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

Catharine R Jones

Showing results (1-10 of 5) with videos related to

Pageof 1
Sort By:
Beilstein Journal of Organic Chemistry|March 31, 2011
Accuracy in determining interproton distances using Nuclear Overhauser Effect data from a flexible moleculeCatharine R Jones, Craig P Butts, Jeremy N Harvey
Chemical Communications (Cambridge, England)|November 27, 2010
High precision NOEs as a probe for low level conformers--a second conformation of strychnineCraig P Butts, Catharine R Jones, Jeremy N Harvey
Chemical Communications (Cambridge, England)|May 11, 2012
Accurate NOE-distance determination enables the stereochemical assignment of a flexible molecule--arugosin CCraig P Butts, Catharine R Jones, Zhongshu Song, et al.
Organic & Biomolecular Chemistry|November 3, 2010
Interproton distance determinations by NOE--surprising accuracy and precision in a rigid organic moleculeCraig P Butts, Catharine R Jones, Emma C Towers, et al.
The Journal of Organic Chemistry|December 29, 2011
Quantitative NMR-derived interproton distances combined with quantum mechanical calculations of 13C chemical shifts in the stereochemical determination of conicasterol F, a nuclear receptor ligand from Theonella swinhoeiMaria Giovanna Chini, Catharine R Jones, Angela Zampella, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Beilstein Journal of Organic Chemistry|March 31, 2011
Accuracy in determining interproton distances using Nuclear Overhauser Effect data from a flexible moleculeCatharine R Jones, Craig P Butts, Jeremy N Harvey
Chemical Communications (Cambridge, England)|November 27, 2010
High precision NOEs as a probe for low level conformers--a second conformation of strychnineCraig P Butts, Catharine R Jones, Jeremy N Harvey
Chemical Communications (Cambridge, England)|May 11, 2012
Accurate NOE-distance determination enables the stereochemical assignment of a flexible molecule--arugosin CCraig P Butts, Catharine R Jones, Zhongshu Song, et al.
Organic & Biomolecular Chemistry|November 3, 2010
Interproton distance determinations by NOE--surprising accuracy and precision in a rigid organic moleculeCraig P Butts, Catharine R Jones, Emma C Towers, et al.
The Journal of Organic Chemistry|December 29, 2011
Quantitative NMR-derived interproton distances combined with quantum mechanical calculations of 13C chemical shifts in the stereochemical determination of conicasterol F, a nuclear receptor ligand from Theonella swinhoeiMaria Giovanna Chini, Catharine R Jones, Angela Zampella, et al.
Pageof 1