Results 11 to 20 of about 1,283 (179)

Thiocarbamate

open access: yesZeitschrift für Naturforschung B, 1955
Rhodanide und konz. Schwefelsäure reagieren unter Bildung von Estern miteinander, deren Hydrolyse zu Monothiocarbamidsäure-S-R-estern (Thiocarbamaten) führt.
R. Riemschneider, O. Lorenz
openaire   +1 more source

Thiocarbamates as plant growth regulators [PDF]

open access: yesPlant Physiology, 1961
The findings of van der Kerk and his coworkers (10) that carboxymethyl (limietlhyldithiocarbamate (1) caused epinastic curvature ancl leaf deformations as well as some elongation of Avena coleoptile tissue related its action as a growth regulator to that of indole-3-acetic acid and other aromatic structures.
R M, Muir, C, Hansch, J, Gally
openaire   +2 more sources

N-(4-Bromophenyl)methoxycarbothioamide

open access: yesMolbank, 2018
The synthesis, spectroscopic and crystallographic characterisation of the title compound, O-methyl-N-4-bromophenyl thiocarbamate, MeOC(=S)N(H)PhBr-4 (1), are described.
Chien Ing Yeo, Edward R.T. Tiekink
doaj   +1 more source

Pesticide Toxicity Profile: Thiocarbamate Fungicides

open access: yesEDIS, 2005
This document provides a general overview of human toxicity, provides a listing of laboratory animal and wildlife toxicities and a cross reference of chemical, common and trade names of thiocarbamate pesticides used as fungicides registered for use in ...
Frederick M. Fishel
doaj   +5 more sources

Structure-guided engineering of molinate hydrolase for the degradation of thiocarbamate pesticides.

open access: yesPLoS ONE, 2015
Molinate is a recalcitrant thiocarbamate used to control grass weeds in rice fields. The recently described molinate hydrolase, from Gulosibacter molinativorax ON4T, plays a key role in the only known molinate degradation pathway ending in the formation ...
José P Leite   +6 more
doaj   +1 more source

Novel Cholinesterase Inhibitors Based on O-Aromatic N,N-Disubstituted Carbamates and Thiocarbamates

open access: yesMolecules, 2016
Based on the presence of carbamoyl moiety, twenty salicylanilide N,N-disubstituted (thio)carbamates were investigated using Ellman’s method for their ability to inhibit acetylcholinesterase (AChE) and butyrylcholinesterase (BChE).
Martin Krátký   +4 more
doaj   +1 more source

Reasoned opinion on the modification of the existing MRL(s) for prosulfocarb in fennel [PDF]

open access: yesEFSA Journal, 2013
In accordance with Article 6 of Regulation (EC) No 396/2005, Belgium, hereafter referred to as the evaluating Member State (EMS), compiled an application to modify the existing MRL for the active substance prosulfocarb in fennel.
European Food Safety Authority
doaj   +1 more source

A novel three-component reaction between isocyanides, alcohols or thiols and elemental sulfur: a mild, catalyst-free approach towards O-thiocarbamates and dithiocarbamates

open access: yesBeilstein Journal of Organic Chemistry, 2019
A new multicomponent reaction has been developed between isocyanides, sulfur and alcohols or thiols under mild reaction conditions to afford O-thiocarbamates and dithiocarbamates in moderate to good yields.
András György Németh   +2 more
doaj   +1 more source

A non-solvated form of [(Z)-O-methyl-N-(2-methylphenyl)thiocarbamato-κS](triphenylphosphane-κP)gold(I): crystal structure and Hirshfeld surface analysis

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2016
The title compound, [Au(C9H10NOS)(C18H15P)], features a near linear P—Au—S arrangement defined by phosphane P and thiolate S atoms with the minor distortion from the ideal [P—Au—S is 177.61 (2)°] being traced in part to the close intramolecular approach ...
Chien Ing Yeo   +2 more
doaj   +1 more source

Synthesis of Secondary Amides from Thiocarbamates [PDF]

open access: yesOrganic Letters, 2018
The synthesis of secondary amides from readily accessible and bench-stable substituted S-phenyl thiocarbamates and Grignard reactants is reported. Oxidative workup allows recycling of the thiolate leaving group as diphenyl disulfide. Diphenyl disulfide can be transformed into S-phenyl benzenethiosulfonate, a reactant required for thiocarbamate ...
Pieter Mampuys   +3 more
openaire   +3 more sources

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