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Rudolf Knorr

Showing results (1-10 of 14) with videos related to

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Chemical Reviews|September 9, 2004
Alkylidenecarbenes, alkylidenecarbenoids, and competing species: which is responsible for vinylic nucleophilic substitution, [1 + 2] cycloadditions, 1,5-CH insertions, and the Fritsch-Buttenberg-Wiechell rearrangement?Rudolf Knorr
Beilstein Journal of Organic Chemistry|December 29, 2018
Nucleofugal behavior of a β-shielded α-cyanovinyl carbanionRudolf Knorr, Barbara Schmidt
Chemistry (Weinheim an Der Bergstrasse, Germany)|May 9, 2012
Deuterium quantification through deuterium-induced remote 1H and 13C NMR shiftsRudolf Knorr, David S Stephenson
The Journal of Organic Chemistry|July 13, 2007
Carbenoid chain reactions through proton, deuteron, or bromine transfer from unactivated 1-bromo-1-alkenes to organolithium compoundsRudolf Knorr, Claudio Pires, Johannes Freudenreich
Beilstein Journal of Organic Chemistry|November 11, 2014
Microsolvation and sp(2)-stereoinversion of monomeric α-(2,6-di-tert-butylphenyl)vinyllithium as measured by NMRRudolf Knorr, Monika Knittl, Eva C Rossmann
Beilstein Journal of Organic Chemistry|March 11, 2014
Carbenoid-mediated nucleophilic "hydrolysis" of 2-(dichloromethylidene)-1,1,3,3-tetramethylindane with DMSO participation, affording access to one-sidedly overcrowded ketone and bromoalkene descendants(§)Rudolf Knorr, Thomas Menke, Johannes Freudenreich, et al.
The Journal of Organic Chemistry|February 11, 2017
Kinetics of α-(2,6-Dimethylphenl)vinyllithium: How To Control Errors Caused by Inefficient Mixing with Pairs of Rapidly Competing KetonesRudolf Knorr, Monika Knittl, Claudia Behringer, et al.
The Journal of Organic Chemistry|June 2, 2015
How Microsolvation Numbers at Li Control Aggregation Modes, sp(2)-Stereoinversion, and NMR Coupling Constants (2)JH,H of H2C═C in α-(2,6-Dimethylphenyl)vinyllithiumRudolf Knorr, Claudia Behringer, Ernst Lattke, et al.
Journal of the American Chemical Society|March 4, 2017
Doubly Diastereoconvergent Preparation and Microsolvation-Controlled Properties of (Z)- and (E)-1'-Lithio-1'-(2,6-dimethylphenyl)propenesRudolf Knorr, Claudia Behringer, Monika Knittl, et al.
Beilstein Journal of Organic Chemistry|August 26, 2016
Unusual traits of cis and trans-2,3-dibromo-1,1-dimethylindane on the way from 1,1-dimethylindene to 2-bromo-, 3-bromo-, and 2,3-dibromo-1,1-dimethylindeneRudolf Knorr, David S Stephenson, Ernst Lattke, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Chemical Reviews|September 9, 2004
Alkylidenecarbenes, alkylidenecarbenoids, and competing species: which is responsible for vinylic nucleophilic substitution, [1 + 2] cycloadditions, 1,5-CH insertions, and the Fritsch-Buttenberg-Wiechell rearrangement?Rudolf Knorr
Beilstein Journal of Organic Chemistry|December 29, 2018
Nucleofugal behavior of a β-shielded α-cyanovinyl carbanionRudolf Knorr, Barbara Schmidt
Chemistry (Weinheim an Der Bergstrasse, Germany)|May 9, 2012
Deuterium quantification through deuterium-induced remote 1H and 13C NMR shiftsRudolf Knorr, David S Stephenson
The Journal of Organic Chemistry|July 13, 2007
Carbenoid chain reactions through proton, deuteron, or bromine transfer from unactivated 1-bromo-1-alkenes to organolithium compoundsRudolf Knorr, Claudio Pires, Johannes Freudenreich
Beilstein Journal of Organic Chemistry|November 11, 2014
Microsolvation and sp(2)-stereoinversion of monomeric α-(2,6-di-tert-butylphenyl)vinyllithium as measured by NMRRudolf Knorr, Monika Knittl, Eva C Rossmann
Beilstein Journal of Organic Chemistry|March 11, 2014
Carbenoid-mediated nucleophilic "hydrolysis" of 2-(dichloromethylidene)-1,1,3,3-tetramethylindane with DMSO participation, affording access to one-sidedly overcrowded ketone and bromoalkene descendants(§)Rudolf Knorr, Thomas Menke, Johannes Freudenreich, et al.
The Journal of Organic Chemistry|February 11, 2017
Kinetics of α-(2,6-Dimethylphenl)vinyllithium: How To Control Errors Caused by Inefficient Mixing with Pairs of Rapidly Competing KetonesRudolf Knorr, Monika Knittl, Claudia Behringer, et al.
The Journal of Organic Chemistry|June 2, 2015
How Microsolvation Numbers at Li Control Aggregation Modes, sp(2)-Stereoinversion, and NMR Coupling Constants (2)JH,H of H2C═C in α-(2,6-Dimethylphenyl)vinyllithiumRudolf Knorr, Claudia Behringer, Ernst Lattke, et al.
Journal of the American Chemical Society|March 4, 2017
Doubly Diastereoconvergent Preparation and Microsolvation-Controlled Properties of (Z)- and (E)-1'-Lithio-1'-(2,6-dimethylphenyl)propenesRudolf Knorr, Claudia Behringer, Monika Knittl, et al.
Beilstein Journal of Organic Chemistry|August 26, 2016
Unusual traits of cis and trans-2,3-dibromo-1,1-dimethylindane on the way from 1,1-dimethylindene to 2-bromo-, 3-bromo-, and 2,3-dibromo-1,1-dimethylindeneRudolf Knorr, David S Stephenson, Ernst Lattke, et al.
Pageof 2