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Bioorganic & Medicinal Chemistry
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March 27, 2020
Synthesis and evaluation of the performance of a small molecule library based on diverse tropane-related scaffolds
Robert A Lowe, Dale Taylor, Kelly Chibale, et al.
The Journal of Organic Chemistry
|
September 25, 2004
Reagent-controlled stereoselective synthesis of lignan-related tetrahydrofurans
Steven M Miles, Stephen P Marsden, Robin J Leatherbarrow, et al.
Organic Letters
|
October 6, 2017
Direct Synthesis of N-Alkyl Arylglycines by Organocatalytic Asymmetric Transfer Hydrogenation of N-Alkyl Aryl Imino Esters
Javier Mazuela, Thomas Antonsson, Magnus J Johansson, et al.
Organic & Biomolecular Chemistry
|
January 30, 2004
Synthesis and bio-assay of RCM-derived Bowman-Birk inhibitor analogues
Steven M Miles, Robin J Leatherbarrow, Stephen P Marsden, et al.
Chemical Communications (Cambridge, England)
|
October 19, 2004
A novel, stereoselective and convergent synthesis of aryltetralins
Steven M Miles, Stephen P Marsden, Robin J Leatherbarrow, et al.
Organic Letters
|
August 30, 2008
Convergent, regiospecific synthesis of quinolines from o-aminophenylboronates
Joachim Horn, Stephen P Marsden, Adam Nelson, et al.
The Journal of Organic Chemistry
|
May 14, 2011
Catalyst control in sequential asymmetric allylic substitution: stereodivergent access to N,N-diprotected unnatural amino acids
Paolo Tosatti, Amanda J Campbell, David House, et al.
Organic Letters
|
November 18, 2005
Deconjugation of dehydroamino acids: stereoselective synthesis of racemic (E)-vinylglycines
Paul A Alexander, Stephen P Marsden, Dulce M Muñoz Subtil, et al.
Chemical Communications (Cambridge, England)
|
May 27, 2015
A systematic approach to diverse, lead-like scaffolds from α,α-disubstituted amino acids
Daniel J Foley, Richard G Doveston, Ian Churcher, et al.
Chemical Communications (Cambridge, England)
|
July 7, 2020
Fragment-oriented synthesis: β-elaboration of cyclic amine fragments using enecarbamates as platform intermediates
Alexandre F Trindade, Emily L Faulkner, Andrew G Leach, et al.
Page
of 7
Search research articles
Search
Showing results (31-40 of 62) with videos related to
Sort By:
Page
of 7
Bioorganic & Medicinal Chemistry
|
March 27, 2020
Synthesis and evaluation of the performance of a small molecule library based on diverse tropane-related scaffolds
Robert A Lowe, Dale Taylor, Kelly Chibale, et al.
The Journal of Organic Chemistry
|
September 25, 2004
Reagent-controlled stereoselective synthesis of lignan-related tetrahydrofurans
Steven M Miles, Stephen P Marsden, Robin J Leatherbarrow, et al.
Organic Letters
|
October 6, 2017
Direct Synthesis of N-Alkyl Arylglycines by Organocatalytic Asymmetric Transfer Hydrogenation of N-Alkyl Aryl Imino Esters
Javier Mazuela, Thomas Antonsson, Magnus J Johansson, et al.
Organic & Biomolecular Chemistry
|
January 30, 2004
Synthesis and bio-assay of RCM-derived Bowman-Birk inhibitor analogues
Steven M Miles, Robin J Leatherbarrow, Stephen P Marsden, et al.
Chemical Communications (Cambridge, England)
|
October 19, 2004
A novel, stereoselective and convergent synthesis of aryltetralins
Steven M Miles, Stephen P Marsden, Robin J Leatherbarrow, et al.
Organic Letters
|
August 30, 2008
Convergent, regiospecific synthesis of quinolines from o-aminophenylboronates
Joachim Horn, Stephen P Marsden, Adam Nelson, et al.
The Journal of Organic Chemistry
|
May 14, 2011
Catalyst control in sequential asymmetric allylic substitution: stereodivergent access to N,N-diprotected unnatural amino acids
Paolo Tosatti, Amanda J Campbell, David House, et al.
Organic Letters
|
November 18, 2005
Deconjugation of dehydroamino acids: stereoselective synthesis of racemic (E)-vinylglycines
Paul A Alexander, Stephen P Marsden, Dulce M Muñoz Subtil, et al.
Chemical Communications (Cambridge, England)
|
May 27, 2015
A systematic approach to diverse, lead-like scaffolds from α,α-disubstituted amino acids
Daniel J Foley, Richard G Doveston, Ian Churcher, et al.
Chemical Communications (Cambridge, England)
|
July 7, 2020
Fragment-oriented synthesis: β-elaboration of cyclic amine fragments using enecarbamates as platform intermediates
Alexandre F Trindade, Emily L Faulkner, Andrew G Leach, et al.
Page
of 7