After a long adolescence, the chemistry of lithium carbenoids has currently been entering its maturity bringing a dowry of a more in-depth and less empirical knowledge of the structure and configurational stability of such double-faced intermediates; this, thanks in particular to the synergistic and harmonic cooperation between calculations and the most modern NMR techniques now at our disposal. Such a knowledge has stimulated the development of fruitful stereoselective applications in the field of organic synthesis providing as well a rationale to observed selectivities. Such aspects together with the role played by aggregation and solvation on the structure-reactivity relationship have been highlighted throughout this Minireview with sele...
The effects of lithium alkoxides on the rates of reactions and on the structures of a series of tert...
265 p.Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1997.A series of tin-lithium excha...
Attempts to generate the free bis(N-heterocyclic carbene) vegi<sup>R</sup> (R = <i>n</i>Pr, <i>t</i...
This chapter addresses the reactivity of a-lithiated organohalogens, ethers, and amines. Special emp...
Computational quantum chemistry was used to investigate the structures of lithium carbamates in the ...
Electronic stabilization of the negative charge by a thiophosphinoyl and pyridyl/quinolyl substituen...
The role of O-Lithiated species has a very strong precedence in literature ranging from well-known r...
Computational results are presented to support experimental evidence that cyclopropanation reactions...
Progress toward understanding the reactivity of synthetically important lithium enolates relies on t...
Abstract- The dimerization energies of lithium compounds, 2LiX-(LiX)9, are quite large and depend pr...
The method of continuous variation (MCV) was used in conjunction with <sup>6</sup>Li NMR spectroscop...
Waerder B, Steinhauer S, Neumann B, et al. Solid-State Structure of a Li/F Carbenoid: Pentafluoroeth...
s-Block metal carbenoids are carbene synthons and applied in a myriad of organic transformations. Th...
A multifaceted approach to the study of the structure and reactions of organolithium aggregates is d...
In Chapter I of this dissertation, the Skattebol-type rearrangement (in THF solution at -78(DEGREES)...
The effects of lithium alkoxides on the rates of reactions and on the structures of a series of tert...
265 p.Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1997.A series of tin-lithium excha...
Attempts to generate the free bis(N-heterocyclic carbene) vegi<sup>R</sup> (R = <i>n</i>Pr, <i>t</i...
This chapter addresses the reactivity of a-lithiated organohalogens, ethers, and amines. Special emp...
Computational quantum chemistry was used to investigate the structures of lithium carbamates in the ...
Electronic stabilization of the negative charge by a thiophosphinoyl and pyridyl/quinolyl substituen...
The role of O-Lithiated species has a very strong precedence in literature ranging from well-known r...
Computational results are presented to support experimental evidence that cyclopropanation reactions...
Progress toward understanding the reactivity of synthetically important lithium enolates relies on t...
Abstract- The dimerization energies of lithium compounds, 2LiX-(LiX)9, are quite large and depend pr...
The method of continuous variation (MCV) was used in conjunction with <sup>6</sup>Li NMR spectroscop...
Waerder B, Steinhauer S, Neumann B, et al. Solid-State Structure of a Li/F Carbenoid: Pentafluoroeth...
s-Block metal carbenoids are carbene synthons and applied in a myriad of organic transformations. Th...
A multifaceted approach to the study of the structure and reactions of organolithium aggregates is d...
In Chapter I of this dissertation, the Skattebol-type rearrangement (in THF solution at -78(DEGREES)...
The effects of lithium alkoxides on the rates of reactions and on the structures of a series of tert...
265 p.Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1997.A series of tin-lithium excha...
Attempts to generate the free bis(N-heterocyclic carbene) vegi<sup>R</sup> (R = <i>n</i>Pr, <i>t</i...