The combination of sulfurating agents with organoboranes is an underexploited synthetic transformation. The reactivity of borate complexes was investigated with several electrophilic sulfur species. Simple and practical methods for making carbon–sulfur bonds were created under almost neutral conditions. These enjoy a heavy metal-free environment and use not so toxic boron compounds. This is in contrast to the manipulation of poisonous H2S or the use of sulfur with Grignard reagents, under highly basic an
Organoborane compounds are among the most commonly employed intermediates in organic synthesis and s...
Organoboron reagents, especially boronic acids and boronates, have been widely explored as suitable ...
The development of a gold(I)-catalyzed sulfination of aryl boronic acids is described. This transfor...
Alkylboronates play an important role in synthetic chemistry, materials science and drug discovery. ...
International audienceThe radical chemistry based on organosulfur derivatives constitutes a powerful...
The first ring-forming thioboration reaction of C-C π bonds is reported. This catalyst-free method p...
Monochloroborane–dimethyl sulphide, BH2Cl.SMe2, is formed in essentially quantitative yield upon ref...
The reactivity of L<sub>2</sub>PhB: (<b>1</b>; L = oxazol-2-ylidene) as well as its transition-metal...
Organoborane compounds are highly used in a huge number of fields, from medicine, in the boron neutr...
A practical and direct method was developed for the production of versatile alkyl boronate esters vi...
Reported herein is a photochemical strategy for the borylation of alkyl halides using bis(catecholat...
Organoboranes are molecules that contain a carbon-boron bond. They play a pivotal role in organic sy...
A simple, regiocontrolled, and transition-metal-free approach to access exclusively 3-borylated thio...
Z-1-Iodo-1-hexen-1-ylpinacolboronate and two related compounds could be prepared by hydroboration of...
This article focuses on contemporary applications of boron complexes in organic synthesis—where the ...
Organoborane compounds are among the most commonly employed intermediates in organic synthesis and s...
Organoboron reagents, especially boronic acids and boronates, have been widely explored as suitable ...
The development of a gold(I)-catalyzed sulfination of aryl boronic acids is described. This transfor...
Alkylboronates play an important role in synthetic chemistry, materials science and drug discovery. ...
International audienceThe radical chemistry based on organosulfur derivatives constitutes a powerful...
The first ring-forming thioboration reaction of C-C π bonds is reported. This catalyst-free method p...
Monochloroborane–dimethyl sulphide, BH2Cl.SMe2, is formed in essentially quantitative yield upon ref...
The reactivity of L<sub>2</sub>PhB: (<b>1</b>; L = oxazol-2-ylidene) as well as its transition-metal...
Organoborane compounds are highly used in a huge number of fields, from medicine, in the boron neutr...
A practical and direct method was developed for the production of versatile alkyl boronate esters vi...
Reported herein is a photochemical strategy for the borylation of alkyl halides using bis(catecholat...
Organoboranes are molecules that contain a carbon-boron bond. They play a pivotal role in organic sy...
A simple, regiocontrolled, and transition-metal-free approach to access exclusively 3-borylated thio...
Z-1-Iodo-1-hexen-1-ylpinacolboronate and two related compounds could be prepared by hydroboration of...
This article focuses on contemporary applications of boron complexes in organic synthesis—where the ...
Organoborane compounds are among the most commonly employed intermediates in organic synthesis and s...
Organoboron reagents, especially boronic acids and boronates, have been widely explored as suitable ...
The development of a gold(I)-catalyzed sulfination of aryl boronic acids is described. This transfor...