This document is the Accepted Manuscript version of a Published Work that appeared in final form in The Journal of Organic 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/acs.joc.8b02062.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...
Copyright © ARKAT USA, Inc The document attached has been archived with permission from the publishe...
Over the past decades, functional group manipulation of aromatic precursors has been a common strate...
Supramolecular chemistry involves the formation of complex molecular entities that have the capacity...
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ...
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 thesis is focused on the development and application of methods for the intramolecular nucleoph...
This thesis is concerned with the development of methods by which to access compounds possessing the...
© 2015 Elsevier Ltd. All rights reserved. Functionalised azepane and oxepane scaffolds were prepared...
Cyclopropanations of an 8-oxabicyclo[3.2.1]octene substrate using diazocarbonyl compounds provided e...
La cycloaddition dipolaire 1,3-du 2-diazopropane 1 et des arylnitriloxydes 7a-c sur les cinnamoyl cy...
The cyclopropane containing betaine, rac-dysibetaine CPa, was prepared from (1-methoxycarbonylpentad...
1,3-Dipolar cycloaddition reactions involving 2-diazopropane (DAP) 1 and pyrones 2a,b or activated c...
Unique examples of aza-Heck-based C(sp3)-H functionalization cascades are described. Under Pd(0)-cat...
Amino alcohols, cyclopropanes and nitriles are privileged structural motifs found in the scaffold of...
Copyright © ARKAT USA, Inc The document attached has been archived with permission from the publishe...
Over the past decades, functional group manipulation of aromatic precursors has been a common strate...
Supramolecular chemistry involves the formation of complex molecular entities that have the capacity...
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ...
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 thesis is focused on the development and application of methods for the intramolecular nucleoph...
This thesis is concerned with the development of methods by which to access compounds possessing the...
© 2015 Elsevier Ltd. All rights reserved. Functionalised azepane and oxepane scaffolds were prepared...
Cyclopropanations of an 8-oxabicyclo[3.2.1]octene substrate using diazocarbonyl compounds provided e...
La cycloaddition dipolaire 1,3-du 2-diazopropane 1 et des arylnitriloxydes 7a-c sur les cinnamoyl cy...
The cyclopropane containing betaine, rac-dysibetaine CPa, was prepared from (1-methoxycarbonylpentad...
1,3-Dipolar cycloaddition reactions involving 2-diazopropane (DAP) 1 and pyrones 2a,b or activated c...
Unique examples of aza-Heck-based C(sp3)-H functionalization cascades are described. Under Pd(0)-cat...
Amino alcohols, cyclopropanes and nitriles are privileged structural motifs found in the scaffold of...
Copyright © ARKAT USA, Inc The document attached has been archived with permission from the publishe...
Over the past decades, functional group manipulation of aromatic precursors has been a common strate...
Supramolecular chemistry involves the formation of complex molecular entities that have the capacity...