mi

Report on the inquiry into the management and use of Commonwealth environmental water : Inquiry into the management and use of Commonwealth environmental water / House of Representatives Standing Committee on the Environment and Energy

Australia. Parliament. House of Representatives. Standing Committee on the Environment and Energy, author, issuing body




mi

Murray-Darling basin plan : five-year assessment / Australian Government, Productivity Commission

Australia. Productivity Commission, author, issuing body




mi

Australia's drinking water : the coming crisis / John Archer

Archer, John, 1941-




mi

Palladium-catalyzed synthesis of [60]fullerene-fused furochromenones and further electrochemical functionalization

Org. Chem. Front., 2020, Advance Article
DOI: 10.1039/D0QO00264J, Research Article
Majid Hussain, Chuang Niu, Guan-Wu Wang
The palladium-catalyzed heteroannulation of [60]fullerene with 4-hydroxycoumarins affords [60]fullerene-fused furochromenones, which can be further derivatized via an electrochemical method to synthesize 1,2,3,4-adducts.
To cite this article before page numbers are assigned, use the DOI form of citation above.
The content of this RSS Feed (c) The Royal Society of Chemistry




mi

Expeditious access of chromone analogues via a Michael addition-driven multicomponent reaction

Org. Chem. Front., 2020, 7,987-992
DOI: 10.1039/D0QO00145G, Research Article
Jie Lei, Yong Li, Liu-Jun He, Ya-Fei Luo, Dian-Yong Tang, Wei Yan, Hui-Kuan Lin, Hong-yu Li, Zhong-Zhu Chen, Zhi-Gang Xu
A Michael addition-driven four-component reaction (4-CR) with four Ugi inputs was developed and utilized for the synthesis of chromone derivatives and tetrazole substituted chromones under mild reaction conditions.
The content of this RSS Feed (c) The Royal Society of Chemistry




mi

Copper-catalyzed tandem phosphorylative allenylation/cyclization of 1-(o-aminophenyl)prop-2-ynols with the P(O)–H species: access to C2-phosphorylmethylindoles

Org. Chem. Front., 2020, 7,980-986
DOI: 10.1039/D0QO00159G, Research Article
Xiao-Yan Liu, Yun-Xiang Zou, Hai-Liang Ni, Jing Zhang, Hong-Bo Dong, Long Chen
A novel method to synthesize C2-phosphorylmethylindoles via the carbocation formation initiated tandem phosphorylative allenylation/cyclization of 1-(o-aminophenyl)prop-2-ynols with the P(O)–H species has been developed.
The content of this RSS Feed (c) The Royal Society of Chemistry




mi

Palladium-catalyzed double carbonylation of propargyl amines and aryl halides to access 1-aroyl-3-aryl-1,5-dihydro-2H-pyrrol-2-ones

Org. Chem. Front., 2020, 7,1006-1010
DOI: 10.1039/D0QO00007H, Research Article
Jun Ying, Zhengjie Le, Zhi-Peng Bao, Xiao-Feng Wu
A palladium-catalyzed carbonylative procedure for the synthesis of 1-aroyl-3-aryl-1,5-dihydro-2H-pyrrol-2-ones from propargyl amines and aryl halides with TFBen as the CO source has been developed.
The content of this RSS Feed (c) The Royal Society of Chemistry




mi

Rh-Catalyzed nitrene alkyne metathesis/formal C–N bond insertion cascade: synthesis of 3-iminoindolines

Org. Chem. Front., 2020, Advance Article
DOI: 10.1039/D0QO00294A, Research Article
Kemiao Hong, Su Zhou, Wenhao Hu, Xinfang Xu
A Rh-catalyzed nitrene/alkyne metathesis (NAM) cascade reaction terminated by a formal C–N bond insertion has been developed, which provides facile access to the tricyclic 3-iminoindolines in good yields with broad substrate scope.
To cite this article before page numbers are assigned, use the DOI form of citation above.
The content of this RSS Feed (c) The Royal Society of Chemistry




mi

Examining the vinyl moiety as a protecting group for hydroxyl (–OH) functionality under basic conditions

