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

Michael S Sherburn

Showing results (1-10 of 76) with videos related to

Pageof 8
Sort By:
Accounts of Chemical Research|July 8, 2015
Preparation and synthetic value of π-bond-rich branched hydrocarbonsMichael S Sherburn
The Journal of Organic Chemistry|October 16, 2019
Diene-Transmissive Enantioselective Diels-Alder Reactions and Sequences Involving Substituted DendralenesJosemon George, Michael S Sherburn
Angewandte Chemie (International Ed. in English)|May 2, 2018
The Zipper-Mode Domino Intramolecular Diels-Alder Reaction: A New 0→ABCD Strategy for Steroids and Related CompoundsMarck Nörret, Michael S Sherburn
Angewandte Chemie (International Ed. in English)|February 17, 2012
Dendralenes branch out: cross-conjugated oligoenes allow the rapid generation of molecular complexityHenning Hopf, Michael S Sherburn
Chemistry (Weinheim an Der Bergstrasse, Germany)|October 18, 2014
Simple synthetic receptors for aspirinThanh V Nguyen, Michael S Sherburn
The Journal of Organic Chemistry|April 23, 2005
Single and double Suzuki-Miyaura couplings with symmetric dihalobenzenesDavid J Sinclair, Michael S Sherburn
Organic Letters|January 18, 2017
Four-Step Total Synthesis of Selaginpulvilin DMadison J Sowden, Michael S Sherburn
Natural Product Reports|April 18, 2015
Total synthesis of the pseudopterosin aglyconesChristopher G Newton, Michael S Sherburn
Chemical Communications (Cambridge, England)|July 6, 2005
Practical synthesis and guest-guest communication in multi-hemicarceplexesElizabeth S Barrett, Michael S Sherburn
Organic Letters|September 26, 2003
IMDA-radical cyclization approach to (+)-himbacineLeon S-M Wong, Michael S Sherburn
Pageof 8

Showing results (1-10 of 76) with videos related to

Sort By:
Pageof 8
Accounts of Chemical Research|July 8, 2015
Preparation and synthetic value of π-bond-rich branched hydrocarbonsMichael S Sherburn
The Journal of Organic Chemistry|October 16, 2019
Diene-Transmissive Enantioselective Diels-Alder Reactions and Sequences Involving Substituted DendralenesJosemon George, Michael S Sherburn
Angewandte Chemie (International Ed. in English)|May 2, 2018
The Zipper-Mode Domino Intramolecular Diels-Alder Reaction: A New 0→ABCD Strategy for Steroids and Related CompoundsMarck Nörret, Michael S Sherburn
Angewandte Chemie (International Ed. in English)|February 17, 2012
Dendralenes branch out: cross-conjugated oligoenes allow the rapid generation of molecular complexityHenning Hopf, Michael S Sherburn
Chemistry (Weinheim an Der Bergstrasse, Germany)|October 18, 2014
Simple synthetic receptors for aspirinThanh V Nguyen, Michael S Sherburn
The Journal of Organic Chemistry|April 23, 2005
Single and double Suzuki-Miyaura couplings with symmetric dihalobenzenesDavid J Sinclair, Michael S Sherburn
Organic Letters|January 18, 2017
Four-Step Total Synthesis of Selaginpulvilin DMadison J Sowden, Michael S Sherburn
Natural Product Reports|April 18, 2015
Total synthesis of the pseudopterosin aglyconesChristopher G Newton, Michael S Sherburn
Chemical Communications (Cambridge, England)|July 6, 2005
Practical synthesis and guest-guest communication in multi-hemicarceplexesElizabeth S Barrett, Michael S Sherburn
Organic Letters|September 26, 2003
IMDA-radical cyclization approach to (+)-himbacineLeon S-M Wong, Michael S Sherburn
Pageof 8