Boron-Wittig olefination with gem-bis(boryl)alkanes

The condensation of easy manageable lithium alpha-bis(boryl)carbanions with carbonyl derivatives, the so-called boron-Wittig reaction, allows for the straightforward and often stereoselective formation of synthetically highly versatile metalloid-substituted alkenes, which are key building blocks on route to all-carbon substituted olefins. In this Tutorial review the concept behind this olefination reaction and its application to ketones, aldehydes and other carbonyl derivatives, such amides, ester and carboxylic acids, are presented in a systematic manner. A special emphasis has been placed on parameters controlling the stereochemical outcome of these transformations. To illustrate the great synthetic potential of this new methodological tool, a section is also included covering a selection of applications of the boron-Wittig reaction to target compounds via subsequent C-C bond-forming process.

Automated summary

The boron-Wittig reaction involves the condensation of easy manageable lithium alpha-bis(boryl)carbanions with carbonyl derivatives to form metalloid-substituted alkenes, which are important building blocks for the synthesis of all-carbon substituted olefins. This reaction is stereoselective and can be applied to a variety of carbonyl derivatives, with a focus on controlling the stereochemical outcome. Its synthetic potential is demonstrated through applications to target compounds via subsequent C-C bond forming processes.