Highly strained unsaturated carbocyclic rings are high-energy compounds which are attracting increasing interest \u2013 not just for their peculiar structural and reactivity features \u2013 but also as modern chemical tools for bioorthogonal and in vivo chemistry, especially via inverse-electron demand Diels\u2013Alder (iEDDA) and strain-promoted azide-alkyne cycloaddition (SPAAC) reactions. This mini-review covers two main classes of compounds: 3 to 10 membered-ring cycloalkynes and trans-cycloalkenes, including some examples of cyclic enynes, dienes and bridgehead alkenes. Their molecular properties, synthesis and reactivity are presented and discussed, with an emphasis on their functionalization and reactivity
The development of efficient methods for constructing carbocycles continues to be an important goal ...
The Diels–Alder reactivities of a series of cycloalkenes, from the highly strained cyclopropene to t...
We report a computational and experimental study of the reaction of oxadiazinones and strained alkyn...
A new class of macrocyclic angle-strained alkynes whose size and reactivity can be precisely tuned b...
A nearly forgotten reaction discovered more than 60 years ago—the cycloaddition of a cyclic alkyne a...
The Diels-Alder reactivities of a series of cycloalkenes, from the highly strained cyclopropene to t...
The factors controlling the reactivity of the strained-alkyne embedded cycloparaphenylenes have been...
The Diels-Alder reactions of the cycloalkenes, cyclohexene through cyclopropene, with a series of di...
Strained cycloalkynes are of considerable interest to theoreticians and experimentalists, and posses...
Abstract- Several strained ring and electronically activated hydrocarbons have been synthesized via ...
Bioorthogonal chemistry has had a major impact on the study of biological processes in vivo. Biomole...
Improving the synthesis of complex organic molecules is essential for progress in many fields such a...
A series of strained alkynes, based on the 2,2’-dihydroxy-1,1’-biaryl structure, were prepared in a ...
The Diels–Alder reactions of the cycloalkenes, cyclohexene through cyclopropene, with a series of di...
A concise, practical and stereoselective entry into macrocyclic (E)-alkenes is outlined comprising a...
The development of efficient methods for constructing carbocycles continues to be an important goal ...
The Diels–Alder reactivities of a series of cycloalkenes, from the highly strained cyclopropene to t...
We report a computational and experimental study of the reaction of oxadiazinones and strained alkyn...
A new class of macrocyclic angle-strained alkynes whose size and reactivity can be precisely tuned b...
A nearly forgotten reaction discovered more than 60 years ago—the cycloaddition of a cyclic alkyne a...
The Diels-Alder reactivities of a series of cycloalkenes, from the highly strained cyclopropene to t...
The factors controlling the reactivity of the strained-alkyne embedded cycloparaphenylenes have been...
The Diels-Alder reactions of the cycloalkenes, cyclohexene through cyclopropene, with a series of di...
Strained cycloalkynes are of considerable interest to theoreticians and experimentalists, and posses...
Abstract- Several strained ring and electronically activated hydrocarbons have been synthesized via ...
Bioorthogonal chemistry has had a major impact on the study of biological processes in vivo. Biomole...
Improving the synthesis of complex organic molecules is essential for progress in many fields such a...
A series of strained alkynes, based on the 2,2’-dihydroxy-1,1’-biaryl structure, were prepared in a ...
The Diels–Alder reactions of the cycloalkenes, cyclohexene through cyclopropene, with a series of di...
A concise, practical and stereoselective entry into macrocyclic (E)-alkenes is outlined comprising a...
The development of efficient methods for constructing carbocycles continues to be an important goal ...
The Diels–Alder reactivities of a series of cycloalkenes, from the highly strained cyclopropene to t...
We report a computational and experimental study of the reaction of oxadiazinones and strained alkyn...