Org. Chem. Front., 2020, Advance Article
DOI: 10.1039/D0QO00202J, Research Article
Vladimir V. Voronin, Maria S. Ledovskaya, Konstantin S. Rodygin, Valentine P. Ananikov
A method for the protection and deprotection of alcohols via vinylation and devinylation reactions is proposed. Stability of the vinyl protecting group under various conditions is studied and synthetic applicability is demonstrated.
To cite this article before page numbers are assigned, use the DOI form of citation above.
The content of this RSS Feed (c) The Royal Society of Chemistry




mi

Access to SCN-containing thiazolines via electrochemical regioselective thiocyanothiocyclization of N-allylthioamides

Org. Chem. Front., 2020, Advance Article
DOI: 10.1039/D0QO00300J, Research Article
Yan-An Zhang, Zhong Ding, Peng Liu, Wei-Si Guo, Li-Rong Wen, Ming Li
An electrochemical thiocyclization of N-allylthioamides has been developed for the synthesis of SCN-containing 2-thiazolines and NCS-containing thiazines.
To cite this article before page numbers are assigned, use the DOI form of citation above.
The content of this RSS Feed (c) The Royal Society of Chemistry




mi

Direct organocatalytic asymmetric Michael reaction of fluorine hemiaminal-type nucleophile to 4-nitro-5-styrylisoxazoles

Org. Chem. Front., 2020, Advance Article
DOI: 10.1039/D0QO00348D, Research Article
Luyao Li, Bo Zhu, Huihui Fan, Zhiyong Jiang, Junbiao Chang
Herein, we report a chiral bifunctional thiourea catalyzed asymmetric Michael addition reaction between 2-(trifluoromethyl)oxazol-5(2H)-one as a direct C-2-position nucleophile to 4-nitro-5-styrylisoxazoles for the first time.
To cite this article before page numbers are assigned, use the DOI form of citation above.
The content of this RSS Feed (c) The Royal Society of Chemistry




mi

Turn-on fluorescence sensors based on dynamic intramolecular N→B-coordination

Org. Chem. Front., 2020, Advance Article
DOI: 10.1039/D0QO00267D, Research Article
Raphael Koch, Yu Sun, Andreas Orthaber, Antonio J. Pierik, Frank Pammer
A series of ten aryl-triazole-functionalized boranes bearing BMes2-groups and capable of forming intramolecular five-membered N→B-coordinated heterocycles, has been prepared by 1,3-dipolar cycloaddition.
To cite this article before page numbers are assigned, use the DOI form of citation above.
The content of this RSS Feed (c) The Royal Society of Chemistry




mi

Hyperforones A–C, benzoyl-migrated [5.3.1]-type polycyclic polyprenylated acylphloroglucinols from Hypericum forrestii

Org. Chem. Front., 2020, 7,1070-1076
DOI: 10.1039/D0QO00152J, Research Article
Wei-Jia Lu, Wen-Jun Xu, Yan-Qiu Zhang, Yi-Ran Li, Xin Zhou, Qi-Ji Li, Hao Zhang, Jun Luo, Ling-Yi Kong
Unprecedented benzoyl-migrated polycyclic polyprenylated acylphloroglucinols with a unique C-1 H-substituted bicyclo[5.3.1]hendecane framework, hyperforones A–C (1–3), were isolated from Hypericum forrestii.
The content of this RSS Feed (c) The Royal Society of Chemistry




mi

Discrete boronate ester ladders from the dynamic covalent self-assembly of oligo(phenylene ethynylene) derivatives and phenylenebis(boronic acid)

Org. Chem. Front., 2020, 7,1082-1094
DOI: 10.1039/D0QO00083C, Research Article
Vasileios Drogkaris, Brian H. Northrop
Reversible boronate ester chemistry enables the controlled, dynamic self-assembly of olig(phenylene ethynylene)s into highly conjugated ladder frameworks.
The content of this RSS Feed (c) The Royal Society of Chemistry




mi

Differential formation of nitrogen-centered radicals leading to unprecedented, regioselective bromination of N,N'-(1,2-phenylene)bisamides and 2-amidophenols

