This document is the Accepted Manuscript version of a Published Work that appeared in final form in Journal of Combinatorial Chemistry, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://doi.org/10.1021/cc1001023.The construction of a library of benzothiaoxazepine-1,1’-dioxides utilizing a one-pot, SNAr diversification – ODCT50 scavenging protocol is reported. This protocol combines microwave irradiation to facilitate the reaction, in conjunction with a soluble ROMP-derived scavenger (ODCT) to afford the desired products in good overall purity. Utilizing this protocol, a 78-member library was successfully synthesized and submitted for biolo...
A microwave-assisted, sequential, one-pot protocol has been developed for the synthesis of a variety...
Privileged scaffolds which can unveil unknown territories of the chemical space are constantly promi...
A formal [4+3] epoxide cascade protocol utilizing ambiphilic sulfonamides and a variety of epoxides ...
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ...
The efficient synthesis of an 80-member library of unique benzoxathiazocine 1,1-dioxides by a microw...
The generation of stereochemically-rich benzothiaoxazepine-1,1′-dioxides for enrichment of high-thro...
This is the peer reviewed version of the following article: Ullah, F., Samarakoon, T., Rolfe, A., Ku...
The synthesis of a library of bicyclic sultams incorporating the 1,5,2-dithiazepine 1,1-dioxide moie...
The overarching goal of this dissertation is the development of strategies and methodologies aimed a...
A novel one-pot sulfonylation/intramolecular thia-Michael protocol is reported for the synthesis of ...
An atom-economical purification protocol, using solution phase processing via ring-opening metathesi...
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ...
A reaction pairing strategy centered on utilization of a reaction triad (sulfonylation, SNAr additio...
The development of methods to produce diverse set of small molecules to be utilized as chemical prob...
A microwave-assisted, sequential, one-pot protocol has been developed for the synthesis of a variety...
Privileged scaffolds which can unveil unknown territories of the chemical space are constantly promi...
A formal [4+3] epoxide cascade protocol utilizing ambiphilic sulfonamides and a variety of epoxides ...
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ...
The efficient synthesis of an 80-member library of unique benzoxathiazocine 1,1-dioxides by a microw...
The generation of stereochemically-rich benzothiaoxazepine-1,1′-dioxides for enrichment of high-thro...
This is the peer reviewed version of the following article: Ullah, F., Samarakoon, T., Rolfe, A., Ku...
The synthesis of a library of bicyclic sultams incorporating the 1,5,2-dithiazepine 1,1-dioxide moie...
The overarching goal of this dissertation is the development of strategies and methodologies aimed a...
A novel one-pot sulfonylation/intramolecular thia-Michael protocol is reported for the synthesis of ...
An atom-economical purification protocol, using solution phase processing via ring-opening metathesi...
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ...
A reaction pairing strategy centered on utilization of a reaction triad (sulfonylation, SNAr additio...
The development of methods to produce diverse set of small molecules to be utilized as chemical prob...
A microwave-assisted, sequential, one-pot protocol has been developed for the synthesis of a variety...
Privileged scaffolds which can unveil unknown territories of the chemical space are constantly promi...
A formal [4+3] epoxide cascade protocol utilizing ambiphilic sulfonamides and a variety of epoxides ...