Selective lithiation of bis(azol-1-yl)methanes
- 1 January 1993
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 9,p. 1079-1083
- https://doi.org/10.1039/p19930001079
Abstract
Lithiation of bis(azol-1-yl)methanes and subsequent reaction with electrophiles yields selectively monoand di-ring-substituted derivatives. The regioselectivity observed is explained in terms of the structure of the substrate, the hard and soft acids and bases principle, and the nature of the electrophile used.Keywords
This publication has 5 references indexed in Scilit:
- Lithiation of 1-benzylimidazole. A hypothesis on the regioselectivity of the electrophilic attacks on the lithiated speciesJournal of Heterocyclic Chemistry, 1990
- Triazole phosphonates. Electrophilic substitution of 1‐substituted‐1H‐1,2,4‐triazoles via lithiated triazole intermediatesJournal of Heterocyclic Chemistry, 1986
- The Coordination Chemistry of Pyrazole‐Derived LigandsPublished by Wiley ,1986
- Rhodium(I) complexes with bis(pyrazolyl)methane ligands. Crystal structure of [Rh(COD)(CH2(Pz)2)]ClO4· C2H4Cl2Journal of Organometallic Chemistry, 1984
- The lithiation of gem-bis (pyrazol-1-yl)alkanesTetrahedron, 1983