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Organic Letters
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September 17, 2014
Copper-catalyzed one-pot synthesis of N-aryl oxazolidinones from amino alcohol carbamates
William Mahy, Pawel K Plucinski, Christopher G Frost
Organic & Biomolecular Chemistry
|
November 14, 2008
Rhodium catalysed conjugate addition of a chiral alkenyltrifluoroborate salt: the enantioselective synthesis of hermitamides A and B
Christopher G Frost, Stephen D Penrose, Robert Gleave
Organic Letters
|
May 26, 2009
Rhodium-catalyzed 1,4-additions to enantiopure acceptors: asymmetric synthesis of functionalized pyrrolizidinones
Ludivine Zoute, Gabriele Kociok-Köhn, Christopher G Frost
Molecules (Basel, Switzerland)
|
April 10, 2015
Trans-selective rhodium catalysed conjugate addition of organoboron reagents to dihydropyranones
Hannah J Edwards, Sean Goggins, Christopher G Frost
Chemical Communications (Cambridge, England)
|
August 8, 2008
Enantioselective rhodium-catalysed 1,4-additions of 2-heteroarylzinc donors using Me-DUPHOS
Jérôme Le Nôtre, Joseph C Allen, Christopher G Frost
Organic & Biomolecular Chemistry
|
October 25, 2011
Rhodium-catalysed enantioselective synthesis of 4-arylchroman-2-ones
Joseph C Allen, Gabriele Kociok-Köhn, Christopher G Frost
Dalton Transactions (Cambridge, England : 2003)
|
May 5, 2006
Structure and reactivity of new phosphine ligands containing the hemi-labile sulfone moiety
Christopher J Chapman, Christopher G Frost, Mary F Mahon
Chemistry, an Asian Journal
|
January 7, 2010
Alternatives to organoboron reagents in rhodium-catalyzed conjugate additions
Jonathan D Hargrave, Joseph C Allen, Christopher G Frost
Angewandte Chemie (International Ed. in English)
|
July 31, 2015
Ruthenium-Catalyzed O- to S-Alkyl Migration: A Pseudoreversible Barton-McCombie Pathway
William Mahy, Pawel Plucinski, Jesús Jover, et al.
Organic & Biomolecular Chemistry
|
October 13, 2006
Rhodium-catalysed addition of organotrialkoxysilanes to alpha-substituted acrylic esters
Jonathan D Hargrave, Jennifer Herbert, Gerwyn Bish, et al.
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Search research articles
Search
Showing results (11-20 of 53) with videos related to
Sort By:
Page
of 6
Organic Letters
|
September 17, 2014
Copper-catalyzed one-pot synthesis of N-aryl oxazolidinones from amino alcohol carbamates
William Mahy, Pawel K Plucinski, Christopher G Frost
Organic & Biomolecular Chemistry
|
November 14, 2008
Rhodium catalysed conjugate addition of a chiral alkenyltrifluoroborate salt: the enantioselective synthesis of hermitamides A and B
Christopher G Frost, Stephen D Penrose, Robert Gleave
Organic Letters
|
May 26, 2009
Rhodium-catalyzed 1,4-additions to enantiopure acceptors: asymmetric synthesis of functionalized pyrrolizidinones
Ludivine Zoute, Gabriele Kociok-Köhn, Christopher G Frost
Molecules (Basel, Switzerland)
|
April 10, 2015
Trans-selective rhodium catalysed conjugate addition of organoboron reagents to dihydropyranones
Hannah J Edwards, Sean Goggins, Christopher G Frost
Chemical Communications (Cambridge, England)
|
August 8, 2008
Enantioselective rhodium-catalysed 1,4-additions of 2-heteroarylzinc donors using Me-DUPHOS
Jérôme Le Nôtre, Joseph C Allen, Christopher G Frost
Organic & Biomolecular Chemistry
|
October 25, 2011
Rhodium-catalysed enantioselective synthesis of 4-arylchroman-2-ones
Joseph C Allen, Gabriele Kociok-Köhn, Christopher G Frost
Dalton Transactions (Cambridge, England : 2003)
|
May 5, 2006
Structure and reactivity of new phosphine ligands containing the hemi-labile sulfone moiety
Christopher J Chapman, Christopher G Frost, Mary F Mahon
Chemistry, an Asian Journal
|
January 7, 2010
Alternatives to organoboron reagents in rhodium-catalyzed conjugate additions
Jonathan D Hargrave, Joseph C Allen, Christopher G Frost
Angewandte Chemie (International Ed. in English)
|
July 31, 2015
Ruthenium-Catalyzed O- to S-Alkyl Migration: A Pseudoreversible Barton-McCombie Pathway
William Mahy, Pawel Plucinski, Jesús Jover, et al.
Organic & Biomolecular Chemistry
|
October 13, 2006
Rhodium-catalysed addition of organotrialkoxysilanes to alpha-substituted acrylic esters
Jonathan D Hargrave, Jennifer Herbert, Gerwyn Bish, et al.
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of 6