Divergent synthesis of cyclic ketones via a ring-closing metathesis and oxidation method

Allylation of aldehydes was employed in combination with ring-closing metathesis (RCM) and oxidation reactions to achieve the synthesis of cyclic conjugated ketones. The synthetic strategy involved RCM of the mutual homoallylic alcohol intermediate followed by oxidation reaction to afford the six-me...

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Main Authors: Jorge Cruz-Huerta, Ericka Santacruz, Alejandro Castro, Jorge García-Dávila, Amado Grandes-Blanco
Format: Article
Language:English
Published: Elsevier 2025-01-01
Series:Results in Chemistry
Online Access:http://www.sciencedirect.com/science/article/pii/S2211715624006398
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author Jorge Cruz-Huerta
Ericka Santacruz
Alejandro Castro
Jorge García-Dávila
Amado Grandes-Blanco
author_facet Jorge Cruz-Huerta
Ericka Santacruz
Alejandro Castro
Jorge García-Dávila
Amado Grandes-Blanco
author_sort Jorge Cruz-Huerta
collection DOAJ
description Allylation of aldehydes was employed in combination with ring-closing metathesis (RCM) and oxidation reactions to achieve the synthesis of cyclic conjugated ketones. The synthetic strategy involved RCM of the mutual homoallylic alcohol intermediate followed by oxidation reaction to afford the six-membered cyclic enone. Moreover, when oxidation and RCM were completed successively, the five-membered cyclic enone was obtained.
format Article
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institution Kabale University
issn 2211-7156
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publishDate 2025-01-01
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record_format Article
series Results in Chemistry
spelling doaj-art-157e16b96e5845638219d2f48155a15f2025-01-29T05:00:38ZengElsevierResults in Chemistry2211-71562025-01-0113101943Divergent synthesis of cyclic ketones via a ring-closing metathesis and oxidation methodJorge Cruz-Huerta0Ericka Santacruz1Alejandro Castro2Jorge García-Dávila3Amado Grandes-Blanco4Universidad Politécnica de Tlaxcala, Av. Universidad Politécnica No. 1, San Pedro Xalcatzinco, 90199 Tepeyanco, Tlax., MéxicoUniversidad Politécnica de Tlaxcala, Av. Universidad Politécnica No. 1, San Pedro Xalcatzinco, 90199 Tepeyanco, Tlax., MéxicoUniversidad Politécnica de Tlaxcala, Av. Universidad Politécnica No. 1, San Pedro Xalcatzinco, 90199 Tepeyanco, Tlax., México; Corresponding author.Universidad Politécnica de Tlaxcala, Av. Universidad Politécnica No. 1, San Pedro Xalcatzinco, 90199 Tepeyanco, Tlax., MéxicoUniversidad Autónoma de Tlaxcala, Ribereña S/N, Centro, 90000 Tlaxcala, Tlax., MéxicoAllylation of aldehydes was employed in combination with ring-closing metathesis (RCM) and oxidation reactions to achieve the synthesis of cyclic conjugated ketones. The synthetic strategy involved RCM of the mutual homoallylic alcohol intermediate followed by oxidation reaction to afford the six-membered cyclic enone. Moreover, when oxidation and RCM were completed successively, the five-membered cyclic enone was obtained.http://www.sciencedirect.com/science/article/pii/S2211715624006398
spellingShingle Jorge Cruz-Huerta
Ericka Santacruz
Alejandro Castro
Jorge García-Dávila
Amado Grandes-Blanco
Divergent synthesis of cyclic ketones via a ring-closing metathesis and oxidation method
Results in Chemistry
title Divergent synthesis of cyclic ketones via a ring-closing metathesis and oxidation method
title_full Divergent synthesis of cyclic ketones via a ring-closing metathesis and oxidation method
title_fullStr Divergent synthesis of cyclic ketones via a ring-closing metathesis and oxidation method
title_full_unstemmed Divergent synthesis of cyclic ketones via a ring-closing metathesis and oxidation method
title_short Divergent synthesis of cyclic ketones via a ring-closing metathesis and oxidation method
title_sort divergent synthesis of cyclic ketones via a ring closing metathesis and oxidation method
url http://www.sciencedirect.com/science/article/pii/S2211715624006398
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