35122-96-4Relevant articles and documents
Halogen bonding-enhanced electrochemical halide anion sensing by redox-active ferrocene receptors
Lim, Jason Y. C.,Cunningham, Matthew J.,Davis, Jason J.,Beer, Paul D.
, p. 14640 - 14643 (2015)
The first examples of halogen bonding redox-active ferrocene receptors and their anion electrochemical sensing properties are reported. Halogen bonding was found to significantly amplify the magnitude of the receptor's metallocene redox-couple's voltammet
Reduction-rebridging strategy for the preparation of ADPN-based antibody-drug conjugates
Koniev, Oleksandr,Dovgan, Igor,Renoux, Brigitte,Ehkirch, Anthony,Eberova, Jitka,Cianférani, Sarah,Kolodych, Sergii,Papot, Sébastien,Wagner, Alain
supporting information, p. 827 - 830 (2018/05/31)
The reduction-rebridging strategy is a powerful method for the preparation of stable and homogeneous antibody-drug conjugates (ADCs). In this communication, we describe the development of the arylene-dipropiolonitrile (ADPN) functional group for the rebri
3,5-diiodo benzenesulfonyl choride preparation technology
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Paragraph 0007; 0046; 0078; 0084; 0085, (2018/01/09)
The invention discloses a 3,5-diiodo benzenesulfonyl choride preparation technology. The preparation technology comprises the following steps: taking paranitroaniline as a raw material, performing a substitution reaction to generate 2,6-diiodo-4-nitro aniline, performing diazotization and hydrolysis on 2,6-diiodo-4-nitro aniline and performing hydrolysis to generate 3,5-diodonitrobenzene, performing a reduction reaction on the 3,5-diodonitrobenzene to generate 3,5-diiodoaniline, performing diazotization and a sulfonylation reaction on the 3,5-diiodoaniline to obtain a target compound 3,5-diiodo benzenesulfonyl choride. The technology has the advantages of easily available raw materials, simple operation and post-treatment, and high yield, and is suitable for industrial production.
MICROBUBBLE-CHEMOTHERAPEUTIC AGENT COMPLEX FOR SONODYNAMIC THERAPY
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Page/Page column 57; 58, (2017/06/29)
The invention relates to methods of sonodynamic therapy comprising the co-administration of a microbubble-chemotherapeutic agent complex together with a microbubble-sonosensitiser complex. It further relates to pharmaceutical compositions comprising these
A Pronounced Halogen Effect on the Organogelation Properties of Peripherally Halogen Functionalized Poly(benzyl ether) Dendrons
Feng, Yu,Chen, Hui,Liu, Zhi-Xiong,He, Yan-Mei,Fan, Qing-Hua
, p. 4980 - 4990 (2016/04/05)
An interesting halogen-substituent effect on the organogelation properties of poly(benzyl ether) dendrons is reported. A new class of poly(benzyl ether) dendrons with halo substituents decorating their periphery was synthesized and fully characterized. A
Synthesis and optoelectronic properties of janus -dendrimer-type multivalent donor-acceptor systems
Dengiz, Cagatay,Breiten, Benjamin,Gisselbrecht, Jean-Paul,Boudon, Corinne,Trapp, Nils,Schweizer, W. Bernd,Diederich, Fran?ois
, p. 882 - 896 (2015/01/30)
A convergent, multistep protocol was employed for the synthesis of a Janus-type multivalent donor-acceptor system. The synthetic approach is based on a Sonogashira cross-coupling of two differently ferrocene-(Fc) substituted dendrons and a final sixfold [
Iron(III) complexes with meta-substituted bis(arylimino)pyridine ligands: Catalyst precursors for the selective oligomerization of ethylene
G?rl, Christian,Beck, Nadine,Kleiber, Katharina,Alt, Helmut G.
experimental part, p. 110 - 127 (2012/02/02)
Bis(arylimino)pyridine iron(III) complexes containing meta-halogen substituents at the iminophenyl rings were synthesized and characterized. In contrast to iron(II) complexes, the presence of at least one ortho-substituent at the iminophenyl rings is not obligative for catalytic activities of these iron(III) complexes. After activation with methylaluminoxane (MAO), these catalysts oligomerize ethylene to give also internal and branched olefins besides the expected linear α-olefins. The widths of the resulting molecular weight distributions and the degrees of isomerization of the resulting oligomers strongly depend on the substitution pattern at the ligand frameworks.
Leukotriene B4 Inhibitors
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Page/Page column 64, (2009/04/24)
Provided herein are compounds of the formula (I): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful for the treatment of diseases such as, for example, COPD
ANTIBACTERIAL COMPOSITIONS
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Page/Page column 22-23, (2008/06/13)
Compounds of formula (I) have antibacterial activity: wherein: m is 0 or 1 ; Q is hydrogen or cyclopropyl; AIk is an optionally substituted, divalent C1-C6 alkylene, alkenylene or alkynylene radical which may contain an ether (-O-), thioether (-S-) or amino (-NR)- link, wherein R is hydrogen, -CN or C1-C3 alkyl; X is -C(=O)NR6-, -S(O)NR6-, -C(=O)O- or -S(=O)O- wherein R6 is hydrogen, optionally substituted C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, -Cyc, or -( C1-C3 alkyl)-Cyc wherein Cyc is optionally substituted monocyclic carbocyclic or heterocyclic having 3-7 ring atoms; Z is N or CH, or CF; R2 and R3 are as defined in the description.
Synthesis of new diethynylbenzene derivatives
Chimenti,Bolasco,Secci,Chimenti,Granese
, p. 2549 - 2555 (2007/10/03)
The preparation of new monomeric diacetylenic aromatic compounds is described.