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Accounts of Chemical Research
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April 15, 2015
Sm(II)-Mediated Electron Transfer to Carboxylic Acid Derivatives: Development of Complexity-Generating Cascades
Xavier Just-Baringo, David J Procter
Angewandte Chemie (International Ed. in English)
|
July 14, 2016
C-H Coupling Reactions Directed by Sulfoxides: Teaching an Old Functional Group New Tricks
Alexander P Pulis, David J Procter
Anaesthesia
|
February 1, 1983
Laryngeal oedema in pregnancy
A J Procter, J B White
Transfusion
|
June 24, 2000
Variations in genes encoding neutrophil antigens NA1 and NA2
K Matsuo, J Procter, D Stroncek
Angewandte Chemie (International Ed. in English)
|
September 24, 2017
Radical Heterocyclization and Heterocyclization Cascades Triggered by Electron Transfer to Amide-Type Carbonyl Compounds
Huan-Ming Huang, David J Procter
Angewandte Chemie (International Ed. in English)
|
March 1, 2013
Nucleophilic ortho-propargylation of aryl sulfoxides: an interrupted Pummerer/allenyl thio-Claisen rearrangement sequence
Andrew J Eberhart, David J Procter
Chemical Communications (Cambridge, England)
|
July 18, 2002
Reduction of alpha-aryloxy carbonyl compounds with samarium(II) iodide. A new traceless linker for the solid phase synthesis of carbonyl compounds
Fiona McKerlie, David J Procter, Graham Wynne
Organic Letters
|
January 26, 2012
Electron transfer reduction of carboxylic acids using SmI2-H2O-Et3N
Michal Szostak, Malcolm Spain, David J Procter
Journal of the American Chemical Society
|
May 10, 2014
Ketyl-type radicals from cyclic and acyclic esters are stabilized by SmI2(H2O)n: the role of SmI2(H2O)n in post-electron transfer steps
Michal Szostak, Malcolm Spain, David J Procter
Chemical Communications (Cambridge, England)
|
January 28, 2014
Structural analysis and reactivity of unusual tetrahedral intermediates enabled by SmI2-mediated reduction of barbituric acids: vinylogous N-acyliminium additions to α-hydroxy-N-acyl-carbamides
Michal Szostak, Brice Sautier, David J Procter
Page
of 20
Search research articles
Search
Showing results (11-20 of 200) with videos related to
Sort By:
Page
of 20
Accounts of Chemical Research
|
April 15, 2015
Sm(II)-Mediated Electron Transfer to Carboxylic Acid Derivatives: Development of Complexity-Generating Cascades
Xavier Just-Baringo, David J Procter
Angewandte Chemie (International Ed. in English)
|
July 14, 2016
C-H Coupling Reactions Directed by Sulfoxides: Teaching an Old Functional Group New Tricks
Alexander P Pulis, David J Procter
Anaesthesia
|
February 1, 1983
Laryngeal oedema in pregnancy
A J Procter, J B White
Transfusion
|
June 24, 2000
Variations in genes encoding neutrophil antigens NA1 and NA2
K Matsuo, J Procter, D Stroncek
Angewandte Chemie (International Ed. in English)
|
September 24, 2017
Radical Heterocyclization and Heterocyclization Cascades Triggered by Electron Transfer to Amide-Type Carbonyl Compounds
Huan-Ming Huang, David J Procter
Angewandte Chemie (International Ed. in English)
|
March 1, 2013
Nucleophilic ortho-propargylation of aryl sulfoxides: an interrupted Pummerer/allenyl thio-Claisen rearrangement sequence
Andrew J Eberhart, David J Procter
Chemical Communications (Cambridge, England)
|
July 18, 2002
Reduction of alpha-aryloxy carbonyl compounds with samarium(II) iodide. A new traceless linker for the solid phase synthesis of carbonyl compounds
Fiona McKerlie, David J Procter, Graham Wynne
Organic Letters
|
January 26, 2012
Electron transfer reduction of carboxylic acids using SmI2-H2O-Et3N
Michal Szostak, Malcolm Spain, David J Procter
Journal of the American Chemical Society
|
May 10, 2014
Ketyl-type radicals from cyclic and acyclic esters are stabilized by SmI2(H2O)n: the role of SmI2(H2O)n in post-electron transfer steps
Michal Szostak, Malcolm Spain, David J Procter
Chemical Communications (Cambridge, England)
|
January 28, 2014
Structural analysis and reactivity of unusual tetrahedral intermediates enabled by SmI2-mediated reduction of barbituric acids: vinylogous N-acyliminium additions to α-hydroxy-N-acyl-carbamides
Michal Szostak, Brice Sautier, David J Procter
Page
of 20