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J Procter

Showing results (31-40 of 200) with videos related to

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Organic Letters|July 17, 2013
Nucleophilic ortho-allylation of pyrroles and pyrazoles: an accelerated Pummerer/thio-Claisen rearrangement sequenceAndrew J Eberhart, Claudio Cicoira, David J Procter
Vox Sanguinis|July 9, 2002
A novel method using formamide for the elution of antibodies from erythrocytesL Caruccio, K Byrne, J Procter, et al.
Chemical Science|September 30, 2017
Enantioselective copper catalysed, direct functionalisation of allenes <i>via</i> allyl copper intermediatesAlexander P Pulis, Kay Yeung, David J Procter
Organic & Biomolecular Chemistry|April 21, 2017
Selective construction of quaternary stereocentres in radical cyclisation cascades triggered by electron-transfer reduction of amide-type carbonylsHuan-Ming Huang, Pablo Bonilla, David J Procter
Organic Letters|September 5, 2008
A Samarium(II)-mediated, stereoselective cyclization for the synthesis of azaspirocyclesGiuditta Guazzelli, Lorna A Duffy, David J Procter
Journal of the American Chemical Society|January 11, 2008
A ring size-selective reduction of lactones using SmI2 and H2OLorna A Duffy, Hiroshi Matsubara, David J Procter
Beilstein Journal of Organic Chemistry|August 16, 2013
Development of an additive-controlled, SmI2-mediated stereoselective sequence: Telescoped spirocyclisation, lactone reduction and Peterson eliminationBrice Sautier, Karl D Collins, David J Procter
Anaesthesia|March 1, 1987
Spinal anaesthesia for Cesarean sectionN Hollis, J B White, A J Procter
Chemistry (Weinheim an Der Bergstrasse, Germany)|August 23, 2014
Cu(I)-NHC-catalyzed silylation of allenes: diastereoselective three-component coupling with aldehydesJames Rae, Ya Chu Hu, David J Procter
Chemical Reviews|July 15, 2004
Samarium(II)-iodide-mediated cyclizations in natural product synthesisDavid J Edmonds, Derek Johnston, David J Procter
Pageof 20

Showing results (31-40 of 200) with videos related to

Sort By:
Pageof 20
Organic Letters|July 17, 2013
Nucleophilic ortho-allylation of pyrroles and pyrazoles: an accelerated Pummerer/thio-Claisen rearrangement sequenceAndrew J Eberhart, Claudio Cicoira, David J Procter
Vox Sanguinis|July 9, 2002
A novel method using formamide for the elution of antibodies from erythrocytesL Caruccio, K Byrne, J Procter, et al.
Chemical Science|September 30, 2017
Enantioselective copper catalysed, direct functionalisation of allenes <i>via</i> allyl copper intermediatesAlexander P Pulis, Kay Yeung, David J Procter
Organic & Biomolecular Chemistry|April 21, 2017
Selective construction of quaternary stereocentres in radical cyclisation cascades triggered by electron-transfer reduction of amide-type carbonylsHuan-Ming Huang, Pablo Bonilla, David J Procter
Organic Letters|September 5, 2008
A Samarium(II)-mediated, stereoselective cyclization for the synthesis of azaspirocyclesGiuditta Guazzelli, Lorna A Duffy, David J Procter
Journal of the American Chemical Society|January 11, 2008
A ring size-selective reduction of lactones using SmI2 and H2OLorna A Duffy, Hiroshi Matsubara, David J Procter
Beilstein Journal of Organic Chemistry|August 16, 2013
Development of an additive-controlled, SmI2-mediated stereoselective sequence: Telescoped spirocyclisation, lactone reduction and Peterson eliminationBrice Sautier, Karl D Collins, David J Procter
Anaesthesia|March 1, 1987
Spinal anaesthesia for Cesarean sectionN Hollis, J B White, A J Procter
Chemistry (Weinheim an Der Bergstrasse, Germany)|August 23, 2014
Cu(I)-NHC-catalyzed silylation of allenes: diastereoselective three-component coupling with aldehydesJames Rae, Ya Chu Hu, David J Procter
Chemical Reviews|July 15, 2004
Samarium(II)-iodide-mediated cyclizations in natural product synthesisDavid J Edmonds, Derek Johnston, David J Procter
Pageof 20