Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Martin Wills

Showing results (31-40 of 76) with videos related to

Pageof 8
Sort By:
Dalton Transactions (Cambridge, England : 2003)|February 4, 2016
Iron cyclopentadienone complexes derived from C2-symmetric bis-propargylic alcohols; preparation and applications to catalysisRoy Hodgkinson, Alessandro Del Grosso, Guy Clarkson, et al.
Organic Letters|September 28, 2013
Direct formation of tethered Ru(II) catalysts using arene exchangeRina Soni, Katherine E Jolley, Guy J Clarkson, et al.
Organic Letters|July 16, 2011
An unexpected directing effect in the asymmetric transfer hydrogenation of α,α-disubstituted ketonesRina Soni, John-Michael Collinson, Guy C Clarkson, et al.
ACS Chemical Biology|August 30, 2013
Structure and mechanism of acetolactate decarboxylaseVictoria A Marlow, Dean Rea, Shabir Najmudin, et al.
Organic Letters|February 1, 2018
Combining Electronic and Steric Effects To Generate Hindered Propargylic Alcohols in High Enantiomeric ExcessVijyesh K Vyas, Richard C Knighton, Bhalchandra M Bhanage, et al.
Chemical Communications (Cambridge, England)|October 10, 2006
An outstanding catalyst for asymmetric transfer hydrogenation in aqueous solution and formic acid/triethylamineDaljit S Matharu, David J Morris, Guy J Clarkson, et al.
Journal of the American Chemical Society|May 19, 2005
A class of ruthenium(II) catalyst for asymmetric transfer hydrogenations of ketonesAidan M Hayes, David J Morris, Guy J Clarkson, et al.
Organic Letters|September 29, 2021
Asymmetric Transfer Hydrogenation of α-Keto Amides; Highly Enantioselective Formation of Malic Acid Diamides and α-HydroxyamidesShweta K Gediya, Vijyesh K Vyas, Guy J Clarkson, et al.
Physical Chemistry Chemical Physics : PCCP|February 27, 2023
Examining the substituent effect on mycosporine-inspired ultraviolet filtersAbigail L Whittock, Adam M Cowden, Martin Wills, et al.
Organic Letters|October 24, 2003
A one-pot process for the enantioselective synthesis of amines via reductive amination under transfer hydrogenation conditionsGlynn D Williams, Richard A Pike, Charles E Wade, et al.
Pageof 8

Showing results (31-40 of 76) with videos related to

Sort By:
Pageof 8
Dalton Transactions (Cambridge, England : 2003)|February 4, 2016
Iron cyclopentadienone complexes derived from C2-symmetric bis-propargylic alcohols; preparation and applications to catalysisRoy Hodgkinson, Alessandro Del Grosso, Guy Clarkson, et al.
Organic Letters|September 28, 2013
Direct formation of tethered Ru(II) catalysts using arene exchangeRina Soni, Katherine E Jolley, Guy J Clarkson, et al.
Organic Letters|July 16, 2011
An unexpected directing effect in the asymmetric transfer hydrogenation of α,α-disubstituted ketonesRina Soni, John-Michael Collinson, Guy C Clarkson, et al.
ACS Chemical Biology|August 30, 2013
Structure and mechanism of acetolactate decarboxylaseVictoria A Marlow, Dean Rea, Shabir Najmudin, et al.
Organic Letters|February 1, 2018
Combining Electronic and Steric Effects To Generate Hindered Propargylic Alcohols in High Enantiomeric ExcessVijyesh K Vyas, Richard C Knighton, Bhalchandra M Bhanage, et al.
Chemical Communications (Cambridge, England)|October 10, 2006
An outstanding catalyst for asymmetric transfer hydrogenation in aqueous solution and formic acid/triethylamineDaljit S Matharu, David J Morris, Guy J Clarkson, et al.
Journal of the American Chemical Society|May 19, 2005
A class of ruthenium(II) catalyst for asymmetric transfer hydrogenations of ketonesAidan M Hayes, David J Morris, Guy J Clarkson, et al.
Organic Letters|September 29, 2021
Asymmetric Transfer Hydrogenation of α-Keto Amides; Highly Enantioselective Formation of Malic Acid Diamides and α-HydroxyamidesShweta K Gediya, Vijyesh K Vyas, Guy J Clarkson, et al.
Physical Chemistry Chemical Physics : PCCP|February 27, 2023
Examining the substituent effect on mycosporine-inspired ultraviolet filtersAbigail L Whittock, Adam M Cowden, Martin Wills, et al.
Organic Letters|October 24, 2003
A one-pot process for the enantioselective synthesis of amines via reductive amination under transfer hydrogenation conditionsGlynn D Williams, Richard A Pike, Charles E Wade, et al.
Pageof 8