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

Steven V Ley

Showing results (1-10 of 262) with videos related to

Pageof 27
Sort By:
Angewandte Chemie (International Ed. in English)|April 1, 2018
The Engineering of Chemical Synthesis: Humans and Machines Working in HarmonySteven V Ley
Topics in Current Chemistry|July 15, 2011
Concepts and strategies for oligosaccharide synthesis. ForewordSteven V Ley
Chemical Record (New York, N.Y.)|June 20, 2012
On being green: can flow chemistry help?Steven V Ley
Nature Reviews. Chemistry|December 10, 2025
A career with a natural interest in total synthesisSteven V Ley, Stephanie Greed
Angewandte Chemie (International Ed. in English)|October 19, 2002
Butane-2,3-diacetals of glyceraldehyde: a stable alternative to glyceraldehyde acetonidePatrick Michel, Steven V Ley
The Journal of Organic Chemistry|April 14, 2007
A fascination with 1,2-diacetalsSteven V Ley, Alessandra Polara
Organic & Biomolecular Chemistry|October 7, 2003
Reductive decomplexation of pi-allyltricarbonyliron lactone complexes using sodium naphthalenide as a route to stereodefined 1,7-diols and 2,3-diene-1,7-diolsChristopher J Hollowood, Steven V Ley
Chemical Record (New York, N.Y.)|December 7, 2002
Organic synthesis in a changing worldSteven V Ley, Ian R Baxendale
Bioorganic & Medicinal Chemistry Letters|June 28, 2002
A polymer-supported [1,3,2]oxazaphospholidine for the conversion of isothiocyanates to isocyanides and their subsequent use in an ugi reactionSteven V Ley, Stephen J Taylor
Journal of Combinatorial Chemistry|May 10, 2005
Formation of 4-aminopyrimidines via the trimerization of nitriles using focused microwave heatingIan R Baxendale, Steven V Ley
Pageof 27

Showing results (1-10 of 262) with videos related to

Sort By:
Pageof 27
Angewandte Chemie (International Ed. in English)|April 1, 2018
The Engineering of Chemical Synthesis: Humans and Machines Working in HarmonySteven V Ley
Topics in Current Chemistry|July 15, 2011
Concepts and strategies for oligosaccharide synthesis. ForewordSteven V Ley
Chemical Record (New York, N.Y.)|June 20, 2012
On being green: can flow chemistry help?Steven V Ley
Nature Reviews. Chemistry|December 10, 2025
A career with a natural interest in total synthesisSteven V Ley, Stephanie Greed
Angewandte Chemie (International Ed. in English)|October 19, 2002
Butane-2,3-diacetals of glyceraldehyde: a stable alternative to glyceraldehyde acetonidePatrick Michel, Steven V Ley
The Journal of Organic Chemistry|April 14, 2007
A fascination with 1,2-diacetalsSteven V Ley, Alessandra Polara
Organic & Biomolecular Chemistry|October 7, 2003
Reductive decomplexation of pi-allyltricarbonyliron lactone complexes using sodium naphthalenide as a route to stereodefined 1,7-diols and 2,3-diene-1,7-diolsChristopher J Hollowood, Steven V Ley
Chemical Record (New York, N.Y.)|December 7, 2002
Organic synthesis in a changing worldSteven V Ley, Ian R Baxendale
Bioorganic & Medicinal Chemistry Letters|June 28, 2002
A polymer-supported [1,3,2]oxazaphospholidine for the conversion of isothiocyanates to isocyanides and their subsequent use in an ugi reactionSteven V Ley, Stephen J Taylor
Journal of Combinatorial Chemistry|May 10, 2005
Formation of 4-aminopyrimidines via the trimerization of nitriles using focused microwave heatingIan R Baxendale, Steven V Ley
Pageof 27