Preparation and Reactivity of Organometallic Reagents Leading to Functionalized N -Heteroaromatics
Abstract
Main-group organometallic reagents played a pivotal role in organic synthesis, with numerous applications, ranging from pharmaceutical industries to material science. Especially, functionalized heterocyclic molecules may be prepared using main-group organometallics and have multiple applications due to their electronic and chemical properties. This comprehensive review emphasized the significance of functionalized organo-Li, -Mg, -Zn, -Al, -Mn, -Cu, -B, -Na, -La, -In, -Cd, and -Zr reagents for the selective functionalization of N -heteroaromatic scaffolds. Our major focus was on advanced synthetic methods for the preparation of densely functionalized N -heteroaromatic compounds. In recent years, various leading research groups developed highly reactive, air- and moisture-stable organometallic reagents that permitted a broad range of cross-coupling reactions (C–C, C–N, C–S, and C–X) using various electrophiles. We will describe the various preparations of N -heteroromatic organometallics (direct metal insertions, halogen–metal exchanges, transmetalations or directed metalations), showing the advantages and limitations of each method. Moreover, the use of low-cost and less toxic transition-metal-catalyzed processes with air-stable zinc reagents or TMP bases under sustainable conditions, offered alternative synthetic pathways for the preparation of fused N -heteroaromatic-based natural products and drugs. In this context, this review article points to new approaches for the functionalization of N -heteroaromatic scaffolds using various main-group organometallic reagents published between 2010 and 2024.
Fields of Study & Subjects
Coordination Chemistry and Organometallics
Catalytic Cross-Coupling Reactions
Catalytic C–H Functionalization Methods
Publication details
- Journal / source
- Chemical Reviews
- Publisher
- American Chemical Society (ACS)
- Volume
- 126
- Issue
- 4
- Pages
- 2582–2652
- Publication date
- 5 February 2026
- Language
- EN