Org. Chem. Front., 2020, 7,1095-1106
DOI: 10.1039/C9QO01508F, Research Article
Damoder Reddy Motati, Dilipkumar Uredi, Amarender Goud Burra, J. Phillip Bowen, Frank R. Fronczek, Clint R. Smith, E. Blake Watkins
A highly efficient, site-selective, visible light-accelerated, remote C–H halogenation of unsymmetrical aromatic bisamides/amidoesters has been developed.
The content of this RSS Feed (c) The Royal Society of Chemistry




mi

Toward C2-nitrogenated chromones by copper-catalyzed β-C(sp2)–H N-heteroarylation of enaminones

Org. Chem. Front., 2020, 7,1107-1112
DOI: 10.1039/D0QO00065E, Research Article
Tian Luo, Jie-Ping Wan, Yunyun Liu
The synthesis of C2-nitrogenated chromones has been performed via reactions of enaminones and nitrogen nucleophiles based on an unconventional β-C–H bond functionalization and a featured chromone annulation of enaminones.
The content of this RSS Feed (c) The Royal Society of Chemistry




mi

An Aspidosperma-type alkaloid dimer from Tabernaemontana bovina as a candidate for the inhibition of microglial activation

Org. Chem. Front., 2020, Advance Article
DOI: 10.1039/D0QO00296H, Research Article
Yang Yu, Si-Meng Zhao, Mei-Fen Bao, Xiang-Hai Cai
As a representative of twelve undescribed Aspidosperma-type alkaloid dimers, tabernaemontine F (6) inhibited microglial activation by blocking P38 MAPK activation, revealing a potential candidate for chronic neurodegenerative diseases.
To cite this article before page numbers are assigned, use the DOI form of citation above.
The content of this RSS Feed (c) The Royal Society of Chemistry




mi

Mechanism and Origins of Stereo- and Enantioselectivities of Palladium-Catalyzed Hydroamination of Racemic Internal Allenes via Dynamic Kinetic Resolution: A Computational Study

Org. Chem. Front., 2020, Accepted Manuscript
DOI: 10.1039/D0QO00174K, Research Article
Zhenzhen Wu, Mei Zhang, Yu Shi, Genping Huang
Density functional theory calculations have been performed to investigate the Pd-catalyzed hydroamination of racemic internal allenes with pyrazoles. The computations show that the originally proposed reaction mechanisms initiated by the...
The content of this RSS Feed (c) The Royal Society of Chemistry




mi

A Vinylogous Michael Reaction of 2-Furanones Dimers to α, β-Unsaturated Nitroolefins for Constructing Chiral γ, γ-Disubstituted Butenolides

Org. Chem. Front., 2020, Accepted Manuscript
DOI: 10.1039/D0QO00376J, Research Article
Zhushuang Bai, Cairong Zhang, Yongyi Chen, Aiqin Liu, Xinyu Wang, Chuna Yan, Xuechao Liu, Xiaoru Zhang, Ying Li, Ye Yuan, Zemei Ge, Jingxiang Pang, Yongshuai Chai, Xin Wang, Runtao Li
An efficient bifunctional thiourea catalyzed asymmetric vinylogous Michael addition of 2-furanones dimers to α, β-unsaturated nitroolefins has been developed to give the functional chiral γ,γ-disubstituted butenolides in good yields (up...
The content of this RSS Feed (c) The Royal Society of Chemistry




mi

Rhodium(III)-catalyzed synthesis of 3-trifluoromethylindanones from N-Methoxybenzamides via C-H activation and Claisen/Retro-Claisen reaction

Org. Chem. Front., 2020, Accepted Manuscript
DOI: 10.1039/D0QO00330A, Research Article
Satyasheel Sharma, Bharatkumar Chaudhary, Neeraj Kulkarni
The Rhodium(III)-catalyzed reaction of N-methoxybenzamides as a directing group with β-trifluoromethyl-α,β-unsaturated ketones is reported. The reaction involved sp2 C−H activation, followed by Claisen condensation involving C-N bond cleavage to form...
The content of this RSS Feed (c) The Royal Society of Chemistry




mi

Handbook for Chemical Society authors / [Chemical Society]

