Arylboron compounds are widely available and synthetically useful reagents in which the boron group is typically substituted. Herein, we show that the boron group and -hydrogen atom are substituted in a formal cycloaddition reaction. This transformation is enabled by a one-pot sequence involving diaryliodonium and aryne intermediates. The scope of arylboron reagents and arynophiles is demonstrated, and the method is applied to the formal synthesis of an investigational drug candidate
&strad- Using two synthetic methods, flash vacuum pyrolyses (fvp) and met-al supported cyclizati...
Arynes were generated in situ from ortho-silyl aryl triflates and fluoride ions in the presence of s...
A transition-metal-free method for the synthesis of benzylic boronate esters with arylboronic acids ...
A regio- and chemoselective C-H deprotonative strategy toward arynes is described that employs a hyp...
Heteroatom incorporation is a general strategy for modulating the electronic properties of organic s...
This review covers the application of cycloaddition reactions in forming the boron-containing compou...
Among the numerous routes organic chemists have developed to synthesize benzene derivatives and hete...
This thesis concerns the development of metal-free reactions to obtain carbon-heteroatom and carbon-...
Pd-catalyzed cyclization of 1,6-enynes in the presence of bis(pinacolato)diboron affords homoallylic...
Among the numerous routes organic chemists have developed to synthesize benzene derivatives and hete...
Arynes offer immense potential for diversification of benzenoid rings, which occur in pharmaceutical...
This thesis concerns the development of metal-free reactions to obtain carbon-heteroatom and carbon-...
A transition-metal-free method for the synthesis of benzylic boronate esters with arylboronic acids ...
We report a synthetic platform for the formation of benzylic C–X bonds. Benzylboronic acid pinacol (...
Arynes were generated in situ from ortho-silyl aryl triflates and fluoride ions in the presence of s...
&strad- Using two synthetic methods, flash vacuum pyrolyses (fvp) and met-al supported cyclizati...
Arynes were generated in situ from ortho-silyl aryl triflates and fluoride ions in the presence of s...
A transition-metal-free method for the synthesis of benzylic boronate esters with arylboronic acids ...
A regio- and chemoselective C-H deprotonative strategy toward arynes is described that employs a hyp...
Heteroatom incorporation is a general strategy for modulating the electronic properties of organic s...
This review covers the application of cycloaddition reactions in forming the boron-containing compou...
Among the numerous routes organic chemists have developed to synthesize benzene derivatives and hete...
This thesis concerns the development of metal-free reactions to obtain carbon-heteroatom and carbon-...
Pd-catalyzed cyclization of 1,6-enynes in the presence of bis(pinacolato)diboron affords homoallylic...
Among the numerous routes organic chemists have developed to synthesize benzene derivatives and hete...
Arynes offer immense potential for diversification of benzenoid rings, which occur in pharmaceutical...
This thesis concerns the development of metal-free reactions to obtain carbon-heteroatom and carbon-...
A transition-metal-free method for the synthesis of benzylic boronate esters with arylboronic acids ...
We report a synthetic platform for the formation of benzylic C–X bonds. Benzylboronic acid pinacol (...
Arynes were generated in situ from ortho-silyl aryl triflates and fluoride ions in the presence of s...
&strad- Using two synthetic methods, flash vacuum pyrolyses (fvp) and met-al supported cyclizati...
Arynes were generated in situ from ortho-silyl aryl triflates and fluoride ions in the presence of s...
A transition-metal-free method for the synthesis of benzylic boronate esters with arylboronic acids ...