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Theatre and social media / Patrick Lonergan

Lonergan, Patrick




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Learning to teach drama 11-18 / Andy Kempe and Helen Nicholson

Kempe, Andy




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Masterclass in drama education : transforming teaching and learning / Michael Anderson

Anderson, Michael, 1969-




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Not just a mirror : looking for the political theatre of today / edited by Florian Malzacher ; a publication by House on Fire ; translations, Daria Kassovsky [and 3 others]




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Theatre & the rural / Jo Robinson ; [foreword by Mike Pearson]

Robinson, Jo (Professor), author




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Politics, ethics and performance : Hélène Cixous and the Théâtre du Soleil / Hélène Cixous ; edited by Lara Stevens

Cixous, Hélène, 1937- author




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Modern popular theatre / Jason Price

Price, Jason, author




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Performance and participation : practices, audiences, politics / edited by Anna Harpin & Helen Nicholson




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Theatre and phenomenology : manual philosophy / Daniel Johnston

Johnston, Daniel, author




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Chorus song of the indri (Indri indri: Primates, Lemuridae): Group differences and analysis of within-group vocal interactions

Chorus song of the indri (Indri indri: Primates, Lemuridae): Group differences and analysis of within-group vocal interactions Baker-Medard, Merrill S. A.; Baker, Myron C.; Logue, David M. The loud chorus songs of the group-living lemur Indri indri are a striking feature of rainforest areas of eastern Madagascar. Despite some research on the conspicuous vocal display of the indri, two hypotheses have not been addressed: do groups differ in the acoustic properties of their songs, and is there evidence of coordinated singing between individuals within groups. We recorded and analyzed the songs of three indri groups to examine these two questions. To answer the first question, we made quantitative spectral measures on songs of the three groups and performed multivariate analyses of the acoustic features of the notes constituting the songs. Our results showed songs of the three groups differed significantly, although there was overlap between groups. To answer the second question, we classified note types and quantified their occurrence as overlapping and abutting pairs. We found non-random associations between sequential note types in all three indri groups. These associations were consistent among groups, suggesting that individuals follow consistent answering rules when contributing to choruses. Whether indris use acoustic group identifiers in management of behavioral strategies and how within-group coordinated note production might function remain unknown. We compare our results to a number of taxonomically diverse species that live in groups and broadcast chorus and duet vocal signals. Open access article. Creative Commons Attribution 4.0 International License (CC BY 4.0) applies.




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Working From Home For The First Time in 3 Years – Expect Some Writing/Open Source From Me

Like many of you I’m working from home for a while. As a mental health strategy, I’m going to do some writing and coding in the hour or so I get back each day from not having to commute. The first post, which will follow today, will be my thoughts on working from home. I […]




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Indian Railways converts coaches into isolation wards for virus patients

Network to provide 80,000 mobile beds after national lockdown shuts passenger services   




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India to relax some lockdown restrictions

Limited manufacturing and agricultural work to resume after April 20




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Learning bio-micro-nanotechnology / Mel I. Mendelson

Hayden Library - TP248.25.N35 M46 2013




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Perspectivas sobre el desarrollo de las nanotecnologías en América Latina / Guillermo Foladori, Noela Invernizzi, Edgar Záyago Lau, coordinadores

Hayden Library - T174.7.P46 2012




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Advanced in nanoscience and technology: selected, peer reviewed papers from the 10th China International Nanoscience and Technology Symposium, Hangzhou (2011) and the Nano-Products Exposition, sponsored by Chinese Society of Micro-NanoTechnology and IEEE

Hayden Library - T174.7.C459 2011




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Solution synthesis of inorganic films and nanostructured materials: symposium held April 9-13, 2012, San Francisco, California, U.S.A. / editors, Menka Jain ... [et al.]

