Inside front cover
文献信息
A graphical abstract is available for this content
期刊推荐
相关文献
Synthesis of platinum group metal nanoparticles assisted by CO2 reduction and H2 cogeneration at gas-diffusion electrodes
Guillermo Pozo, Luis Fernando Leon-Fernandez, Jan Fransaer, Xochitl Dominguez-Benetton
DOI: 10.1039/D3SU00046J
Univariate calibration by reversed regression of heteroscedastic data: a case study
Joel Tellinghuisen
DOI: 10.1039/B808667B
Degradation of herbicide atrazine in water by high voltage electrical discharge in comparison with Fenton oxidation and ultrasound treatments
Nadia Boussetta, Gérald Enderlin, Franck Merlier, Nabil Grimi
DOI: 10.1039/D3SU00103B
Substituting fossil-based with bio-based chemicals: the case of limonene as a greener pore expander for micellar templated silica
Ezzeldin Metwali, Santanu Maiti, Carola Schlumberger, Tadahiro Yokosawa, Benjamin Apeleo Zubiri, Erdmann Spiecker, Nicolas Vogel, Tobias Unruh, Matthias Thommes
DOI: 10.1039/D3SU00068K
Poly(vinyl acetate-co-crotonic acid) from bio-based crotonic acid: synthesis, characterization and carbon footprint evaluation
Alexandra Jorea, Adriano Parodi, Tiziana Benelli, Luca Ciacci, Maurizio Fagnoni, Paola Galletti, Laura Mazzocchetti, Davide Ravelli, Cristian Torri, Ivano Vassura, Chiara Samorì
DOI: 10.1039/D3SU00052D
A sustainable approach for the adsorption of methylene blue from an aqueous background: an adsorbent based on DES/CGS modified GO@ZrO2
Vishwajit Chavda, Brijesh Patel, Sneha Singh, Darshna Hirpara, V. Devi Rajeswari, Sanjeev Kumar
DOI: 10.1039/D3SU00236E
A microfluidic technique for monitoring bloodstream analytes indicative of C-peptide resistance in type 2 diabetes
Teresa D'Amico Oblak, Jennifer A. Meyer, Dana M. Spence
DOI: 10.1039/B816740K
Cu-catalysed Chan–Evans–Lam reaction meets deep eutectic solvents: efficient and selective C–N bond formation under aerobic conditions at room temperature‡
Luciana Cicco, Paola Vitale, Filippo Maria Perna, Joaquín García-Álvarez
DOI: 10.1039/D3SU00093A
Improving the activity of horseradish peroxidase in betaine-based natural deep eutectic systems
Liane Meneses, Nicolás F. Gajardo-Parra, Esteban Cea-Klapp, José Matías Garrido, Christoph Held, Ana Rita Duarte, Alexandre Paiva
DOI: 10.1039/D2SU00127F
您可能还喜欢
N-2,2-丙烯基-2-丙烯酰胺(CAS号:2555-13-7)通常如何合成?
N-2,2-丙烯基-2-丙烯酰胺通常通过丙烯酰胺与丙烯基卤化物的缩合反应合成。该反应通常在温和的条件下进行,使用适量的碱如吡啶作为催化剂。反应的选择性良好,产率...
什么是1,2-二碘四氟代乙烷(CAS号:354-65-4)?
1,2-二碘四氟代乙烷是一种有机化合物,化学式为C2F4I2,CAS号为354-65-4。它是一种无色透明液体,具有特殊的化学性质和物理性质,包括高沸点、低挥发...
3-溴-1H-吡咯[3,2-c]吡啶-4-碳腈(CAS号:1000341-71-8)适用哪些法规指南?
根据GHS(全球化学品统一分类和标签制度),3-溴-1H-吡咯[3,2-c]吡啶-4-碳腈被归类为第2类易燃液体。在欧盟,该化合物需要符合REACH法规的要求,...
1-氯甲基萘磺酸(CAS号:87491-79-0)安全吗?
1-氯甲基萘磺酸在使用时需要谨慎,因为它具有一定的刺激性和腐蚀性。操作时应佩戴适当的防护装备,如防化服、手套、护目镜等,避免直接接触皮肤和吸入其蒸汽。
二氯(二环戊二烯)铂(CAS号:12083-92-0)的主要用途是什么?
该化合物主要用于催化剂领域,特别是在有机合成中的催化氧化反应以及作为某些药物合成的中间体。此外,它还被研究用于纳米材料的制备。
3-溴-7-氯噻吩并[3,2-b]吡啶-6-甲腈(CAS号:798574-82-0)安全吗?
3-溴-7-氯噻吩并[3,2-b]吡啶-6-甲腈在处理时需要谨慎,因其含有溴和氯等强卤素,可能具有一定的刺激性和腐蚀性。使用时应佩戴适当的个人防护装备,避免皮肤...
(R)-1-((R)-2-(2’-二环己基膦苯基)三戊铁基]乙基(双-3,5-三氟甲基苯基)膦(CAS号:494227-32-6)的主要用途是什么?
该化合物主要用于有机合成领域,特别是作为催化剂或配体,在有机合成反应中发挥重要作用。此外,它还可能应用于催化加氢反应、偶联反应等。
3-[6-(Diphenylphosphoryl)-2-naphthyl]-1,10-phenanthroline(CAS号:1480371-38-7)安全吗?
3-[6-(Diphenylphosphoryl)-2-naphthyl]-1,10-phenanthroline在正常使用条件下相对安全,但在操作时应穿戴适当...
在合成中是否有ETHYL 2-(4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)CYCLOHEX-3-ENYL)ACETATE(CAS号:1166829-70-4)的替代品?
可以考虑使用类似结构的化合物作为替代品,如2-(4-环戊基环己烯基)乙酸酯,这种化合物在结构上相似,可能在某些合成路径中作为替代品。
如何处理含有3-(3-氨基丙基)丙酮缩甘油(CAS号:131606-42-3)的废料?
处理含有3-(3-氨基丙基)丙酮缩甘油的废料时,首先应确保遵守当地的环保法规。对于危险废物,应进行分类收集,然后送至专业的废物处理设施进行焚烧或安全填埋。在处理...
来源期刊
Analyst

Analyst publishes analytical and bioanalytical research that reports premier fundamental discoveries and inventions, and the applications of those discoveries, unconfined by traditional discipline barriers.













![(3R,4aR,7aS,9aR,10S,11R,13aR,13bS,15aS,15bR)-3,11-Dihydroxy-10-(hydroxymethyl)-4,4,7a,10,13a,15b-hexamethyl-1,2,3,4,4a,7,7a,8,9,9a,10,11,12,13,13a,13b,14,15,15a,15b-icosahydro-5H-naphtho[2',1':4,5]cyc
lohepta[1,2-a]naphthalen-5-one structure (3R,4aR,7aS,9aR,10S,11R,13aR,13bS,15aS,15bR)-3,11-Dihydroxy-10-(hydroxymethyl)-4,4,7a,10,13a,15b-hexamethyl-1,2,3,4,4a,7,7a,8,9,9a,10,11,12,13,13a,13b,14,15,15a,15b-icosahydro-5H-naphtho[2',1':4,5]cyc
lohepta[1,2-a]naphthalen-5-one structure](https://cnstatic.chemtradehub.com/structs/538/53800-21-8-9f18.webp)
