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573. The mechanism of hydrolysis of acid chlorides. Part X. Salt effects . R. F. Hudson, G. Moss
, J. Chem. Soc.
, 1964
, 2982
Asymmetric synthesis of enantiomerically enriched atropisomeric amides by desymmetrisation of N ,N -dialkylmesitamides . Jonathan Clayden, Paul Johnson, Jennifer H. Pink
, J. Chem. Soc., Perkin Trans. 1
, 2001
, 371
673. The mechanism of hydrolysis of acid chlorides. Part V. The effect of solvent and hydroxyl ions on the rate of solvolysis of substituted benzoyl chlorides . D. A. Brown, R. F. Hudson
, J. Chem. Soc.
, 1953
, 3352
Effective atherosclerotic plaque inflammation inhibition with targeted drug delivery by hyaluronan conjugated atorvastatin nanoparticles . Seyedmehdi Hossaini Nasr, Zahra Rashidijahanabad, Sherif Ramadan, Nate Kauffman, Narayanan Parameswaran, Kurt R. Zinn, Chunqi Qian, Ripla Arora, Dalen Agnew, Xuefei Huang
, Nanoscale
, 2020
, 12
, 9541
The reactivity of acyl chlorides towards sodium phosphaethynolate, Na(OCP): a mechanistic case study . Dominikus Heift, Zoltán Benkő, Riccardo Suter, René Verel, Hansjörg Grützmacher
, Chem. Sci.
, 2016
, 7
, 6125
The mechanism of Friedel–Crafts acylation . G. Baddeley, D. Voss
, J. Chem. Soc.
, 1954
, 418
Simple fluorene oxadiazole-based Ir(iii ) complexes with AIPE properties: synthesis, explosive detection and electroluminescence studies . Jia-Wei Liu, Ya-Nan Xu, Chun-Yan Qin, Zi-Ning Wang, Cong-Jin Wu, Yong-Hua Li, Shi Wang, Kenneth Yin Zhang, Wei Huang
, Dalton Trans.
, 2019
, 48
, 13305
112. Acylation reactions catalysed by strong acids. Part IV. “Benzoyl and substituted benzoyl perchlorates” as C -aroylating agents . H. Burton, P. F. G. Praill
, J. Chem. Soc.
, 1951
, 529
Notes . F. B. Deans, C. Eaborn, R. S. W. Braithwaite, P. F. Holt, H. R. Arthur, H. T. Cheung, E. R. A. Peeling, T. E. Peacock, D. E. Ames, T. F. Grey, E. M. Tanner, J. J. O'Donnell, Elizabeth Percival, R. A. Robinson, K. P. Ang, S. Bell, R. Foster, W. E. B. Soutar, D. I. Davies, D. H. Hey, C. W. Rees, F. C. Saunders
, J. Chem. Soc.
, 1959
, 2303
Three-dimensional fabrication of cell-laden biodegradable poly(ethylene glycol-co -depsipeptide) hydrogels by visible light stereolithography . Laura Elomaa, Chi-Chun Pan, Yaser Shanjani, Andrey Malkovskiy, Jukka V. Seppälä, Yunzhi Yang
, J. Mater. Chem. B
, 2015
, 3
, 8348