Hayden Library - TA418.9.N35 S967 2012




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Solution synthesis of inorganic functional materials -- films, nanoparticles and nanocomposites: symposium held April 1-5, 2013, San Francisco, California, U.S.A. / editors, Menka Jain, Quanxi Jia, Teresa Puig, Hiromitsu Kozuba

Hayden Library - TA418.9.N35 S656 2013




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Nanoimaging and nanospectroscopy: 27-29 August 2013, San Diego, California, United States / Prabhat Verma, Alexander Egner, editors ; sponsored and published by SPIE

Online Resource




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Advanced fabrication technologies for micro/nano optics and photonics VII: 3-5 February 2014, San Francisco, California, United States / Georg von Freymann, Winston V. Schoenfeld, Raymond C. Rumpf, editors ; sponsored by SPIE ; cosponsored by Samsung Adva

Online Resource




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Foundations of nanotechnology. Sabu Thomas, Saeedeh Rafiei, Shima Maghsoodlou

Online Resource




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Frontiers in micro-nano science and technology: selected, peer reviewed papers from the 12th China International Nanoscience and Technology Symposium, Chengdu (2013) and the Nano-Products Exposition, sponsored by Chinese Society of Micro-Nano Technology,

Hayden Library - T174.7.C456 2013




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Micro-nano technology XV: selected, peer reviewed papers from the 15th Annual Conference and 4th International Conference of the Chinese Society of Micro-Nano Technology (CSMNT 2013), November 3-6, 2013, Tianjin, China / edited by Fei Tang ; [Zheng You, c

Hayden Library - T174.7.C46 2013




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Emerging nanotechnologies for manufacturing / edited by Waqar Ahmed, Mark Jackson

Barker Library - T174.7.A364 2014




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Nanoimaging and nanospectroscopy II: 17-19 August 2014, San Diego, California, United States / Prabhat Verma, Alexander Egner, editors ; sponsored and published by SPIE

Online Resource




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Proceedings of the 13th International Conference of the European Society for Precision Engineering and Nanotechnology: May 27th-31st, 2013, Berlin, Germany / editors, R. Leach, P. Shore ; proceedings compilation, T. Horwood, D. Nyman, D. Phillips, N. Will

Barker Library - T174.7.I59 2013




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Proceedings of the 14th International Conference of the European Society for Precision Engineering and Nanotechnology: June 2nd-6th, 2014, Dubrovnik, Croatia / editors, R. Leach ; proceedings compilation, N. Charlton, D. Nyman, D. Phillips

Barker Library - T174.7.I59 2014




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NANOFORUM 2013: Rome, Italy, 18-20 September 2013 / editors, Marco Rossi, Carlo Mariani, Maria Letizia Terranova ; sponsoring organizations, Sapienza University of Rome, in collaboration with Sapienza Nanotechnology and Nanoscience Laboratory [and 4 other

Online Resource




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Nanoscale materials and devices for electronics, photonics and solar energy / Anatoli Korkin, Stephen Goodnick, Robert Nemanich, editors

Online Resource




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CRC concise encyclopedia of nanotechnology / edited by Boris Ildusovich Kharisov, Oxana Vasilievna Kharissova, and Ubaldo Ortiz-Mendez

Online Resource




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Nano meets macro: social perspectives on nanoscale sciences and technologies / editors, Kamilla Lein Kjølberg, Fern Wickson

Online Resource




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Quaternary ecology, evolution and biogeography [electronic resource] / Valentí Rull.

London : Academic Press, 2020.




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School closures and the online preparedness of children during the COVID-19 pandemic [electronic resource] / by Marc Frenette, Kristyn Frank, and Zechuan Deng

[Ottawa] : Statistics Canada = Statistique Canada, 2020




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COVID-19 pandemic [electronic resource]: school closures and the online preparedness of children / by Marc Frenette, Kristyn Frank and Zechuan Deng

[Ottawa] : Statistics Canada = Statistique Canada, 2020




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Canadians report lower self-perceived mental health during the COVID-19 pandemic [electronic resource] / by Leanne Findlay and Rubab Arim

[Ottawa] : Statistics Canada = Statistique Canada, 2020




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Highly Z-selective synthesis of 1,3-oxathiol-2-ylidenes and 4-methylene-oxazolidine-2-thiones via atom-specific 5-exo-dig cyclization of propargyl alcohol with isothiocyanate

Org. Biomol. Chem., 2020, Advance Article
DOI: 10.1039/D0OB00083C, Paper
S. Antony Savarimuthu, D. G. Leo Prakash, S. Augustine Thomas, Thirumanavelan Gandhi, Mrinal K. Bera
The Z-selectivity observed in imine and alkene motifs after 5-exo-dig cyclization of propargyl alcohol and isothiocyanate is rare in the literature and this selectivity can be attributed to electronic and steric factors of the imine and alkene motif respectively.
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




