7A protection-deprotection strategy for strained alkynes used for bioorthogonal chemistry is reported. A strained alkyne can be protected with dicobalt-octacarbonyl and we demonstrate for the first time that a strained alkyne can be re-formed and isolated under mild reaction conditions for further bioorthogonal reactivity. The protection-deprotection strategy herein reported will expand the versatility of strained alkynes for the preparation of substrates in chemical biology and materials applications.nonenoneGobbo P; Romagnoli T; Barbon SM; Price JT; Keir J; Gilroy JB; Workentin MSGobbo, P; Romagnoli, T; Barbon, Sm; Price, Jt; Keir, J; Gilroy, Jb; Workentin, M
Protein sulfenic acids are formed by the reaction of biologically relevant reactive oxygen species w...
Thiolate anions have been generated in a "demand-based" fashion under virtually neutral conditions f...
Quantum mechanical calculations have been used to study the intramolecular additions of hydroxylamin...
Strained alkynes, i.e., alkynes distorted from the ideal linear geometry, undergo cycloaddition reac...
A series of strained alkynes were prepared from 2,2′-dihydroxy-biaryls. Several were characterised b...
A series of strained alkynes, based on the 2,2’-dihydroxy-1,1’-biaryl structure, were prepared in a ...
The novel “double strained alkyne” 3 has been prepared and evaluated in strain-promoted azide-alkyne...
We report a mild method for the selective deprotection of the N-Boc group from a structurally divers...
Abstract. Several conditions to deprotect triisopropylsilylarylacetylenes were examined. The triisop...
Versatile water- and organic solvent-soluble AuNPs that incorporate an interfacial strained alkyne c...
A nearly forgotten reaction discovered more than 60 years ago—the cycloaddition of a cyclic alkyne a...
The factors controlling the reactivity of the strained-alkyne embedded cycloparaphenylenes have been...
A competent and fast method for the deprotection of trimethyl silyl group was attained by using chea...
Abstract- Several strained ring and electronically activated hydrocarbons have been synthesized via ...
The Sondheimer dialkyne is extensively used in double strain-promoted azide-alkyne cycloadditions. T...
Protein sulfenic acids are formed by the reaction of biologically relevant reactive oxygen species w...
Thiolate anions have been generated in a "demand-based" fashion under virtually neutral conditions f...
Quantum mechanical calculations have been used to study the intramolecular additions of hydroxylamin...
Strained alkynes, i.e., alkynes distorted from the ideal linear geometry, undergo cycloaddition reac...
A series of strained alkynes were prepared from 2,2′-dihydroxy-biaryls. Several were characterised b...
A series of strained alkynes, based on the 2,2’-dihydroxy-1,1’-biaryl structure, were prepared in a ...
The novel “double strained alkyne” 3 has been prepared and evaluated in strain-promoted azide-alkyne...
We report a mild method for the selective deprotection of the N-Boc group from a structurally divers...
Abstract. Several conditions to deprotect triisopropylsilylarylacetylenes were examined. The triisop...
Versatile water- and organic solvent-soluble AuNPs that incorporate an interfacial strained alkyne c...
A nearly forgotten reaction discovered more than 60 years ago—the cycloaddition of a cyclic alkyne a...
The factors controlling the reactivity of the strained-alkyne embedded cycloparaphenylenes have been...
A competent and fast method for the deprotection of trimethyl silyl group was attained by using chea...
Abstract- Several strained ring and electronically activated hydrocarbons have been synthesized via ...
The Sondheimer dialkyne is extensively used in double strain-promoted azide-alkyne cycloadditions. T...
Protein sulfenic acids are formed by the reaction of biologically relevant reactive oxygen species w...
Thiolate anions have been generated in a "demand-based" fashion under virtually neutral conditions f...
Quantum mechanical calculations have been used to study the intramolecular additions of hydroxylamin...