Product selectivity in the photoreaction of aryl sulfonates and mesylate of estrone derivatives in sustainable and micellar media: a steady-state investigation-Reference-Cited by-同舟云学术

Product selectivity in the photoreaction of aryl sulfonates and mesylate of estrone derivatives in sustainable and micellar media: a steady-state investigation

Published:2022 Issue:32 Volume:46 Page:15504-15520
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Quindt Matías I.¹²,Gola Gabriel F.¹³,Rodriguez Cristian R.¹³,Ramirez Javier A.¹³^ORCID,Bonesi Sergio M.¹²^ORCID

Affiliation:

1. Universidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Departamento de Química Orgánica, Buenos Aires, Argentina

2. CONICET–Universidad de Buenos Aires, Centro de Investigaciones en Hidratos de Carbono (CIHIDECAR), Buenos Aires, Argentina

3. CONICET–Universidad de Buenos Aires, Unidad de Microanálisis y Métodos Físicos Aplicados a Química Orgánica (UMYMFOR), Buenos Aires, Argentina

Abstract

The photochemical reaction of sulfonate steroids in a sustainable environment was carried out successfully under steady-state conditions. Significant selectivity in photoproduct formation was also observed.

Funder

Consejo Nacional de Investigaciones Científicas y Técnicas

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2022/NJ/D2NJ02989H

Reference89 articles.

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2. Synthesis of 4-Formyl Estrone Using a Positional Protecting Group and Its Conversion to Other C-4-Substituted Estrogens

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4. Inhibitors of type 1 17β-hydroxysteroid dehydrogenase with reduced estrogenic activity: Modifications of the positions 3 and 6 of estradiol

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