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A modular approach to the bisbenzylisoquinoline alkaloids tetrandrine and isotetrandrine

Org. Biomol. Chem., 2020, 18,3047-3068
DOI: 10.1039/D0OB00078G, Paper
Ramona Schütz, Maximilian Meixner, Iris Antes, Franz Bracher
A modular short-step synthesis of the bisbenzylisoquinoline alkaloids tetrandrine and isotetrandrine was developed employing N-acyl-Pictet–Spengler reaction and Ullman diaryl ether synthesis as central steps.
The content of this RSS Feed (c) The Royal Society of Chemistry




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Catalyst and solvent switched divergent C–H functionalization: oxidative annulation of N-aryl substituted quinazolin-4-amine with alkynes

Org. Biomol. Chem., 2020, 18,3032-3037
DOI: 10.1039/D0OB00318B, Communication
Siddi Ramulu Meesa, Praveen Kumar Naikawadi, Kishan Gugulothu, K. Shiva Kumar
Catalyst and solvent controlled ortho/peri site-selective oxidative annulation of C–H bonds of N-aryl substituted quinazolin-4-amines with internal alkynes.
The content of this RSS Feed (c) The Royal Society of Chemistry




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Non-biaryl atropisomerism at the C–B bond in sterically hindered aminoarylboranes

Org. Biomol. Chem., 2020, 18,3007-3011
DOI: 10.1039/D0OB00421A, Communication
Mélodie Birepinte, Frédéric Robert, Sandra Pinet, Laurent Chabaud, Mathieu Pucheault
Sterically hindered aminoarylboranes with atropisomerism about the C–B bond were prepared and resolved by chiral stationary phase HPLC.
The content of this RSS Feed (c) The Royal Society of Chemistry




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Asymmetric synthesis of (−)-solanidine and (−)-tomatidenol

Org. Biomol. Chem., 2020, 18,3169-3176
DOI: 10.1039/D0OB00457J, Paper
Yun Wang, Guanxin Huang, Yong Shi, Wei-sheng Tian, Chunlin Zhuang, Fen-Er Chen
The asymmetric synthesis of (−)-solanidine (1) and (−)-tomatidenol (2) has been achieved by employing a cascade ringswitching reaction and a cascade azide reduction/intramolecular reductive amination with 32% and 18.7% overall yields respectively.
The content of this RSS Feed (c) The Royal Society of Chemistry




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Experimental results and computational insight into sequential reactions of β-(2-aminophenyl)-α,β-ynones with aryl isocyanates/benzoyl isothiocyanate

Org. Biomol. Chem., 2020, 18,3177-3189
DOI: 10.1039/D0OB00087F, Paper
Antonio Arcadi, Massimiliano Aschi, Marco Chiarini, Fabio Marinelli, Vincenzo Marsicano, Gustavo Portalone
The selective formation of quinazoline vs. benzoxazine  and benzothiazine derivatives from β-(2-aminophenyl)-α,β-ynones and aryl isocyanates/benzoyl isothiocyanate was explored. DFT calculations provide a plausible rationale.
The content of this RSS Feed (c) The Royal Society of Chemistry




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Half-sandwich (η5-Cp*)Rh(III) complexes of pyrazolated organo-sulfur/selenium/tellurium ligands: efficient catalysts for base/solvent free C–N coupling of chloroarenes under aerobic conditions

Org. Biomol. Chem., 2020, Advance Article
DOI: 10.1039/D0OB00538J, Paper
Charu Sharma, Avinash Kumar Srivastava, Kamal Nayan Sharma, Raj Kumar Joshi
Three new Rh(III) complexes of organochalcogen (S/Se/Te) ligands were synthesized and along with a co-catalyst Cu(OAc)2, used for the base/solvent free catalysis of Buchwald type C–N coupling of amines and aryl chlorides under aerobic conditions.
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




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Photocatalytic xanthate-based radical addition/cyclization reaction sequence toward 2-biphenyl isocyanides: synthesis of 6-alkylated phenanthridines

Org. Biomol. Chem., 2020, Advance Article
DOI: 10.1039/D0OB00136H, Communication
Pedro López-Mendoza, Luis D. Miranda
A photocatalytic xanthate-based radical addition/cyclization reaction cascade toward 2-biphenylisocyanides is described as a practical and modular approach to 6-alkylated phenanthridines.
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




