Disclosed is a method for producing a trisulfide compound or a selenotrisulfide compound. This production method includes: a step for oxidizing a disulfide compound with an oxidizing agent to obtain a sulfoxide compound; and a step for reacting the sulfoxide compound that has been obtained with a source of sulfur or a source of selenium to obtain a trisulfide compound or a selenotrisulfide compound.

Disclosed is a method for producing a trisulfide compound or a selenotrisulfide compound. This production method includes: a step for oxidizing a disulfide compound with an oxidizing agent to obtain a sulfoxide compound; and a step for reacting the sulfoxide compound that has been obtained with a source of sulfur or a source of selenium to obtain a trisulfide compound or a selenotrisulfide compound.

This disclosure relates to the field of molecules having pesticidal utility against pests in Phyla Arthropoda, Mollusca, and Nematoda, processes to produce such molecules, intermediates used in such processes, pesticidal compositions containing such molecules, and processes of using such pesticidal compositions against such pests. These pesticidal compositions may be used, for example, as acaricides, insecticides, miticides, molluscicides, and nematicides. This document discloses molecules having the following formula (“Formula One”).

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This disclosure relates to the field of molecules having pesticidal utility against pests in Phyla Arthropoda, Mollusca, and Nematoda, processes to produce such molecules, intermediates used in such processes, pesticidal compositions containing such molecules, and processes of using such pesticidal compositions against such pests. These pesticidal compositions may be used, for example, as acaricides, insecticides, miticides, molluscicides, and nematicides. This document discloses molecules having the following formula (“Formula One”).

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An effective process of making N,N′-diacetyl-L-Cystine (“NDAC”), which process is fast, green, does not require labor-intensive isolation or purification of the product, by yielding products in desired ratio, and has improved yield and purity. The process comprising the steps of Forming a reaction mixture, starting with a cystine derivative di-tert- butyl-L-cystine as the dihydrochloride form; Acetylating said di-tert-butyl-L-cystine to obtain N,N′-diacetyl-di-tert- butyl-L-cystine; followed by Removing said tert- butyl groups from said N,N′-diacetyl-di-tert-butyl- L-cystine to obtain N,N′-diacetyl-L-cystine product; and Isolating said N,N′-diacetyl-L-Cystine product from said reaction mixture; wherein said acetylating agent is acetic anhydride.

An effective process of making N,N′-diacetyl-L-Cystine (“NDAC”), which process is fast, green, does not require labor-intensive isolation or purification of the product, by yielding products in desired ratio, and has improved yield and purity. The process comprising the steps of Forming a reaction mixture, starting with a cystine derivative di-tert- butyl-L-cystine as the dihydrochloride form; Acetylating said di-tert-butyl-L-cystine to obtain N,N′-diacetyl-di-tert- butyl-L-cystine; followed by Removing said tert- butyl groups from said N,N′-diacetyl-di-tert-butyl- L-cystine to obtain N,N′-diacetyl-L-cystine product; and Isolating said N,N′-diacetyl-L-Cystine product from said reaction mixture; wherein said acetylating agent is acetic anhydride.

An effective process of making N,N′-diacetyl-L-Cystine (“NDAC”), which process is fast, green, does not require labor-intensive isolation or purification of the product, by yielding products in desired ratio, and has improved yield and purity. The process comprising the steps of Forming a reaction mixture, starting with a cystine derivative di-tert- butyl-L-cystine as the dihydrochloride form; Acetylating said di-tert-butyl-L-cystine to obtain N,N′-diacetyl-di-tert- butyl-L-cystine; followed by Removing said tert- butyl groups from said N,N′-diacetyl-di-tert-butyl- L-cystine to obtain N,N′-diacetyl-L-cystine product; and Isolating said N,N′-diacetyl-L-Cystine product from said reaction mixture; wherein said acetylating agent is acetic anhydride.

Provided are a protein antigen subjected to site-directed mutation and site-directed modification, and a method for site-directed mutation and site-directed modification of the protein antigen. The method comprises: site-directedly introducing an unnatural amino acid into a specific site of the protein antigen by genetic codon expansion technique; and performing site-directed modification with the protein antigen by the unnatural amino acid and a modifier, wherein the modifier is a receptor agonist such as tripalmitoyl-S-glyceryl cysteine and monophosphoryl lipid A. Further provided is use of the protein antigen subjected to site-directed mutation and site-directed modification, such as use as a vaccine.

The present invention relates to a method of preparing N-acyl amino acids selected from N-acyl cysteine compounds, N-acyl serine compounds, N-acyl aspartic acid compounds and N-acyl glutamic acid compounds. The present invention also relates to the use of N-acyl cysteine, N-acyl serine, N-acyl aspartic acid and N-acyl glutamic acid surfactants, in removing per- and poly-fluoroalkyl substances (PFASs) from mixtures containing PFASs, such as soil and groundwater contaminated with PFASs and for use in cleaning compositions, detergent compositions and toothpaste compositions.

The present invention relates to a method of preparing N-acyl amino acids selected from N-acyl cysteine compounds, N-acyl serine compounds, N-acyl aspartic acid compounds and N-acyl glutamic acid compounds. The present invention also relates to the use of N-acyl cysteine, N-acyl serine, N-acyl aspartic acid and N-acyl glutamic acid surfactants, in removing per- and poly-fluoroalkyl substances (PFASs) from mixtures containing PFASs, such as soil and groundwater contaminated with PFASs and for use in cleaning compositions, detergent compositions and toothpaste compositions.