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Shahien Shahsavari

Showing results (1-10 of 12) with videos related to

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Chemistryselect|November 4, 2017
Formation of Hindered Arylcarbamates using Alkyl Aryl Carbonates under Highly Reactive ConditionsShahien Shahsavari, James Gooding, Travis Wigstrom, et al.
Tetrahedron Letters|October 3, 2018
dM-Dim for Carboxylic Acid ProtectionShahien Shahsavari, Travis Wigstrom, James Gooding, et al.
Organic Letters|July 23, 2016
Synthesis of Oligodeoxynucleotides Containing Electrophilic GroupsXi Lin, Jinsen Chen, Shahien Shahsavari, et al.
Tetrahedron Letters|January 3, 2017
Tritylation of Alcohols under Mild Conditions without Using Silver SaltsShahien Shahsavari, Jinsen Chen, Travis Wigstrom, et al.
Current Protocols in Nucleic Acid Chemistry|July 7, 2020
Dim and Dmoc Protecting Groups for Oligodeoxynucleotide SynthesisShiyue Fang, Dhananjani Eriyagama, Yinan Yuan, et al.
Beilstein Journal of Organic Chemistry|August 17, 2018
An amine protecting group deprotectable under nearly neutral oxidative conditionsShahien Shahsavari, Chase McNamara, Mark Sylvester, et al.
Chemistryselect|March 20, 2019
Incorporation of Sensitive Ester and Chloropurine Groups into Oligodeoxynucleotides through Solid Phase SynthesisBhaskar Halami, Shahien Shahsavari, Zack Nelson, et al.
Organic Process Research & Development|March 26, 2019
Parallel, Large-Scale, and Long Synthetic Oligodeoxynucleotide Purification Using the Catching Full-Length Sequence by Polymerization TechniqueDhananjani N A M Eriyagama, Shahien Shahsavari, Bhaskar Halami, et al.
The Journal of Organic Chemistry|September 20, 2019
Sensitive Oligodeoxynucleotide Synthesis Using Dim and Dmoc as Protecting GroupsShahien Shahsavari, Dhananjani N A M Eriyagama, Jinsen Chen, et al.
New Journal of Chemistry = Nouveau Journal De Chimie|November 2, 2023
Oligonucleotide synthesis under mild deprotection conditionsKomal Chillar, Adikari M D N Eriyagama, Yipeng Yin, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Chemistryselect|November 4, 2017
Formation of Hindered Arylcarbamates using Alkyl Aryl Carbonates under Highly Reactive ConditionsShahien Shahsavari, James Gooding, Travis Wigstrom, et al.
Tetrahedron Letters|October 3, 2018
dM-Dim for Carboxylic Acid ProtectionShahien Shahsavari, Travis Wigstrom, James Gooding, et al.
Organic Letters|July 23, 2016
Synthesis of Oligodeoxynucleotides Containing Electrophilic GroupsXi Lin, Jinsen Chen, Shahien Shahsavari, et al.
Tetrahedron Letters|January 3, 2017
Tritylation of Alcohols under Mild Conditions without Using Silver SaltsShahien Shahsavari, Jinsen Chen, Travis Wigstrom, et al.
Current Protocols in Nucleic Acid Chemistry|July 7, 2020
Dim and Dmoc Protecting Groups for Oligodeoxynucleotide SynthesisShiyue Fang, Dhananjani Eriyagama, Yinan Yuan, et al.
Beilstein Journal of Organic Chemistry|August 17, 2018
An amine protecting group deprotectable under nearly neutral oxidative conditionsShahien Shahsavari, Chase McNamara, Mark Sylvester, et al.
Chemistryselect|March 20, 2019
Incorporation of Sensitive Ester and Chloropurine Groups into Oligodeoxynucleotides through Solid Phase SynthesisBhaskar Halami, Shahien Shahsavari, Zack Nelson, et al.
Organic Process Research & Development|March 26, 2019
Parallel, Large-Scale, and Long Synthetic Oligodeoxynucleotide Purification Using the Catching Full-Length Sequence by Polymerization TechniqueDhananjani N A M Eriyagama, Shahien Shahsavari, Bhaskar Halami, et al.
The Journal of Organic Chemistry|September 20, 2019
Sensitive Oligodeoxynucleotide Synthesis Using Dim and Dmoc as Protecting GroupsShahien Shahsavari, Dhananjani N A M Eriyagama, Jinsen Chen, et al.
New Journal of Chemistry = Nouveau Journal De Chimie|November 2, 2023
Oligonucleotide synthesis under mild deprotection conditionsKomal Chillar, Adikari M D N Eriyagama, Yipeng Yin, et al.
Pageof 2