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

Malcolm Spain

Showing results (11-20 of 26) with videos related to

Pageof 3
Sort By:
The Journal of Organic Chemistry|February 13, 2014
Determination of the effective redox potentials of SmI₂, SmBr₂, SmCl₂, and their complexes with water by reduction of aromatic hydrocarbons. Reduction of anthracene and stilbene by samarium(II) iodide-water complexMichal Szostak, Malcolm Spain, David J Procter
Organic Letters|October 25, 2014
Switching between reaction pathways by an alcohol cosolvent effect: SmI2-ethylene glycol vs SmI2-H2O mediated synthesis of uracilsMichal Szostak, Malcolm Spain, Brice Sautier, et al.
Organic Letters|February 6, 2014
Electron transfer reduction of nitriles using SmI2-Et3N-H2O: synthetic utility and mechanismMichal Szostak, Brice Sautier, Malcolm Spain, et al.
Chemical Communications (Cambridge, England)|September 1, 2011
Selective reductive transformations using samarium diiodide-waterMichal Szostak, Malcolm Spain, Dixit Parmar, et al.
Chemical Communications (Cambridge, England)|June 20, 2014
Mechanistic investigation of the selective reduction of Meldrum's acids to β-hydroxy acids using SmI2 and H2OMichal Szostak, Sarah E Lyons, Malcolm Spain, et al.
The Journal of Organic Chemistry|September 19, 2014
Mechanism of SmI2/amine/H2O-promoted chemoselective reductions of carboxylic acid derivatives (esters, acids, and amides) to alcoholsMichal Szostak, Malcolm Spain, Andrew J Eberhart, et al.
Journal of the American Chemical Society|January 28, 2014
Highly chemoselective reduction of amides (primary, secondary, tertiary) to alcohols using SmI2/amine/H2O under mild conditionsMichal Szostak, Malcolm Spain, Andrew J Eberhart, et al.
Journal of the American Chemical Society|July 4, 2012
Lactone radical cyclizations and cyclization cascades mediated by SmI2-H2ODixit Parmar, Hiroshi Matsubara, Kieran Price, et al.
Angewandte Chemie (International Ed. in English)|October 15, 2013
Selective reduction of barbituric acids using SmI2/H2O: synthesis, reactivity, and structural analysis of tetrahedral adductsMichal Szostak, Brice Sautier, Malcolm Spain, et al.
Journal of the American Chemical Society|October 2, 2013
Substrate-directable electron transfer reactions. Dramatic rate enhancement in the chemoselective reduction of cyclic esters using SmI2-H2O: mechanism, scope, and synthetic utilityMichal Szostak, Malcolm Spain, Kimberly A Choquette, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
The Journal of Organic Chemistry|February 13, 2014
Determination of the effective redox potentials of SmI₂, SmBr₂, SmCl₂, and their complexes with water by reduction of aromatic hydrocarbons. Reduction of anthracene and stilbene by samarium(II) iodide-water complexMichal Szostak, Malcolm Spain, David J Procter
Organic Letters|October 25, 2014
Switching between reaction pathways by an alcohol cosolvent effect: SmI2-ethylene glycol vs SmI2-H2O mediated synthesis of uracilsMichal Szostak, Malcolm Spain, Brice Sautier, et al.
Organic Letters|February 6, 2014
Electron transfer reduction of nitriles using SmI2-Et3N-H2O: synthetic utility and mechanismMichal Szostak, Brice Sautier, Malcolm Spain, et al.
Chemical Communications (Cambridge, England)|September 1, 2011
Selective reductive transformations using samarium diiodide-waterMichal Szostak, Malcolm Spain, Dixit Parmar, et al.
Chemical Communications (Cambridge, England)|June 20, 2014
Mechanistic investigation of the selective reduction of Meldrum's acids to β-hydroxy acids using SmI2 and H2OMichal Szostak, Sarah E Lyons, Malcolm Spain, et al.
The Journal of Organic Chemistry|September 19, 2014
Mechanism of SmI2/amine/H2O-promoted chemoselective reductions of carboxylic acid derivatives (esters, acids, and amides) to alcoholsMichal Szostak, Malcolm Spain, Andrew J Eberhart, et al.
Journal of the American Chemical Society|January 28, 2014
Highly chemoselective reduction of amides (primary, secondary, tertiary) to alcohols using SmI2/amine/H2O under mild conditionsMichal Szostak, Malcolm Spain, Andrew J Eberhart, et al.
Journal of the American Chemical Society|July 4, 2012
Lactone radical cyclizations and cyclization cascades mediated by SmI2-H2ODixit Parmar, Hiroshi Matsubara, Kieran Price, et al.
Angewandte Chemie (International Ed. in English)|October 15, 2013
Selective reduction of barbituric acids using SmI2/H2O: synthesis, reactivity, and structural analysis of tetrahedral adductsMichal Szostak, Brice Sautier, Malcolm Spain, et al.
Journal of the American Chemical Society|October 2, 2013
Substrate-directable electron transfer reactions. Dramatic rate enhancement in the chemoselective reduction of cyclic esters using SmI2-H2O: mechanism, scope, and synthetic utilityMichal Szostak, Malcolm Spain, Kimberly A Choquette, et al.
Pageof 3