Aromaticity of Cope and Claisen rearrangements-Reference-Cited by-同舟云学术

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Aromaticity of Cope and Claisen rearrangements

Published:2023-04-13 Issue:5 Volume:142 Page:
ISSN:1432-881X
Container-title:Theoretical Chemistry Accounts
language:en
Short-container-title:Theor Chem Acc

Author:

Castro Thiago S.,Martins Guilherme F.,de Alcântara Morais Sara F.,Ferreira Daví A. C.

Funder

CAPES

Conselho Nacional de Desenvolvimento Científico e Tecnológico

SESu/MEC/PETQuímica-UnB

Publisher

Springer Science and Business Media LLC

Subject

Physical and Theoretical Chemistry

Link

https://link.springer.com/content/pdf/10.1007/s00214-023-02975-0.pdf

Reference52 articles.

1. Woodward RB, Hoffmann R (1969) The conservation of orbital symmetry. Angew Chem Int Ed Engl 8:781–853. https://doi.org/10.1002/anie.196907811

2. Cope AC, Hardy EM (1940) The introduction of substituted vinyl groups. V. A rearrangement involving the migration of an allyl group in a three-carbon system1. J Am Chem Soc 62:441–444. https://doi.org/10.1021/ja01859a055

3. Claisen L (1912) Über Umlagerung von Phenol-allyläthern in C-Allyl-phenole. Ber Dtsch Chem Ges 45:3157–3166. https://doi.org/10.1002/cber.19120450348

4. Ilardi EA, Stivala CE, Zakarian A (2009) [3,3]-Sigmatropic rearrangements: recent applications in the total synthesis of natural products. Chem Soc Rev 38:3133–3148. https://doi.org/10.1039/B901177N

5. Nowicki J (2000) Claisen, Cope and related rearrangements in the synthesis of flavour and fragrance compounds. Molecules 5:1033–1050

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3. Chiral cobalt(ii) complex-promoted asymmetric para-Claisen rearrangement of allyl α-naphthol ethers;Chemical Science;2023

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