A newly developed regio- and stereoselective radical addition of alkyne under metal-free conidtions has been disclosed. This chemistry, in which odorless sodium arenesulfinates in place of thiols are used as the sulfur reagent, provides an efficient, one-pot approach for the generation of β-iodoalkenyl sulfides, which can be easily further functionalized to derive various alkenes and alkynyl sulfides rendering this methodology attractive to both synthetic and medicinal chemistry
A mild, efficient and straightforward visible-light-driven method has been developed to construct 1,...
The presence of sulfur in numerous blockbuster drugs, natural products and other medicinally active ...
A practical and novel approach has been developed for the synthesis of vinyl sulfides by the reactio...
An operationally simple, efficient, and metal-/peroxide-free three-component reaction of alkynes, io...
ABSTRACT: Among all functional groups, alkynes occupy a privileged position in synthetic and medicin...
A visible-light organophotoredox-catalyzed sulfurization of alkenes and alkynes with aromatic and he...
<div><p></p><p>An atom-economical and environmentally friendly method for synthesis of bromo-substit...
An iodine-promoted one-pot radical cyclization reaction of 1,6-enynes with sulfonyl hydrazides to pr...
A new protocol for the one-pot synthesis of styryl alkyl sulfides was developed. This methodology in...
A novel and practical method for the selenosulfonation of alkynes with the insertion of sulfur dioxi...
Herein, a one-step chlorosulfonylation of alkynes via a photocatalytic redox process is described. A...
The first regioselective phenoxysulfonylation of alkynes with sodium sulfinate and phenol catalyzed ...
As an indispensable part of click chemistry, thiol-yne reactions are of great importance in organic ...
We report a one-pot, three-component synthesis of sulfides by exploiting a sulfoxide reagent as a fo...
A simple, efficient, and practical metal-free C–H sulfenylation of substituted electron-rich arenes ...
A mild, efficient and straightforward visible-light-driven method has been developed to construct 1,...
The presence of sulfur in numerous blockbuster drugs, natural products and other medicinally active ...
A practical and novel approach has been developed for the synthesis of vinyl sulfides by the reactio...
An operationally simple, efficient, and metal-/peroxide-free three-component reaction of alkynes, io...
ABSTRACT: Among all functional groups, alkynes occupy a privileged position in synthetic and medicin...
A visible-light organophotoredox-catalyzed sulfurization of alkenes and alkynes with aromatic and he...
<div><p></p><p>An atom-economical and environmentally friendly method for synthesis of bromo-substit...
An iodine-promoted one-pot radical cyclization reaction of 1,6-enynes with sulfonyl hydrazides to pr...
A new protocol for the one-pot synthesis of styryl alkyl sulfides was developed. This methodology in...
A novel and practical method for the selenosulfonation of alkynes with the insertion of sulfur dioxi...
Herein, a one-step chlorosulfonylation of alkynes via a photocatalytic redox process is described. A...
The first regioselective phenoxysulfonylation of alkynes with sodium sulfinate and phenol catalyzed ...
As an indispensable part of click chemistry, thiol-yne reactions are of great importance in organic ...
We report a one-pot, three-component synthesis of sulfides by exploiting a sulfoxide reagent as a fo...
A simple, efficient, and practical metal-free C–H sulfenylation of substituted electron-rich arenes ...
A mild, efficient and straightforward visible-light-driven method has been developed to construct 1,...
The presence of sulfur in numerous blockbuster drugs, natural products and other medicinally active ...
A practical and novel approach has been developed for the synthesis of vinyl sulfides by the reactio...