17243-13-9Relevant academic research and scientific papers
PESTICIDALLY ACTIVE HETEROCYCLIC DERIVATIVES WITH SULFUR CONTAINING SUBSTITUENTS
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Page/Page column 105; 108, (2022/03/22)
Compounds of the formula (I) wherein G1, G2, X, R2 and Q are as defined in claim 1. Furthermore, the present invention relates to agrochemical compositions which comprise compounds of formula (I), to preparation of these compositions, and to the use of the compounds or compositions in agriculture or horticulture for combating, preventing or controlling animal pests, including arthropods and in particular insects, molluscs, nematodes or representatives of the order Acarina.
Rare earth centered hybrid materials: Tb3+ covalently bonded with La3+, Gd3+, Y3+ through sulfonamide bridge and luminescence enhancement
Sheng, Kai,Yan, Bing,Qiao, Xiao-Fei
experimental part, p. 653 - 662 (2012/05/05)
The organic ligand 5-sulfosalicylic acid (SSA) is grafted by (3-aminopropyl) triethoxysilane (APTES) to achieve functionalized sulfonamide bridge (SSA-Si) which can both coordinate to Ln3+ to form luminescent center and link inorganic Si-O netw
Lanthanide/zinc centered photoactive hybrids with functional sulfonamide linkage: Coordination bonding assembly, characterization and photophysical properties
Qian, Kai,Yan, Bing
experimental part, p. 226 - 231 (2010/04/04)
In this paper, two novel kinds of organic-inorganic monomer, SUA-APEMS and SUA-APS, have been achieved by modifying 5-sulfosalicylic acid (SUA) with 3-aminopropyl-methyl-diethoxylsilane (APEMS) and 3-aminopropyl trimethoxysilane (APS). These two organic-i
NOVEL PROCESS FOR THE PREPARATION OF SILDENAFIL CITRATE
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Page/Page column 6; 11, (2008/06/13)
Disclosed herein the process for producing 5-[2-ethoxy-5-(4-methyl)piperazine-l-yl- sulfonyl)phenyl]- 1 -methyl-3-n-propyl- 1 ,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one or its salt thereof employing novel intermediate.
Substituted phenyl methanone derivatives
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Page/Page column 11, (2008/06/13)
The present invention relates to compounds of formula I wherein R1, R2, R3, n, and m, are as defined in the specification and to pharmaceutically acceptable acid addition salts thereof. These compounds are good inhibitors
[4-(HETEROARYL) PIPERAZIN-1-YL]-(2,5-SUBSTITUTED -PHENYL)METHANONE DERIVATIVES AS GLYCINE TRANSPORTER 1 (GLYT-1) INHIBITORS FOR THE TREATMENT OF NEUROLOGICAL AND NEUROPSYCHIATRIC DISORDERS
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Page/Page column 31, (2008/06/13)
The present invention relates to compounds of the general formula (I) wherein R1 is-OR1’,-SR1’ or is a heterocycloalkyl group; R1’ is lower alkyl, lower alkyl substituted by halogen or is -(CH2)n
Heterocyclic-substituted phenyl methanones
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Page/Page column 67, (2008/06/13)
The present invention relates to compounds of formula I wherein R1, R2, and are defined in the specification and to pharmaceutically acceptable acid addition salts thereof.
SODIUM BOROHYDRIDE REDUCTION OF AROMATIC SULFONYL AZIDES IN THE PRESENCE OR ABSENCE OF TELLURIUM
Obafemi, Craig. A.,Onigbinde, Adebayo O.
, p. 75 - 81 (2007/10/02)
Some aromatic sulfonyl azides have been reduced, in various solvents, with sodium borohydride, in the presence or absence of Te element to the corresponding sulfonamides.Other functionals groups like the imino group may also be reduced.
Novel 5-alkylsulfonylsalicylanilides and microbiocidal compositions for controlling the growth of microorganisms
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, (2008/06/13)
This invention relates to new 5-alkylsulfonylsalicylanilides and methods for their use. More particularly, the invention relates to compounds of the formula: STR1 Wherein Z is a substituted or unsubstituted phenyl ring of from 6 to 30 carbon atoms includi
