A strain-release-driven, cation-templated nucleophilic 7- and 8-exo-trig-cyclization of tethered Boc-protected amines to cyclopropenes is described. The featured reaction proceeds in diastereo- and regioselective fashion and allows for preparation of the corresponding 2,5-diazabicyclo[5.1.0]octan-6-ones and 2,6-diazabicyclo[6.1.0]nonan-7-ones as sole products in high yields. Preliminary studies on anticancer activities of these novel cyclopropane-fused medium heterocycles were performed
A strain-release-driven, cation-templated intramolecular nucleophilic addition of tethered alkoxides...
This thesis is concerned with the development of methods by which to access compounds possessing the...
This thesis is concerned with the development of methods by which to access compounds possessing the...
A strain-release-driven, cation-templated nucleophilic 7- and 8-exo-trig-cyclization of tethered Boc...
A strain-release-driven, cation-templated nucleophilic 7- and 8-exo-trig-cyclization of tethered Boc...
A strain-release-driven, cation-templated nucleophilic 7- and 8-exo-trig-cyclization of tethered Boc...
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ...
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ...
The sulfonamide moiety was evaluated as an activating and stabilizing functional group in the metal-...
The sulfonamide moiety was evaluated as an activating and stabilizing functional group in the metal-...
The sulfonamide moiety was evaluated as an activating and stabilizing functional group in the metal-...
This thesis is focused on the development and application of methods for the intramolecular nucleoph...
This thesis is focused on the development and application of methods for the intramolecular nucleoph...
A strain-release-driven, cation-templated intramolecular nucleophilic addition of tethered alkoxides...
A strain-release-driven, cation-templated intramolecular nucleophilic addition of tethered alkoxides...
A strain-release-driven, cation-templated intramolecular nucleophilic addition of tethered alkoxides...
This thesis is concerned with the development of methods by which to access compounds possessing the...
This thesis is concerned with the development of methods by which to access compounds possessing the...
A strain-release-driven, cation-templated nucleophilic 7- and 8-exo-trig-cyclization of tethered Boc...
A strain-release-driven, cation-templated nucleophilic 7- and 8-exo-trig-cyclization of tethered Boc...
A strain-release-driven, cation-templated nucleophilic 7- and 8-exo-trig-cyclization of tethered Boc...
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ...
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ...
The sulfonamide moiety was evaluated as an activating and stabilizing functional group in the metal-...
The sulfonamide moiety was evaluated as an activating and stabilizing functional group in the metal-...
The sulfonamide moiety was evaluated as an activating and stabilizing functional group in the metal-...
This thesis is focused on the development and application of methods for the intramolecular nucleoph...
This thesis is focused on the development and application of methods for the intramolecular nucleoph...
A strain-release-driven, cation-templated intramolecular nucleophilic addition of tethered alkoxides...
A strain-release-driven, cation-templated intramolecular nucleophilic addition of tethered alkoxides...
A strain-release-driven, cation-templated intramolecular nucleophilic addition of tethered alkoxides...
This thesis is concerned with the development of methods by which to access compounds possessing the...
This thesis is concerned with the development of methods by which to access compounds possessing the...