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

Sheldon Hiebert

Showing results (1-10 of 11) with videos related to

Pageof 2
Sort By:
Journal of the American Chemical Society|February 5, 2004
Scope of palladium-catalyzed alkylative ring openingMark Lautens, Sheldon Hiebert
Accounts of Chemical Research|January 22, 2003
Transition metal-catalyzed enantioselective ring-opening reactions of oxabicyclic alkenesMark Lautens, Keith Fagnou, Sheldon Hiebert
Organic Letters|February 25, 2005
Toward an enantioselective total synthesis of sarain A: construction of an advanced intermediate and rearrangement of the sarain A core under mild conditionsChristopher J Douglas, Sheldon Hiebert, Larry E Overman
Organic Letters|May 25, 2002
Total synthesis of ionomycin using ring-opening strategiesMark Lautens, John T Colucci, Sheldon Hiebert, et al.
The Journal of Organic Chemistry|September 25, 2007
Synthesis of all low-energy stereoisomers of the tris(pyrrolidinoindoline) alkaloid hodgkinsine and preliminary assessment of their antinociceptive activityJeremy J Kodanko, Sheldon Hiebert, Emily A Peterson, et al.
Journal of the American Chemical Society|September 14, 2007
Total synthesis of (+)-sarain AMichael H Becker, Peter Chua, Robert Downham, et al.
Bioorganic & Medicinal Chemistry Letters|November 23, 2017
The discovery and optimization of naphthalene-linked P2-P4 Macrocycles as inhibitors of HCV NS3 proteaseMichael Bowsher, Sheldon Hiebert, Rongti Li, et al.
Chemmedchem|July 4, 2014
4-Benzothiazole-7-hydroxyindolinyl diaryl ureas are potent P2Y1 antagonists with favorable pharmacokinetics: low clearance and small volume of distributionJennifer X Qiao, Tammy C Wang, Sheldon Hiebert, et al.
Journal of Medicinal Chemistry|October 30, 2013
Conformationally constrained ortho-anilino diaryl ureas: discovery of 1-(2-(1'-neopentylspiro[indoline-3,4'-piperidine]-1-yl)phenyl)-3-(4-(trifluoromethoxy)phenyl)urea, a potent, selective, and bioavailable P2Y1 antagonistJennifer X Qiao, Tammy C Wang, Réjean Ruel, et al.
Journal of Medicinal Chemistry|November 23, 2020
Discovery of BMS-986144, a Third-Generation, Pan-Genotype NS3/4A Protease Inhibitor for the Treatment of Hepatitis C Virus InfectionLi-Qiang Sun, Eric Mull, Stanley D'Andrea, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Journal of the American Chemical Society|February 5, 2004
Scope of palladium-catalyzed alkylative ring openingMark Lautens, Sheldon Hiebert
Accounts of Chemical Research|January 22, 2003
Transition metal-catalyzed enantioselective ring-opening reactions of oxabicyclic alkenesMark Lautens, Keith Fagnou, Sheldon Hiebert
Organic Letters|February 25, 2005
Toward an enantioselective total synthesis of sarain A: construction of an advanced intermediate and rearrangement of the sarain A core under mild conditionsChristopher J Douglas, Sheldon Hiebert, Larry E Overman
Organic Letters|May 25, 2002
Total synthesis of ionomycin using ring-opening strategiesMark Lautens, John T Colucci, Sheldon Hiebert, et al.
The Journal of Organic Chemistry|September 25, 2007
Synthesis of all low-energy stereoisomers of the tris(pyrrolidinoindoline) alkaloid hodgkinsine and preliminary assessment of their antinociceptive activityJeremy J Kodanko, Sheldon Hiebert, Emily A Peterson, et al.
Journal of the American Chemical Society|September 14, 2007
Total synthesis of (+)-sarain AMichael H Becker, Peter Chua, Robert Downham, et al.
Bioorganic & Medicinal Chemistry Letters|November 23, 2017
The discovery and optimization of naphthalene-linked P2-P4 Macrocycles as inhibitors of HCV NS3 proteaseMichael Bowsher, Sheldon Hiebert, Rongti Li, et al.
Chemmedchem|July 4, 2014
4-Benzothiazole-7-hydroxyindolinyl diaryl ureas are potent P2Y1 antagonists with favorable pharmacokinetics: low clearance and small volume of distributionJennifer X Qiao, Tammy C Wang, Sheldon Hiebert, et al.
Journal of Medicinal Chemistry|October 30, 2013
Conformationally constrained ortho-anilino diaryl ureas: discovery of 1-(2-(1'-neopentylspiro[indoline-3,4'-piperidine]-1-yl)phenyl)-3-(4-(trifluoromethoxy)phenyl)urea, a potent, selective, and bioavailable P2Y1 antagonistJennifer X Qiao, Tammy C Wang, Réjean Ruel, et al.
Journal of Medicinal Chemistry|November 23, 2020
Discovery of BMS-986144, a Third-Generation, Pan-Genotype NS3/4A Protease Inhibitor for the Treatment of Hepatitis C Virus InfectionLi-Qiang Sun, Eric Mull, Stanley D'Andrea, et al.
Pageof 2