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Michael P Jennings

Showing results (11-20 of 251) with videos related to

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The Journal of Organic Chemistry|June 23, 2021
Stereoselective Halo-Succinimide Facilitated α-Halogenations of Substituted α-Trialkylsilyl-β-Substituted-α,β-Unsaturated EstersKristina C Probasco, Michael P Jennings
Organic Letters|September 15, 2018
Tandem Copper-Catalyzed Conjugate Addition-Diastereoselective Protonation of ( E)-α-Trialkylsilyl-β-Alkyl(Aryl)-α,β-Unsaturated EstersDavid A Johnson, Michael P Jennings
The Journal of Organic Chemistry|May 27, 2010
Formal synthesis of (-)-neopeltolide featuring a highly stereoselective oxocarbenium formation/reduction sequenceDionicio Martinez-Solorio, Michael P Jennings
Chemical Communications (Cambridge, England)|June 21, 2006
An efficient total synthesis and absolute configuration determination of varitriolRyan T Clemens, Michael P Jennings
The Journal of Organic Chemistry|September 26, 2006
Efficient total syntheses and structural verification of both diospongins A and B via a common delta-lactone intermediateKailas B Sawant, Michael P Jennings
Biochemical and Biophysical Research Communications|February 13, 2007
Experimental confirmation of a key role for non-optimal codons in protein exportYaramah M Zalucki, Michael P Jennings
Organic Letters|November 16, 2007
A highly stereoselective TMSOTf-mediated catalytic carbocupration of alkynoatesAmanda J Mueller, Michael P Jennings
Organic Letters|January 8, 2009
An efficient formal synthesis of (-)-clavosolide a featuring a "mismatched" stereoselective oxocarbenium reductionJesse D Carrick, Michael P Jennings
The Journal of Organic Chemistry|July 17, 2007
Total synthesis and absolute configuration determination of (+)-bruguierol CDionicio Martinez Solorio, Michael P Jennings
The Journal of Organic Chemistry|July 26, 2012
Syntheses of (-)-cryptocaryolone and (-)-cryptocaryolone diacetate via a diastereoselective oxy-Michael addition and oxocarbenium allylationAymara M M Albury, Michael P Jennings
Pageof 26

Showing results (11-20 of 251) with videos related to

Sort By:
Pageof 26
The Journal of Organic Chemistry|June 23, 2021
Stereoselective Halo-Succinimide Facilitated α-Halogenations of Substituted α-Trialkylsilyl-β-Substituted-α,β-Unsaturated EstersKristina C Probasco, Michael P Jennings
Organic Letters|September 15, 2018
Tandem Copper-Catalyzed Conjugate Addition-Diastereoselective Protonation of ( E)-α-Trialkylsilyl-β-Alkyl(Aryl)-α,β-Unsaturated EstersDavid A Johnson, Michael P Jennings
The Journal of Organic Chemistry|May 27, 2010
Formal synthesis of (-)-neopeltolide featuring a highly stereoselective oxocarbenium formation/reduction sequenceDionicio Martinez-Solorio, Michael P Jennings
Chemical Communications (Cambridge, England)|June 21, 2006
An efficient total synthesis and absolute configuration determination of varitriolRyan T Clemens, Michael P Jennings
The Journal of Organic Chemistry|September 26, 2006
Efficient total syntheses and structural verification of both diospongins A and B via a common delta-lactone intermediateKailas B Sawant, Michael P Jennings
Biochemical and Biophysical Research Communications|February 13, 2007
Experimental confirmation of a key role for non-optimal codons in protein exportYaramah M Zalucki, Michael P Jennings
Organic Letters|November 16, 2007
A highly stereoselective TMSOTf-mediated catalytic carbocupration of alkynoatesAmanda J Mueller, Michael P Jennings
Organic Letters|January 8, 2009
An efficient formal synthesis of (-)-clavosolide a featuring a "mismatched" stereoselective oxocarbenium reductionJesse D Carrick, Michael P Jennings
The Journal of Organic Chemistry|July 17, 2007
Total synthesis and absolute configuration determination of (+)-bruguierol CDionicio Martinez Solorio, Michael P Jennings
The Journal of Organic Chemistry|July 26, 2012
Syntheses of (-)-cryptocaryolone and (-)-cryptocaryolone diacetate via a diastereoselective oxy-Michael addition and oxocarbenium allylationAymara M M Albury, Michael P Jennings
Pageof 26