This paper outlines the development of a protocol that allows in situ generation of unstable alkynes under Pd-catalyzed cross-coupling conditions. Cu-mediated intramolecular cyclization of the resultant α,ω-polyynes provides dehydrobenzoannulenes as singular species, in very good overall yields, and in a variety of topologies that are inaccessible by traditional routes or previously available in low yield only. In addition, we will discuss the solid-state structure and reactivity of these macrocycles, as well as the ability of the planar dehydrobenzoannulenes to support weak induced ring currents.
A direct one‐pot synthesis of asymmetric dehydrobenzopyrido[12]annulenes 2 and 3 containing one or t...
Annulenes possess properties that may play an important role in the development of electronic device...
The conceptual dehydrogenation of pericyclic reactions yields dehydropericyclic processes, which usu...
This paper outlines the development of a protocol that allows in situ generation of unstable alkynes...
Dehydrobenzoannulene derivatives containing isolated alkene linkages were synthesized by combining a...
Biaryl bonds are a common motif found in biologically active compounds and the majority of marketed ...
In this study, π-conjugated molecular wires strapped by cyclic π-conjugated side chains were efficie...
Pure hydrocarbons with shape and conjugation properties that can be switched by external stimuli is ...
A new polymerization route for the preparation of functional heterocyclic polymers was developed fro...
We report a computational and experimental study of the reaction of oxadiazinones and strained alkyn...
A straightforward methodology for the decarboxylative cross-coupling of aryl bromides and phenylprop...
Nanographenes (NGs) of unique shape, size and properties are always at the center of attraction beca...
Nanographenes (NGs) of unique shape, size and properties are always at the center of attraction beca...
Synthesis of Dehydrobenzoannulenes (DBAs) with pyrene core from 1,8-diethynylpyrene and 1,3,6,8-tetr...
The Lautens group has investigated the use of metal catalysts for the domino synthesis of heterocycl...
A direct one‐pot synthesis of asymmetric dehydrobenzopyrido[12]annulenes 2 and 3 containing one or t...
Annulenes possess properties that may play an important role in the development of electronic device...
The conceptual dehydrogenation of pericyclic reactions yields dehydropericyclic processes, which usu...
This paper outlines the development of a protocol that allows in situ generation of unstable alkynes...
Dehydrobenzoannulene derivatives containing isolated alkene linkages were synthesized by combining a...
Biaryl bonds are a common motif found in biologically active compounds and the majority of marketed ...
In this study, π-conjugated molecular wires strapped by cyclic π-conjugated side chains were efficie...
Pure hydrocarbons with shape and conjugation properties that can be switched by external stimuli is ...
A new polymerization route for the preparation of functional heterocyclic polymers was developed fro...
We report a computational and experimental study of the reaction of oxadiazinones and strained alkyn...
A straightforward methodology for the decarboxylative cross-coupling of aryl bromides and phenylprop...
Nanographenes (NGs) of unique shape, size and properties are always at the center of attraction beca...
Nanographenes (NGs) of unique shape, size and properties are always at the center of attraction beca...
Synthesis of Dehydrobenzoannulenes (DBAs) with pyrene core from 1,8-diethynylpyrene and 1,3,6,8-tetr...
The Lautens group has investigated the use of metal catalysts for the domino synthesis of heterocycl...
A direct one‐pot synthesis of asymmetric dehydrobenzopyrido[12]annulenes 2 and 3 containing one or t...
Annulenes possess properties that may play an important role in the development of electronic device...
The conceptual dehydrogenation of pericyclic reactions yields dehydropericyclic processes, which usu...