The chemical nature of the hydrolysis products from the glucosinolate-myrosinase system depends on the presence or absence of supplementary proteins, such as epithiospecifier proteins (ESPs). ESPs (non-catalytic cofactors of myrosinase) promote the formation of epithionitriles from terminal alkenyl glucosinolates and as recent evidence suggests, simple nitriles at the expense of isothiocyanates. The ratio of ESP activity to myrosinase activity is crucial in determining the proportion of these nitriles produced on hydrolysis. Sulphoraphane, a major isothiocyanate produced in broccoli seedlings, has been found to be a potent inducer of phase 2 detoxification enzymes. However, ESP may also support the formation of the non-inductive sulphoraphane nitrile. Our objective was to monitor changes in ESP activity during the development of broccoli seedlings and link these activity changes with myrosinase activity, the level of terminal alkenyl glucosinolates and sulphoraphane nitrile formed. Here, for the first time, we show ESP activity increases up to day 2 after germination before decreasing again to seed activity levels at day 5. These activity changes paralleled changes in myrosinase activity and terminal alkenyl glucosinolate content. There is a significant relationship between ESP activity and the formation of sulforaphane nitrile in broccoli seedlings. The significance of these findings for the health benefits conferred by eating broccoli seedlings is briefly discussed.
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http://dx.doi.org/10.1016/j.phytochem.2008.09.018 | DOI Listing |
J Org Chem
January 2025
Key Laboratory of Biocatalysis & Chiral Drug Synthesis of Guizhou Province, School of Pharmacy, Zunyi Medical University, Zunyi 563003, P. R. China.
A convenient electrochemical oxidative cascade cyclization of alkenes equipped with pendant alcohols with general nucleophiles was developed. Using readily available diarylmethanimine and carboxylic acids as nucleophilic sources, a broad range of internal alkene and terminal alkene substrates could produce RCO- and ArCN-functionalized -heterocycles in moderate to high yields without the requirement for external oxidants and metals. These resulting products can subsequently be hydrolyzed to yield valuable NH- and OH-functionalized tetrahydrofurans and tetrahydropyranes under mild conditions.
View Article and Find Full Text PDFJ Org Chem
January 2025
School of Pharmaceutical Science, Hengyang Medical School, University of South China, Hengyang 421001, Hunan, China.
Although the radical hydroboration of alkenes with N-heterocyclic carbene (NHC) borane is well documented, the radical hydroboration of alkynes, especially terminal alkynes, remains challenging. Herein, a photoredox-catalyzed radical -hydroboration of alkynes with NHC borane has been developed, which provided various alkenyl boron compounds in moderate to good yields. This protocol exhibits a broad substrate scope, as both internal and terminal alkynes were compatible.
View Article and Find Full Text PDFChem Sci
December 2024
Department of Chemistry, Chung-Ang University 84 Heukseok-ro, Dongjak-gu Seoul 06974 Republic of Korea
Recent advancements in eco-friendly radical fluoroalkylation have substituted traditional two-electron-based reactions. However, the radical trifluoromethylation of terminal alkynes remains a significant challenge, primarily due to the high reactivity of alkenyl radical intermediates, which predominantly engage in reactions other than the desired elimination. In this work, we have developed an electrochemical trifluoromethylation method for terminal alkynes, facilitating the efficient formation of CF-alkynes.
View Article and Find Full Text PDFOrg Lett
November 2024
College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao 266042, China.
A photoredox C(sp)-H alkenylation-dehydrogenation of -iodoarylalkanols with terminal alkynes for the synthesis of ()- and ()-quaternary carbon center-containing pent-4-en-1-ones is described. The stereoselectivity depends on the utilization of alkynes and photocatalysts. While using an organic photocatalyst like 4-DPAIPN manipulates the C(sp)-H alkenylation-dehydrogenation of -iodoarylalkanols with arylalkynes to assemble ()-pent-4-en-1-ones, in the case of an Ir potocatalyst such as Ir(ppy)(dtbbpy)PF the reaction with arylalkynes delivers ()-pent-4-en-1-ones.
View Article and Find Full Text PDFChem Commun (Camb)
November 2024
School of Chemistry, Indian Institute of Science Education and Research Thiruvananthapuram, Vithura, Thiruvananthapuram, Kerala 695551, India.
Hydroalkylation of terminal alkynes C-H activation is the most atom-economical and straightforward method for synthesizing alkenes. They remain confined to using C(sp)-H or activated C(sp)-H bonds. A chelating group enabled the alkenylation of C(sp)-H bonds, resulting in alkenes.
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