Results 121 to 130 of about 14,696 (253)

EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids (CEF); Scientific Opinion on Flavouring Group Evaluation 17, Revision 3 (FGE.17Rev3): Pyrazine derivatives from chemical group 24 [PDF]

, 2011
Aeschbacher, Ajimu, Ajimu, Anderson, Babish, Beedham, Beedham, Beedham, Beutin, Burdock, Béraud, Cashman, Cashman, Cashman, Cashman, Cramer, D'Souza, Damani, Damani, Damani, Dutton, EC, EC, EC, EC, EC, EFFA, EFFA, Elfarra, Epler, Fung, Galloway, Hashimoto, Hawksworth, Hogben, Hoodi, IOFI, JECFA, JECFA, Knize, Koyama, Lee, Liang, Maiorino, McBain, McMahon, Moran, Nickson, Nickson, Nnane, Novotny, Oser, Oser, Oser, Oser, Oser, Parkinson, Posternak, Posternak, Rettie, Richardson, Rosenkranz, Roure Inc., Sadeque, Sadeque, SCF, Schranker, Sjödin, Stich, Stubley, Stubley, Sullivan, TNO, TNO, TNO, Topham, Tsai, Turesky, Vollmuth, Wallin, Whitehouse, Wild, Williams, Yamada, Yamada, Yamada, Yamamoto, Yamamoto, Yoshihara, Zeiger, Ziegler   +90 more
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Preparation of atomic oxygen resistant polymeric materials [PDF]

Polyphenyl quinoxalines (PPQs) are an important family of high performance polymers that offer good chemical and thermal stability coupled with excellent mechanical properties.
Connell, J. W., Hergenrother, P. M., Tortorelli, Victor J.   +2 more
core   +1 more source

On the Nitration of Quinoxalines (Addendum)

, 1960
Hirotaka Otomasu, Kei Yoshida
openalex   +2 more sources

6,7-Dichloro-2,3-bis(pyridin-2-yl)quinoxaline [PDF]

, 2015
Guy Crundwell, Neil M. Glagovich, Melissa E. King   +2 more
openalex   +1 more source

Data from Targeting the NF-κB and mTOR Pathways with a Quinoxaline Urea Analog That Inhibits IKKβ for Pancreas Cancer Therapy

, 2023
Prakash Radhakrishnan, Vashti C. Bryant, Elizabeth C. Blowers, Rajkumar N. Rajule, Nagsen Gautam, Muhammad M. Anwar, Ashley M. Mohr, Paul M. Grandgenett, Stephanie K. Bunt, Jamie L. Arnst, Subodh M. Lele, Yazen Alnouti, Michael A. Hollingsworth, Amarnath Natarajan   +13 more
openalex   +1 more source

SYNTHESIS, REACTIVITY AND BIOLOGICAL ACTIVITY OF QUINOXALIN-2-ONE DERIVATIVES

Scientific Study & Research: Chemistry & Chemical Engineering, Biotechnology, Food Industry, 2010
Quinoxalines have a great interest in various fields and particularly in chemistry, biology and pharmacology. It enabled the researchers to develop many methods for their preparations and to seek new fields of application.
El Mokhtar Essassi, R. Bouhfid, Y. Kandri Rodi, S. Ferfra, H. Benzeid, Y. Ramli   +5 more
doaj  

Effect of molecular weight on polyphenylquinoxaline properties [PDF]

A series of polyphenyl quinoxalines with different molecular weight and end-groups were prepared by varying monomer stoichiometry. Thus, 4,4'-oxydibenzil and 3,3'-diaminobenzidine were reacted in a 50/50 mixture of m-cresol and xylenes.
Jensen, Brian J.
core   +1 more source

Generality and Scope of the Synthesis of 2-Arylpyrrolo[3,4-b]quinoxaline-1,3-diones from 2,3-Dichloro-N-arylmaleimides. II

, 1999
Leila Hanaineh‐Abdelnour, Badr A. Salameh   +1 more
openalex   +1 more source

Variation of Skeletons of Antitumor Antibiotics. II. Synthesis of Naphtho-[2, 3-g] quinolines and Naphtho [2, 3-g] quinoxalines

, 1981
Kazuhiro Kobayashi, NORIICHI ODA, ISOO ITO   +2 more
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SYNTHESIS, CHARACTERIZATION AND ANTIBACTERIAL EVALUATION OF FEW 2, 3-SUBSTITUTED QUINOXALINES [PDF]

, 2010
B. J. Reddy, Mallu Chenna Reddy
openalex   +1 more source