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1.
J Org Chem ; 89(15): 10644-10653, 2024 Aug 02.
Artículo en Inglés | MEDLINE | ID: mdl-39012323

RESUMEN

A method for the construction of trifluorinated-5-methylenepyrrolidinone is reported. This strategy combines an acid-catalyzed two-carbon homologation process between ynamides and aldehydes, providing CF3-substituted dienes followed by a metal-free domino hydroamination/isomerization/transamidation sequence, delivering trifluorinated-5-methylenepyrrolidinone stereoselectively.

2.
Chemistry ; 28(1): e202103598, 2022 Jan 03.
Artículo en Inglés | MEDLINE | ID: mdl-34826155

RESUMEN

A copper-mediated coupling reaction between ynamides and diazo-compounds to produce N-allenamides is reported for the first time. This method enables facile and rapid access to terminal N-allenamides by using commercially available TMS-diazomethane with wide functional group compatibility on the nitrogen. Furthermore, the ubiquity of molecules containing a fluorine moiety in medicine, in agricultural, and material science requires the continuous search of new building blocks, including this unique surrogate. The CuI/diazo protocol was successfully applied to the synthesis of fluorine-substituted N-allenamides. DFT calculations provided insights in the mechanism involved.


Asunto(s)
Cobre , Flúor , Compuestos Azo , Catálisis
3.
J Org Chem ; 87(11): 7229-7238, 2022 06 03.
Artículo en Inglés | MEDLINE | ID: mdl-35549261

RESUMEN

A synthesis of new-to-nature aza-iridoids via ynamides is presented. ZrCl4 proved to be the best acid to perform this transformation. Various ynamides were accommodated, and seco-iridoids could be obtained as well. Aza-iridoids were infiltrated into leaves of Scrophularia Nodosa, an iridoid-producing plant species. High-resolution mass spectrometry coupled to computational metabolomic approaches was employed for the detection of aza-iridoid bioconversion products.


Asunto(s)
Iridoides , Scrophularia , Iridoides/química , Espectrometría de Masas , Hojas de la Planta , Scrophularia/química
4.
Sci Adv ; 10(35): eadq3942, 2024 Aug 30.
Artículo en Inglés | MEDLINE | ID: mdl-39196928

RESUMEN

Strigolactones exhibit dual functionality as regulators of plant architecture and signaling molecules in the rhizosphere. The important model crop rice exudes a blend of different strigolactones from its roots. Here, we identify the inaugural noncanonical strigolactone, 4-oxo-methyl carlactonoate (4-oxo-MeCLA), in rice root exudate. Comprehensive, cross-species coexpression analysis allowed us to identify a cytochrome P450, OsCYP706C2, and two methyl transferases as candidate enzymes for this noncanonical rice strigolactone biosynthetic pathway. Heterologous expression in yeast and Nicotiana benthamiana indeed demonstrated the role of these enzymes in the biosynthesis of 4-oxo-MeCLA, which, expectedly, is derived from carlactone as substrate. The oscyp706c2 mutants do not exhibit a tillering phenotype but do have delayed mycorrhizal colonization and altered root phenotype. This work sheds light onto the intricate complexity of strigolactone biosynthesis in rice and delineates its role in symbiosis and development.


Asunto(s)
Lactonas , Oryza , Proteínas de Plantas , Raíces de Plantas , Oryza/genética , Oryza/metabolismo , Lactonas/metabolismo , Proteínas de Plantas/genética , Proteínas de Plantas/metabolismo , Raíces de Plantas/metabolismo , Raíces de Plantas/genética , Vías Biosintéticas , Regulación de la Expresión Génica de las Plantas , Sistema Enzimático del Citocromo P-450/metabolismo , Sistema Enzimático del Citocromo P-450/genética , Mutación , Fenotipo , Micorrizas/metabolismo
5.
Sci Adv ; 9(34): eade8984, 2023 08 25.
Artículo en Inglés | MEDLINE | ID: mdl-37624884

RESUMEN

Specialized metabolite (SM) diversification is a core process to plants' adaptation to diverse ecological niches. Here, we implemented a computational mass spectrometry-based metabolomics approach to exploring SM diversification in tissues of 20 species covering Nicotiana phylogenetics sections. To markedly increase metabolite annotation, we created a large in silico fragmentation database, comprising >1 million structures, and scripts for connecting class prediction to consensus substructures. Together, the approach provides an unprecedented cartography of SM diversity and section-specific innovations in this genus. As a case study and in combination with nuclear magnetic resonance and mass spectrometry imaging, we explored the distribution of N-acylnornicotines, alkaloids predicted to be specific to Repandae allopolyploids, and revealed their prevalence in the genus, albeit at much lower magnitude, as well as a greater structural diversity than previously thought. Together, the data integration approaches provided here should act as a resource for future research in plant SM evolution.


Asunto(s)
Metabolómica , Nicotiana , Nicotiana/genética , Aclimatación , Consenso , Bases de Datos Factuales
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