Catalyst-free facile synthesis of 2-substituted benzothiazoles
文献情報
Siva S. Panda, Alexander A. Oliferenko
2-Substituted benzothiazoles were synthesized in excellent yields by a benzotriazole methodology, with the conditions being efficient, green, economical, and suitable for broad applications in medicinal chemistry and the synthesis of specialty chemicals.
関連文献
Understanding dissolution process of chitin crystal in ionic liquids: theoretical study
Takuya Uto, Satoshi Idenoue, Kazuya Yamamoto, Jun-ichi Kadokawa
DOI: 10.1039/C8CP02749H
An ab initio study of sensing applications of MoB2 monolayer: a potential gas sensor
Amreen Bano, Jyoti Krishna, Devendra K. Pandey, N. K. Gaur
DOI: 10.1039/C8CP07038E
Infrared spectroscopic characterization of phosphate binding at the goethite–water interface
Stella Gypser, Peter Leinweber, Dirk Freese
DOI: 10.1039/C8CP07168C
The role of solvation models on the computed absorption and emission spectra: the case of fireflies oxyluciferin
Cristina García-Iriepa, Madjid Zemmouche, Isabelle Navizet
DOI: 10.1039/C8CP07352J
Dynamic micellar oligomers of amyloid beta peptides play a crucial role in their aggregation mechanisms
Bertrand Morel, Maria Paz Carrasco, Samuel Jurado, Carmen Marco, Francisco Conejero-Lara
DOI: 10.1039/C8CP02685H
Nature of halogen bonding involving π-systems, nitroxide radicals and carbenes: a highlight of the importance of charge transfer
Adrian M. Mak
DOI: 10.1039/C8CP04075C
Globule–stretch transition of a self-attracting chain in the repulsive active particle bath
Yi-qi Xia, Wen-de Tian
DOI: 10.1039/C8CP05976D
Gold substrates of controlled roughness and electrokinetic properties formed by nanoparticle deposition
Maria Morga, Małgorzata Nattich-Rak, Magdalena Oćwieja, Zbigniew Adamczyk
DOI: 10.1039/C9CP00440H
The energy level of the Fe2+/3+-transition in BaTiO3 and SrTiO3 single crystals
Issei Suzuki, Leonard Gura, Andreas Klein
DOI: 10.1039/C8CP07872F
Temperature-dependent crystalline structure and phase transition of poly(butylene adipate) end-functionalized by multiple hydrogen-bonding groups
Jianna Bao, Huabo Fan, Xiaojia Xue, Qing Xie, Pengju Pan
DOI: 10.1039/C8CP05066J
こちらもおすすめ
2-ブロモ-9,9-ジフェニル-9H-フルオレンの主な用途は何ですか?
2-溴-9,9-二苯基芴は、医薬品、工業材料、有機合成の研究分野で応用されます。特に、レーザー材料や機能性ポリマーの合成に使用されることがあります。また、蛍光色...
四氯化铱の市場動向や研究トレンドはどうですか?
四氯化铱の市場は研究開発分野で注目されており、特にナノ技術や金属有機框架(MOFs)の分野での需要が増加傾向にあります。価格は安定しており、中国や韓国での生産が...
1-(4-溴-3-氟苯基)-2-氯乙酮を含む廃棄物はどのように処理すべきですか?
1-(4-溴-3-氟苯基)-2-氯乙酮 (CAS番号: 1260857-14-4) の廃棄物は専門的な廃棄処理が必要です。まず、廃棄物は密閉された容器に収集し、...
苦参酚Kとは何ですか?
苦参酚Kは、CAS番号101236-49-1を持つ化合物で、主に天然由来の生薬から抽出されます。この化合物は、抗炎症作用や抗癌作用を持つことが報告されています。
POTASSIUM (1-(TERTBUTOXYCARBONYL)AZETIDIN-3-YL)TRIFLUOROBORATE を含む廃棄物はどのように処理すべきですか?
POTASSIUM (1-(TERTBUTOXYCARBONYL)AZETIDIN-3-YL)TRIFLUOROBORATE を含む廃棄物は、まず安全なエント...
4-庚基-4’-联苯羧酸の市場動向や研究トレンドはどうですか?
4-庚基-4’-聯苯羧酸は、特殊化学品や合成化学の分野で用いられる化学物質ですが、市場動向としては、研究開発の進展とともに需要が増加しています。また、環境配慮型...
6-ブロモ-3-メトキシ-1-フェニル-1H-インドゾールを含む廃棄物はどのように処理すべきですか?
6-ブロモ-3-メトキシ-1-フェニル-1H-インドゾールを含む廃棄物は、適切な化学廃棄処理が必要です。通常、廃棄物は密閉容器に収集され、専門の廃棄処理業者に引...
4,4-二甲基-2-吡咯烷酮はどの業界で使用されていますか?
4,4-二甲基-2-吡咯烷酮は医薬、ポリマー、センサー、半導体などの業界で広く使用されています。特に溶媒としての性能が高く評価されています。
掲載誌
Green Chemistry

Green Chemistry provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on, but not limited to, the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998). Green chemistry is the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry is at the frontiers of this continuously-evolving interdisciplinary science and publishes research that attempts to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. Submissions on all aspects of research relating to the endeavour are welcome. The journal publishes original and significant cutting-edge research that is likely to be of wide general appeal. To be published, work must present a significant advance in green chemistry. Papers must contain a comparison with existing methods and demonstrate advantages over those methods before publication can be considered. For more information please see this Editorial. Coverage includes the following, but is not limited to: Design (e.g. biomimicry, design for degradation/recycling/reduced toxicity…) Reagents & Feedstocks (e.g. renewables, CO2, solvents, auxiliary agents, waste utilization…) Synthesis (e.g. organic, inorganic, synthetic biology…) Catalysis (e.g. homogeneous, heterogeneous, enzyme, whole cell…) Process (e.g. process design, intensification, separations, recycling, efficiency…) Energy (e.g. renewable energy, fuels, photovoltaics, fuel cells, energy storage, energy carriers…) Applications (e.g. electronics, dyes, consumer products, coatings, pharmaceuticals, preservatives, building materials, chemicals for industry/agriculture/mining…) Impact (e.g. safety, metrics, LCA, sustainability, (eco)toxicology…) Green chemistry is, by definition, a continuously-evolving frontier. Therefore, the inclusion of a particular material or technology does not, of itself, guarantee that a paper is suitable for the journal. To be suitable, the novel advance should have the potential for reduced environmental impact relative to the state of the art. Green Chemistry does not normally deal with research associated with 'end-of-pipe' or remediation issues.











![5-Methyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazin-2-amine structure 5-Methyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazin-2-amine structure](https://static.chemtradehub.com/structs/122/1227210-33-4-8d64.webp)