Chemical Society (Great Britain)




mi

The art of scientific writing : from student reports to professional publications in chemistry and related fields / Hans F. Ebel, Claus Bliefert, William E. Russey

Ebel, Hans Friedrich




mi

The chemist's English / Robert Schoenfeld

Schoenfeld, Robert




mi

Writing and presenting scientific papers / Birgitta Malmfors, Phil Garnsworthy, Michael Grossman

Malmfors, Birgitta




mi

Handbook of microscopy for nanotechnology / edited by Nan Yao, Zhong Lin Wang




mi

Nanoelectromechanics in engineering and biology / Michael Pycraft Hughes

Hughes, Michael Pycraft, 1970-




mi

Introduction to nanoscale science and technology / edited by Massimiliano Di Ventra, Stephane Evoy. James R. Heflin




mi

Noncontact atomic force microscopy / S. Morita, R. Wiesendanger, E. Meyer (eds.)




mi

Micromachines as tools for nanotechnology / H. Fujita, [editor]




mi

Magnetic microscopy of nanostructures / H. Hopster, H.P. Oepen (eds.)




mi

Nanotechnology : basic science and emerging technologies / Mick Wilson ... [et al.]




mi

Nano-engineering in science and technology : an introduction to the world of nano-design / Michael Rieth

Rieth, Michael




mi

Nanoscale calibration standards and methods : dimensional and related measurements in the micro- and nanometer range / edited by Günter Wilkening, Ludger Koenders




mi

Nanochemistry : a chemical approach to nanomaterials / Geoffrey A. Ozin and André C. Arsenault

Ozin, Geoffrey A., 1943-




mi

Handbook of semiconductor nanostructures and nanodevices / edited by Alexander A. Balandin, Kang L. Wang




mi

Nanostructures : novel architecture / Mircea V. Diudea, editor




mi

Micromanufacturing and nanotechnology / N.P. Mahalik (ed.)




mi

Nanochemistry / G.B. Sergeev

Sergeev, G. B. (Gleb Borisovich)




mi

Nanotechnology / G. Schmid ... [et al.] (eds.)




mi

Nanotechnology for biology and medicine : at the building block level / Gabriel A. Silva, Vladimir Parpura, editors




mi

Nanoscale physics for materials science / Takaaki Tsurumi ... [et al.]




mi

Chemistry of nanocarbons / edited by Takeshi Akasaka, Fred Wudl, Shigeru Nagase




mi

Nanotechnology for a sustainable world : global artificial photosynthesis as nanotechnology's moral culmination / T. Faunce

Faunce, T




mi

Nanotechnology research directions for societal needs in 2020 : retrospective and outlook / Mihail C. Roco, Chad A. Mirkin, Mark C. Hersam

Roco, M.C. (Mihail C.)




mi

Microfabrication for industrial applications / Regina Luttge

Luttge, Regina




mi

Chemistry and physics of modern materials : processing, production and applications / edited by Jimsher N. Aneli, DSc, Alfonso Jiménez, PhD, and Stefan Kubica, PhD




mi

Micro and nano fabrication : tools and processes / Hans H. Gatzen, Volker Saile, Jürg Leuthold ; with a foreword and an introduction by Richard S. Muller

Gatzen, Hans-Heinrich, author




mi

Nanotechnology : the future is tiny / Michael Berger (Nanowerk LLC, Berlin, Germany)

Berger, Michael, author




mi

Nanoscience : the science of the small in physics, engineering, chemistry, biology and medicine / Hans-Eckhardt Schaefer

Schaefer, Hans-Eckhardt, author




mi

Biogenic production of gold and silver nanoparticles using extracts from indigenous Australian plants : their synthesis, optimisation, characterisation and antibacterial activities / Monali Shah

Shah, Monali, author