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

Scott D Rychnovsky

Showing results (31-40 of 125) with videos related to

Pageof 13
Sort By:
Organic Letters|May 7, 2005
Reductive spiroannulation of nitriles with secondary electrophilesMatthew D Morin, Scott D Rychnovsky
Organic Letters|October 17, 2013
Kinetic analysis of the HBTM-catalyzed esterification of an enantiopure secondary alcoholAlexander J Wagner, Scott D Rychnovsky
Natural Product Reports|December 6, 2014
Generation, structure and reactivity of tertiary organolithium reagentsMatthew A Perry, Scott D Rychnovsky
The Journal of Organic Chemistry|March 14, 2008
A concise synthesis of ent-CholesterolJitendra D Belani, Scott D Rychnovsky
Angewandte Chemie (International Ed. in English)|March 20, 2003
Unified strategy for the synthesis of (-)-elisapterosin B and (-)-colombiasin AAngie I Kim, Scott D Rychnovsky
Journal of the American Chemical Society|September 5, 2008
Formal synthesis of (-)-kendomycin featuring a Prins-cyclization to construct the macrocycleKevin B Bahnck, Scott D Rychnovsky
Organic Letters|July 30, 2004
Generation and utility of tertiary alpha-aminoorganolithium reagentsScott A Wolckenhauer, Scott D Rychnovsky
Organic Letters|April 9, 2005
Enantioselective synthesis of the C18-C25 segment of lasonolide A by an oxonia-cope prins cascadeJackline E Dalgard, Scott D Rychnovsky
Journal of the American Chemical Society|December 2, 2004
Oxonia-cope prins cyclizations: a facile method for the synthesis of tetrahydropyranones bearing quaternary centersJackline E Dalgard, Scott D Rychnovsky
The Journal of Organic Chemistry|April 19, 2013
Determination of absolute configuration of secondary alcohols using thin-layer chromatographyAlexander J Wagner, Scott D Rychnovsky
Pageof 13

Showing results (31-40 of 125) with videos related to

Sort By:
Pageof 13
Organic Letters|May 7, 2005
Reductive spiroannulation of nitriles with secondary electrophilesMatthew D Morin, Scott D Rychnovsky
Organic Letters|October 17, 2013
Kinetic analysis of the HBTM-catalyzed esterification of an enantiopure secondary alcoholAlexander J Wagner, Scott D Rychnovsky
Natural Product Reports|December 6, 2014
Generation, structure and reactivity of tertiary organolithium reagentsMatthew A Perry, Scott D Rychnovsky
The Journal of Organic Chemistry|March 14, 2008
A concise synthesis of ent-CholesterolJitendra D Belani, Scott D Rychnovsky
Angewandte Chemie (International Ed. in English)|March 20, 2003
Unified strategy for the synthesis of (-)-elisapterosin B and (-)-colombiasin AAngie I Kim, Scott D Rychnovsky
Journal of the American Chemical Society|September 5, 2008
Formal synthesis of (-)-kendomycin featuring a Prins-cyclization to construct the macrocycleKevin B Bahnck, Scott D Rychnovsky
Organic Letters|July 30, 2004
Generation and utility of tertiary alpha-aminoorganolithium reagentsScott A Wolckenhauer, Scott D Rychnovsky
Organic Letters|April 9, 2005
Enantioselective synthesis of the C18-C25 segment of lasonolide A by an oxonia-cope prins cascadeJackline E Dalgard, Scott D Rychnovsky
Journal of the American Chemical Society|December 2, 2004
Oxonia-cope prins cyclizations: a facile method for the synthesis of tetrahydropyranones bearing quaternary centersJackline E Dalgard, Scott D Rychnovsky
The Journal of Organic Chemistry|April 19, 2013
Determination of absolute configuration of secondary alcohols using thin-layer chromatographyAlexander J Wagner, Scott D Rychnovsky
Pageof 13