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To explore and utilize the abundant soil microorganisms and their beneficial functions, high-throughput sequencing technology was used to analyze soil microbial compositions in the rhizosphere of red and green amaranth varieties. The results showed that significant differences in soil microbial composition could be found in the rhizosphere of amaranth plants with different color phenotypes. Firstly, soil bacterial compositions in the rhizosphere were significantly different between red and green amaranths. Among them, Streptomyces, Pseudonocardia, Pseudolabrys, Acidibacter, norank_ f_ Micropepsaceae, Bradyrhizobium, and Nocardioides were the unique dominant soil bacterial genera in the rhizosphere of red amaranth. In contrast, Conexibacter, norank_f_norank_o_norank_c_TK10, and norank_f_ norank_o_ norank_ c_AD3 were the special dominant soil bacterial genera in the rhizosphere of green amaranth. Additionally, even though the soil fungal compositions in the rhizosphere were not significantly different between red and green amaranths, the abundance of the dominant soil fungal genera in the rhizosphere showed significant differences between red and green amaranths. For example, unclassified_k__Fungi, Fusarium, Cladophialophora, unclassified_c__Sordariomycetes and unclassified_p__Chytridiomycota significantly enriched as the dominant soil fungal genera in the rhizosphere of the red amaranth. In contrast, Aspergillues only significantly enriched as the dominant soil fungal genus in the rhizosphere of green amaranth. All of the above results indicated that amaranth with various color phenotypes exactly recruited different microorganisms in rhizosphere, and the enrichments of soil microorganisms in the rhizosphere could be speculated in contributing to amaranth color formations. [ABSTRACT FROM AUTHOR]

This document provides a detailed overview of the synthesis and characterization of β-hydroxyhydrophosphonic acids and their derivatives. The traditional methods for synthesizing these compounds have limitations, and the article presents a new method that uses sodium hypophosphite as a green and cost-effective phosphorus source. The reaction is catalyzed by silver trifluoromethanesulfonate and demonstrates good efficiency and functional group compatibility. The document includes information on the chemical properties of various phosphinic acids, providing data such as NMR spectra, melting points, and yields for each compound. This information can be valuable for researchers studying these compounds and their properties. [Extracted from the article]

Transition‐metal‐catalyzed coupling reactions that involve the direct functionalization of insert C−H bond represent one of the most efficient strategies for forming carbon‐carbon bonds. Herein, a palladium‐catalyzed intramolecular C−H bond arylation of triaryl phosphates is reported to access seven‐membered cyclic biarylphosphonate targets. The reaction is achieved via a unique eight‐membered palladacyclic intermediate and shows good functional group compatibility. Meanwhile, the product can be readily converted into other valuable phosphate compounds. [ABSTRACT FROM AUTHOR]

A metal-free method for the dual activation of aryl phosphinate has been developed; the P–H and P–O bonds are sequentially activated by the Tf2O/DMSO system. Without the requirement of metals and unstable P-reagents, this one-pot procedure provides a convenient and practical access to a variety of aryl phosphonates. A mechanism involving twice generation of electrophilic P-species and two SN-processes is proposed on the basis of the control experiments. [ABSTRACT FROM AUTHOR]

Herein, metal-free phosphonation of N-heterocycles with diphenylphosphine oxides, promoted by easily available 1,5-diazabicyclo[5,4,0]undec-5-ene (DBU) in dimethyl carbonate (DMC) as a green solvent under an air atmosphere, is presented. This simple method can accommodate 1,2,4-triazine-3,5(2H,4H)-diones, quinoxalin-2(1H)-ones, quinoxalines and pyrazinones with diverse substituted diphenylphosphine oxides, delivering distinctive monophosphonated N-heterocycles with a broad functional group tolerance, and the transformations are also viable for post-modification of bioactive and pharmaceutical molecules. In addition to the sustainable feature of being metal- and photocatalyst-free and utilization of ambient air as an oxidant, this method efficiently achieves the gram-scale transformation, and the product was isolated through extraction and filtration, rather than column chromatography. [ABSTRACT FROM AUTHOR]

We have developed a simple and effective method for the C-3 arylation of phosphorus-containing indole compounds in the presence of CuI under mild conditions. This reaction provides a reliable method for the modification of ligands. [ABSTRACT FROM AUTHOR]