para -Quinone Methides as Acceptors in 1,6-Nucleophilic Conjugate Addition Reactions for the Synthesis of Structurally Diverse Molecules-Reference-Cited by-同舟云学术

para -Quinone Methides as Acceptors in 1,6-Nucleophilic Conjugate Addition Reactions for the Synthesis of Structurally Diverse Molecules

Published:2020-03-31 Issue:18 Volume:2020 Page:2650-2692
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Lima Carolina G. S.¹,Pauli Fernanda P.¹,Costa Dora C. S.¹,de Souza Acácio S.¹,Forezi Luana S. M.¹,Ferreira Vitor F.²,de Carvalho da Silva Fernando¹^ORCID

Affiliation:

1. Departamento de Química Orgânica; Instituto de Química; Universidade Federal Fluminense; Campus do Valonguinho 24020-150 Niterói RJ Brazil

2. Departamento de Tecnologia Farmacêutica; Universidade Federal Fluminense; 24241-000 Niterói RJ Brazil

Funder

Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro

Fundação de Apoio ao Ensino, Pesquisa e Assistência do Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201901796/fullpdf

Reference216 articles.

1. Catecholamine Chemical Species at the Adrenergic Receptors

2. Ferrocenyl Quinone Methides as Strong Antiproliferative Agents: Formation by Metabolic and Chemical Oxidation of Ferrocenyl Phenols

3. Ferrocenyl Quinone Methides as Strong Antiproliferative Agents: Formation by Metabolic and Chemical Oxidation of Ferrocenyl Phenols

4. Biosynthesis of antimalarial lignans from Holostylis reniformis

5. Molecular Basis of Elansolid Biosynthesis: Evidence for an Unprecedented Quinone Methide Initiated Intramolecular Diels-Alder Cycloaddition/Macrolactonization

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