An operationally simple, efficient, and metal-/peroxide-free three-component reaction of alkynes, iodine, and sodium sulfinates has been developed for the construction of highly functionalized tetrasubstituted alkenes. Iodo- and sulfonyl-containing tetrasubstituted alkenes, such as vinyl ketones, allylic alcohols, and conjugated enynes, could be obtained regio- and stereoselectively in up to 96% yield
A novel metal-free strategy for a rapid and α-selctive C-alkynylation of glycals was developed. The ...
The synthesis of homopropargylic alcohols under metal-free and mild condition is described. This tra...
Recent efforts in designing expeditious catalytic synthesis of tetrasubstituted olefins have in part...
An operationally simple, efficient, and metal-/peroxide-free three-component reaction of alkynes, io...
A newly developed regio- and stereoselective radical addition of alkyne under metal-free conidtions ...
A metal-free CH–CH-type coupling of arenes and alkynes, mediated by a multifunctional sulfoxide dire...
A metal-free, open-flask protocol was developed for the preparation of allylic sulfones through dire...
A highly selective formation of geometrically defined acyclic tri- and tetrasubstituted alkenes from...
The first regioselective phenoxysulfonylation of alkynes with sodium sulfinate and phenol catalyzed ...
A method for the regio- and stereoselective synthesis of highly substituted vinyl ethers via trans-1...
<p>An efficient coupling reaction of allyl bromides with various alcohols as nucleophiles activated ...
An efficient method for the construction of Csp<sup>2</sup>–Csp<sup>3</sup> bond in a regio- and ste...
We report a one-pot, three-component synthesis of sulfides by exploiting a sulfoxide reagent as a fo...
A novel and practical method for the selenosulfonation of alkynes with the insertion of sulfur dioxi...
Iodine is found to be an efficient catalyst for the three-component coupling of aldehydes, alcohols,...
A novel metal-free strategy for a rapid and α-selctive C-alkynylation of glycals was developed. The ...
The synthesis of homopropargylic alcohols under metal-free and mild condition is described. This tra...
Recent efforts in designing expeditious catalytic synthesis of tetrasubstituted olefins have in part...
An operationally simple, efficient, and metal-/peroxide-free three-component reaction of alkynes, io...
A newly developed regio- and stereoselective radical addition of alkyne under metal-free conidtions ...
A metal-free CH–CH-type coupling of arenes and alkynes, mediated by a multifunctional sulfoxide dire...
A metal-free, open-flask protocol was developed for the preparation of allylic sulfones through dire...
A highly selective formation of geometrically defined acyclic tri- and tetrasubstituted alkenes from...
The first regioselective phenoxysulfonylation of alkynes with sodium sulfinate and phenol catalyzed ...
A method for the regio- and stereoselective synthesis of highly substituted vinyl ethers via trans-1...
<p>An efficient coupling reaction of allyl bromides with various alcohols as nucleophiles activated ...
An efficient method for the construction of Csp<sup>2</sup>–Csp<sup>3</sup> bond in a regio- and ste...
We report a one-pot, three-component synthesis of sulfides by exploiting a sulfoxide reagent as a fo...
A novel and practical method for the selenosulfonation of alkynes with the insertion of sulfur dioxi...
Iodine is found to be an efficient catalyst for the three-component coupling of aldehydes, alcohols,...
A novel metal-free strategy for a rapid and α-selctive C-alkynylation of glycals was developed. The ...
The synthesis of homopropargylic alcohols under metal-free and mild condition is described. This tra...
Recent efforts in designing expeditious catalytic synthesis of tetrasubstituted olefins have in part...