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N-Hydroxy peptides: solid-phase synthesis and β-sheet propensity

Org. Biomol. Chem., 2020, Advance Article
DOI: 10.1039/D0OB00664E, Paper
Matthew P. Sarnowski, Juan R. Del Valle
Backbone amide hydroxylation of peptide strands enhances β-hairpin folding.
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




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Ni(II)-Catalyzed vinylic C–H functionalization of 2-acetamido-3-arylacrylates to access isotetronic acids

Org. Biomol. Chem., 2020, Advance Article
DOI: 10.1039/D0OB00557F, Paper
Biswajit Roy, Eshani Das, Avijit Roy, Dipakranjan Mal
A ligand-free Ni(II)-catalyzed cascade annulation reaction for the synthesis of 4-aryl-substituted isotetronic acids from 2-acetamido-3-arylacrylates via vinylic C–H functionalization is reported.
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




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Catalyst- and Solvent-Free Efficient Access to N-Alkylated Amines via Reductive Amination using HBPin

Org. Biomol. Chem., 2020, Accepted Manuscript
DOI: 10.1039/D0OB00740D, Communication
ARNAB RIT, Vipin Kumar Pandey, Somnath Bauri
A sustainable approach which works under catalyst- and solvent-free conditions for the synthesis of structurally diverse secondary amines has been uncovered. This one-pot protocol works efficiently at room temperature and...
The content of this RSS Feed (c) The Royal Society of Chemistry




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Electrochemically enabled functionalization of indoles or anilines to synthesis of hexafluoroisopropoxy indole and anilinederivatives

Org. Biomol. Chem., 2020, Accepted Manuscript
DOI: 10.1039/D0OB00157K, Communication
Zu-yu Mo, Xin-Yu Wang, Yu-zhen Zhang, Li Yang, Hai-Tao Tang, Ying-Ming Pan
An environmentally benign electrochemically enabled site-selective functionalization of indole or aniline derivatives with hexafluoroisopropanol in the presence of tetrabutyl ammonium hexafluorophosphate as redox catalyst and electrolyte was demonstrated in this...
The content of this RSS Feed (c) The Royal Society of Chemistry




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Enantioselective Synthesis of Indanone Spiro-Isochromanone Derivatives via Dinuclear Zinc-Catalyzed Michael/Transesterification Tandem Reaction

Org. Biomol. Chem., 2020, Accepted Manuscript
DOI: 10.1039/D0OB00541J, Paper
Xiao-Chao Yang, Meng Xu, Jin-Bao Wang, Meng-Meng Liu, Francois Mathey, Yuan-Zhao Hua, Mincan Wang
An enantioselective Michael/transesterification tandem reaction of α-hydroxy indanones with ortho-ester chalcones was realized by dinuclear zinc catalysts. A series of enantiomerically pure spiro[indanone-2,3’-isochromane-1-one] derivatives were obtained in good yields with...
The content of this RSS Feed (c) The Royal Society of Chemistry




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Protein labeling approach to improve lysosomal targeting and efficacy of antibody–drug conjugates

Org. Biomol. Chem., 2020, 18,3229-3233
DOI: 10.1039/D0OB00265H, Communication
Ying Han, Yifan Da, Mingjia Yu, Yaping Cheng, Xin Wang, Jiale Xiong, Guoying Guo, Yan Li, Xianxing Jiang, Xiaoqing Cai
An anti-EGFR nanobody was labeled at the C-terminus with a lysosome-sorting NPGY (Asn-Pro-Gly-Tyr) motif via sortase-mediated ligation to enhance the clathrin-mediated endocytosis.
The content of this RSS Feed (c) The Royal Society of Chemistry




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O-Cyclopropyl hydroxylamines: gram-scale synthesis and utility as precursors for N-heterocycles

Org. Biomol. Chem., 2020, 18,3281-3287
DOI: 10.1039/D0OB00611D, Paper
Kaitlyn Lovato, Urmibhusan Bhakta, Yi Pin Ng, László Kürti
A novel and scalable synthesis of O-cyclopropyl hydroxylamines is reported. These compounds are bench-stable and have been shown to be practical precursors for the synthesis of N-heterocycles via a di-heteroatom [3,3]-sigmatropic rearrangement.
The content of this RSS Feed (c) The Royal Society of Chemistry