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

K N Houk

Showing results (71-80 of 897) with videos related to

Pageof 90
Sort By:
Molecular Physics|January 5, 2010
Origin of Substituent Effects in Edge-to-Face Aryl-Aryl InteractionsSteven E Wheeler, K N Houk
Chemistry & Biology|June 19, 2001
Canonical binding arrays as molecular recognition elements in the immune system: tetrahedral anions and the ester hydrolysis transition stateD J Tantillo, K N Houk
Angewandte Chemie (International Ed. in English)|February 22, 2003
Why trimerization? Computational elucidation of the origin of selective trimerization of ethene catalyzed by [TaCl3(CH3)2] and an agostic-assisted hydride transfer mechanismZhi-Xiang Yu, K N Houk
Chemical Communications (Cambridge, England)|July 12, 2002
Diels-Alder and ene reactions of singlet oxygen, nitroso compounds and triazolinediones: transition states and mechanisms from contemporary theoryAndrew G Leach, K N Houk
Journal of the American Chemical Society|December 16, 2016
Hyperconjugative, Secondary Orbital, Electrostatic, and Steric Effects on the Reactivities and Endo and Exo Stereoselectivities of Cyclopropene Diels-Alder ReactionsBrian J Levandowski, K N Houk
Journal of the American Chemical Society|July 26, 2008
Substituent effects in the benzene dimer are due to direct interactions of the substituents with the unsubstituted benzeneSteven E Wheeler, K N Houk
Journal of Chemical Theory and Computation|February 18, 2010
Through-Space Effects of Substituents Dominate Molecular Electrostatic Potentials of Substituted ArenesSteven E Wheeler, K N Houk
Journal of the American Chemical Society|August 10, 2007
Distortion/interaction energy control of 1,3-dipolar cycloaddition reactivityDaniel H Ess, K N Houk
Journal of the American Chemical Society|February 18, 2009
Substituent effects in cation/pi interactions and electrostatic potentials above the centers of substituted benzenes are due primarily to through-space effects of the substituentsSteven E Wheeler, K N Houk
The Journal of Organic Chemistry|September 13, 2014
Diels-Alder reactions of allene with benzene and butadiene: concerted, stepwise, and ambimodal transition statesHung V Pham, K N Houk
Pageof 90

Showing results (71-80 of 897) with videos related to

Sort By:
Pageof 90
Molecular Physics|January 5, 2010
Origin of Substituent Effects in Edge-to-Face Aryl-Aryl InteractionsSteven E Wheeler, K N Houk
Chemistry & Biology|June 19, 2001
Canonical binding arrays as molecular recognition elements in the immune system: tetrahedral anions and the ester hydrolysis transition stateD J Tantillo, K N Houk
Angewandte Chemie (International Ed. in English)|February 22, 2003
Why trimerization? Computational elucidation of the origin of selective trimerization of ethene catalyzed by [TaCl3(CH3)2] and an agostic-assisted hydride transfer mechanismZhi-Xiang Yu, K N Houk
Chemical Communications (Cambridge, England)|July 12, 2002
Diels-Alder and ene reactions of singlet oxygen, nitroso compounds and triazolinediones: transition states and mechanisms from contemporary theoryAndrew G Leach, K N Houk
Journal of the American Chemical Society|December 16, 2016
Hyperconjugative, Secondary Orbital, Electrostatic, and Steric Effects on the Reactivities and Endo and Exo Stereoselectivities of Cyclopropene Diels-Alder ReactionsBrian J Levandowski, K N Houk
Journal of the American Chemical Society|July 26, 2008
Substituent effects in the benzene dimer are due to direct interactions of the substituents with the unsubstituted benzeneSteven E Wheeler, K N Houk
Journal of Chemical Theory and Computation|February 18, 2010
Through-Space Effects of Substituents Dominate Molecular Electrostatic Potentials of Substituted ArenesSteven E Wheeler, K N Houk
Journal of the American Chemical Society|August 10, 2007
Distortion/interaction energy control of 1,3-dipolar cycloaddition reactivityDaniel H Ess, K N Houk
Journal of the American Chemical Society|February 18, 2009
Substituent effects in cation/pi interactions and electrostatic potentials above the centers of substituted benzenes are due primarily to through-space effects of the substituentsSteven E Wheeler, K N Houk
The Journal of Organic Chemistry|September 13, 2014
Diels-Alder reactions of allene with benzene and butadiene: concerted, stepwise, and ambimodal transition statesHung V Pham, K N Houk
Pageof 90