹^ORCID,Ventura Oscar N.²^ORCID

Affiliation:

1. SMART Lab Scuola Normale Superiore Pisa Italy

2. Computational Chemistry and Biology Group, CCBG, DETEMA, Facultad de Química Universidad de la República Montevideo Uruguay

Funder

Scuola Normale Superiore

Publisher

Wiley

Subject

Computational Mathematics,General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcc.26946

Reference112 articles.

1. The first two-step 1,3-dipolar cycloadditions: non-stereospecificity

2. Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products

3. 1,3-Dipolar cycloadditions. 76. Concerted nature of 1,3-dipolar cycloadditions and the question of diradical intermediates

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