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Showing results (11-20 of 114) with videos related to

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Journal of the American Chemical Society|October 10, 2002
Remarkable activity of a novel cyclic seleninate ester as a glutathione peroxidase mimetic and its facile in situ generation from allyl 3-hydroxypropyl selenideThomas G Back, Ziad Moussa
The Journal of Organic Chemistry|October 22, 2014
Preparation of 1,7- and 3,9-dideazapurines from 2-amino-3-iodo- and 3-amino-4-iodopyridines and activated acetylenes by conjugate addition and copper-catalyzed intramolecular arylationYing Zhu, Thomas G Back
Journal of the American Chemical Society|October 30, 2003
Diselenides and allyl selenides as glutathione peroxidase mimetics. Remarkable activity of cyclic seleninates produced in situ by the oxidation of allyl omega-hydroxyalkyl selenidesThomas G Back, Ziad Moussa
Organic Letters|September 15, 2000
New chiral auxiliaries for highly stereoselective asymmetric methoxyselenenylationsT G Back, Z Moussa
Organic Letters|May 10, 2002
Total Synthesis of (-)-lasubine II by the conjugate addition and intramolecular acylation of an amino ester with an acetylenic sulfoneThomas G Back, Michael D Hamilton
Chemical Communications (Cambridge, England)|August 29, 2002
First syntheses of two quinoline alkaloids from the medicinal herb Ruta chalepensis via cyclization of an o-iodoaniline with an acetylenic sulfoneThomas G Back, Jeremy E Wulff
Organic Letters|July 12, 2011
Enhanced glutathione peroxidase activity of conformationally restricted naphthalene peri-dichalcogenidesDavid J Press, Thomas G Back
The Journal of Organic Chemistry|December 3, 1971
The synthesis of some new cysteine-containing unsymmetrical disulfidesD N Harpp, T G Back
Angewandte Chemie (International Ed. in English)|December 4, 2004
A stereodivergent synthesis of virantmycin by an enzyme-mediated diester desymmetrization and a highly hindered aryl aminationThomas G Back, Jeremy E Wulff
Organic Letters|July 25, 2000
A concise total synthesis of (+/-)-bakkenolide A by means of an intramolecular Diels-Alder reactionT G Back, J E Payne
Pageof 12

Showing results (11-20 of 114) with videos related to

Sort By:
Pageof 12
Journal of the American Chemical Society|October 10, 2002
Remarkable activity of a novel cyclic seleninate ester as a glutathione peroxidase mimetic and its facile in situ generation from allyl 3-hydroxypropyl selenideThomas G Back, Ziad Moussa
The Journal of Organic Chemistry|October 22, 2014
Preparation of 1,7- and 3,9-dideazapurines from 2-amino-3-iodo- and 3-amino-4-iodopyridines and activated acetylenes by conjugate addition and copper-catalyzed intramolecular arylationYing Zhu, Thomas G Back
Journal of the American Chemical Society|October 30, 2003
Diselenides and allyl selenides as glutathione peroxidase mimetics. Remarkable activity of cyclic seleninates produced in situ by the oxidation of allyl omega-hydroxyalkyl selenidesThomas G Back, Ziad Moussa
Organic Letters|September 15, 2000
New chiral auxiliaries for highly stereoselective asymmetric methoxyselenenylationsT G Back, Z Moussa
Organic Letters|May 10, 2002
Total Synthesis of (-)-lasubine II by the conjugate addition and intramolecular acylation of an amino ester with an acetylenic sulfoneThomas G Back, Michael D Hamilton
Chemical Communications (Cambridge, England)|August 29, 2002
First syntheses of two quinoline alkaloids from the medicinal herb Ruta chalepensis via cyclization of an o-iodoaniline with an acetylenic sulfoneThomas G Back, Jeremy E Wulff
Organic Letters|July 12, 2011
Enhanced glutathione peroxidase activity of conformationally restricted naphthalene peri-dichalcogenidesDavid J Press, Thomas G Back
The Journal of Organic Chemistry|December 3, 1971
The synthesis of some new cysteine-containing unsymmetrical disulfidesD N Harpp, T G Back
Angewandte Chemie (International Ed. in English)|December 4, 2004
A stereodivergent synthesis of virantmycin by an enzyme-mediated diester desymmetrization and a highly hindered aryl aminationThomas G Back, Jeremy E Wulff
Organic Letters|July 25, 2000
A concise total synthesis of (+/-)-bakkenolide A by means of an intramolecular Diels-Alder reactionT G Back, J E Payne
Pageof 12