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Ramesh Jasti

Showing results (11-20 of 73) with videos related to

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Organic Letters|November 5, 2011
Theoretical analysis of [5.7](n)cyclacenes: closed-shell cyclacene isomersElizabeth S Hirst, Feng Wang, Ramesh Jasti
Journal of the American Chemical Society|November 7, 2015
A Circle Has No End: Role of Cyclic Topology and Accompanying Structural Reorganization on the Hole Distribution in Cyclic and Linear Poly-p-phenylene Molecular WiresMarat R Talipov, Ramesh Jasti, Rajendra Rathore
Angewandte Chemie (International Ed. in English)|April 5, 2017
A Molecular Propeller with Three Nanohoop Blades: Synthesis, Characterization, and Solid-State PackingPenghao Li, Lev N Zakharov, Ramesh Jasti
Journal of the American Chemical Society|August 12, 2004
Axial-selective prins cyclizations by solvolysis of alpha-bromo ethersRamesh Jasti, Justin Vitale, Scott D Rychnovsky
The Journal of Organic Chemistry|July 19, 2012
Selective syntheses of [7]-[12]cycloparaphenylenes using orthogonal Suzuki-Miyaura cross-coupling reactionsEvan R Darzi, Thomas J Sisto, Ramesh Jasti
Angewandte Chemie (International Ed. in English)|June 10, 2020
Synthesis, Characterization, and Computational Investigation of Bright Orange-Emitting Benzothiadiazole [10]CycloparaphenyleneTerri C Lovell, Zachary R Garrison, Ramesh Jasti
Journal of the American Chemical Society|July 7, 2005
Utilization of an oxonia-Cope rearrangement as a mechanistic probe for Prins cyclizationsRamesh Jasti, Christopher D Anderson, Scott D Rychnovsky
Nature Chemistry|April 24, 2014
Efficient room-temperature synthesis of a highly strained carbon nanohoop fragment of buckminsterfullerenePaul J Evans, Evan R Darzi, Ramesh Jasti
Chemical Science|June 14, 2021
Strain visualization for strained macrocyclesCurtis E Colwell, Tavis W Price, Tim Stauch, et al.
Journal of the American Chemical Society|December 6, 2008
Synthesis, characterization, and theory of [9]-, [12]-, and [18]cycloparaphenylene: carbon nanohoop structuresRamesh Jasti, Joydeep Bhattacharjee, Jeffrey B Neaton, et al.
Pageof 8

Showing results (11-20 of 73) with videos related to

Sort By:
Pageof 8
Organic Letters|November 5, 2011
Theoretical analysis of [5.7](n)cyclacenes: closed-shell cyclacene isomersElizabeth S Hirst, Feng Wang, Ramesh Jasti
Journal of the American Chemical Society|November 7, 2015
A Circle Has No End: Role of Cyclic Topology and Accompanying Structural Reorganization on the Hole Distribution in Cyclic and Linear Poly-p-phenylene Molecular WiresMarat R Talipov, Ramesh Jasti, Rajendra Rathore
Angewandte Chemie (International Ed. in English)|April 5, 2017
A Molecular Propeller with Three Nanohoop Blades: Synthesis, Characterization, and Solid-State PackingPenghao Li, Lev N Zakharov, Ramesh Jasti
Journal of the American Chemical Society|August 12, 2004
Axial-selective prins cyclizations by solvolysis of alpha-bromo ethersRamesh Jasti, Justin Vitale, Scott D Rychnovsky
The Journal of Organic Chemistry|July 19, 2012
Selective syntheses of [7]-[12]cycloparaphenylenes using orthogonal Suzuki-Miyaura cross-coupling reactionsEvan R Darzi, Thomas J Sisto, Ramesh Jasti
Angewandte Chemie (International Ed. in English)|June 10, 2020
Synthesis, Characterization, and Computational Investigation of Bright Orange-Emitting Benzothiadiazole [10]CycloparaphenyleneTerri C Lovell, Zachary R Garrison, Ramesh Jasti
Journal of the American Chemical Society|July 7, 2005
Utilization of an oxonia-Cope rearrangement as a mechanistic probe for Prins cyclizationsRamesh Jasti, Christopher D Anderson, Scott D Rychnovsky
Nature Chemistry|April 24, 2014
Efficient room-temperature synthesis of a highly strained carbon nanohoop fragment of buckminsterfullerenePaul J Evans, Evan R Darzi, Ramesh Jasti
Chemical Science|June 14, 2021
Strain visualization for strained macrocyclesCurtis E Colwell, Tavis W Price, Tim Stauch, et al.
Journal of the American Chemical Society|December 6, 2008
Synthesis, characterization, and theory of [9]-, [12]-, and [18]cycloparaphenylene: carbon nanohoop structuresRamesh Jasti, Joydeep Bhattacharjee, Jeffrey B Neaton, et al.
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