A DFT study on the Sc(OTf)3 catalyzed hetero Diels–Alder reaction of N-tosylhydrazones and ortho-quinone methides: energetic aspects, selectivities, and molecular mechanism-Reference-Cited by-同舟云学术

A DFT study on the Sc(OTf)3 catalyzed hetero Diels–Alder reaction of N-tosylhydrazones and ortho-quinone methides: energetic aspects, selectivities, and molecular mechanism

Published:2023-07-06 Issue: Volume: Page:
ISSN:1040-0400
Container-title:Structural Chemistry
language:en
Short-container-title:Struct Chem

Author:

Soleymani Mousa^ORCID,Goudarzi Mahdieh

Funder

Ayatollah Boroujerdi University

Publisher

Springer Science and Business Media LLC

Subject

Physical and Theoretical Chemistry,Condensed Matter Physics

Link

https://link.springer.com/content/pdf/10.1007/s11224-023-02201-4.pdf

Reference44 articles.

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3. Domingo LR, Arnó M, Andrés J (1999) Influence of reactant polarity on the course of the inverse-electron-demand Diels− Alder reaction. A DFT study of regio-and stereoselectivity, presence of Lewis Acid catalyst, and inclusion of solvent effects in the reaction between nitroethene and substituted ethenes. J Org Chem 64:5867–5875

4. Emamian S, Soleymani M, Moosavi SS (2019) Copper (i)-catalyzed asymmetric aza Diels-Alder reactions of azoalkenes toward fulvenes: a molecular electron density theory study. New J Chem 43:4765–4776

5. Soleymani M, Chegeni M, Mohammadi E (2021) BF3-catalyzed oxa-Diels–Alder reaction of ethyl vinyl sulfide and β-methyl-α-phenylacrolein: a molecular electron density theory study. Monatsh Chem Chem Mon 152:1209–1221

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