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

M Trost

Showing results (1-10 of 430) with videos related to

Pageof 43
Sort By:
Science (New York, N.Y.)|December 6, 1991
The atom economy--a search for synthetic efficiencyB M Trost
Accounts of Chemical Research|September 18, 2002
On inventing reactions for atom economyBarry M Trost
Chemical & Pharmaceutical Bulletin|February 5, 2002
Pd asymmetric allylic alkylation (AAA). A powerful synthetic toolBarry M Trost
Science (New York, N.Y.)|February 22, 1985
Sculpting horizons in organic chemistryB M Trost
Science (New York, N.Y.)|January 21, 1983
Selectivity: a key to synthetic efficiencyB M Trost
The Journal of Organic Chemistry|October 28, 2014
The toolbox of synthetic reactions: a key to unlock the design of structure for functionBarry M Trost
The Journal of Organic Chemistry|September 18, 2004
Asymmetric allylic alkylation, an enabling methodologyBarry M Trost
Angewandte Chemie (International Ed. in English)|March 14, 2012
Barry M. Trost. Interview by Stefan KirschBarry M Trost
Organic Process Research & Development|June 28, 2012
Pd and Mo Catalyzed Asymmetric Allylic AlkylationBarry M Trost
Tetrahedron|August 4, 2015
Metal Catalyzed Allylic Alkylation: Its Development in the Trost LaboratoriesBarry M Trost
Pageof 43

Showing results (1-10 of 430) with videos related to

Sort By:
Pageof 43
Science (New York, N.Y.)|December 6, 1991
The atom economy--a search for synthetic efficiencyB M Trost
Accounts of Chemical Research|September 18, 2002
On inventing reactions for atom economyBarry M Trost
Chemical & Pharmaceutical Bulletin|February 5, 2002
Pd asymmetric allylic alkylation (AAA). A powerful synthetic toolBarry M Trost
Science (New York, N.Y.)|February 22, 1985
Sculpting horizons in organic chemistryB M Trost
Science (New York, N.Y.)|January 21, 1983
Selectivity: a key to synthetic efficiencyB M Trost
The Journal of Organic Chemistry|October 28, 2014
The toolbox of synthetic reactions: a key to unlock the design of structure for functionBarry M Trost
The Journal of Organic Chemistry|September 18, 2004
Asymmetric allylic alkylation, an enabling methodologyBarry M Trost
Angewandte Chemie (International Ed. in English)|March 14, 2012
Barry M. Trost. Interview by Stefan KirschBarry M Trost
Organic Process Research & Development|June 28, 2012
Pd and Mo Catalyzed Asymmetric Allylic AlkylationBarry M Trost
Tetrahedron|August 4, 2015
Metal Catalyzed Allylic Alkylation: Its Development in the Trost LaboratoriesBarry M Trost
Pageof 43