Directed lithiation of substituted aromatics and heterocycles containing a directing metalating group with alkyllithium in anhydrous tetrahydrofuran or diethyl ether at low temperature provides the corresponding lithium intermediates. Reaction of the lithium reagents obtained in situ with various electrophiles gives the corresponding substituted derivatives in high yields. The process has been applied for various derivatives and has proven to be a convenient method for modification of ring systems. This brief review highlights the importance of directing metalating groups in directed lithiation of simple aromatic compounds and some common heterocycles as a tool for regioselective substitution
Benzenethiol, toluene-4-thio1, and 3,5-dimethylbenzenethiol are doubly lithiated (on sulfur and on c...
The use of diethyl ether–tetrahydrofuran–light petroleum (b.p. 30–40 °C)(4:3:1) as solvent for the r...
Lithiation of 3-methylthiophene with lithium 2,2,6,6-tetra-methylpiperidide (LiTMP) is highly select...
Directed lithiation of substituted aromatics and heterocycles containing a directing metalating grou...
Directed lithiation of substituted pyridines containing a directing metalating group (DMG) with a li...
This review deals with directed and regioselective lithiation of various quinazoline derivatives by ...
Part 1: A widely used method of preparing organolithium compounds is by the reductive lithiation of ...
Lithiation of N′-phenethyl-N,N-dimethylurea with three equivalents of tert-butyllithium in anhydrous...
Regioselectivity is an important aspect in the design of organic protocols involving Directed ortho-...
Directed lithiation of various substituted benzylamines takes different courses depending on the sub...
Lithiation of various N′-aryl-N,N-dimethylureas takes different courses depending on the substituent...
Benzenethiol, toluene-4-thio1, and 3,5-dimethylbenzenethiol are doubly lithiated (on sulfur and on c...
The use of diethyl ether–tetrahydrofuran–light petroleum (b.p. 30–40 °C)(4:3:1) as solvent for the r...
Lithiation of 3-methylthiophene with lithium 2,2,6,6-tetra-methylpiperidide (LiTMP) is highly select...
Directed lithiation of substituted aromatics and heterocycles containing a directing metalating grou...
Directed lithiation of substituted pyridines containing a directing metalating group (DMG) with a li...
This review deals with directed and regioselective lithiation of various quinazoline derivatives by ...
Part 1: A widely used method of preparing organolithium compounds is by the reductive lithiation of ...
Lithiation of N′-phenethyl-N,N-dimethylurea with three equivalents of tert-butyllithium in anhydrous...
Regioselectivity is an important aspect in the design of organic protocols involving Directed ortho-...
Directed lithiation of various substituted benzylamines takes different courses depending on the sub...
Lithiation of various N′-aryl-N,N-dimethylureas takes different courses depending on the substituent...
Benzenethiol, toluene-4-thio1, and 3,5-dimethylbenzenethiol are doubly lithiated (on sulfur and on c...
The use of diethyl ether–tetrahydrofuran–light petroleum (b.p. 30–40 °C)(4:3:1) as solvent for the r...
Lithiation of 3-methylthiophene with lithium 2,2,6,6-tetra-methylpiperidide (LiTMP) is highly select...