-
resulting 1,3-dithiane is then
lithiated with the use of butyllithium. The 2-
lithio-1,3-dithiane
reacts with
electrophiles to give a 2-alkyl-1,3-dithiane. Finally...
- thiophene-2-carboxylic acid
undergoes double deprotonation to give the 5-
lithio derivative, a
precursor to many 5-substituted derivatives. Thiophene-2-carboxylic...
- Ene (first
featured on
Phantom on the Horizon). It was
recorded at
Studio Lithio. The
album featured a
slightly less
aggressive style compared to the band's...
-
gives 3-nitrodimethylaniline. It
reacts with
butyllithium to give the 2-
lithio derivative.
Electrophilic methylating agents like
dimethyl sulfate attack...
-
Arylsulfonic acids react with two
equiv of
butyl lithium to give the ortho-
lithio derivatives, i.e., ortho-lithiation.
These dilithio compounds are poised...
- than
imidazoles (pKa = 7).
Deprotonation of
oxazoles occurs at C2, and the
lithio salt
exists in
equilibrium with the ring-opened enolate-isonitrile, which...
- One
method described the
synthesis of
thiothixene by
acetylation of 9-
lithio-N,N-dimethylthioxanthene-2-sulfonamide.
After acetylation, a condensation...
- It
undergoes deprotonation by
methyl lithium to give CH3ONHLi. This N-
lithio derivative is
attacked by
organolithium compounds to give,
after hydrolysis...
-
deprotonated by butyllithium: (CH3)3SiCHN2 + BuLi → (CH3)3SiCLiN2 + BuH The
lithio compound is versatile. From it can be
prepared other trimethylsilyldiazoalkanes:...
- Saint-Gobain
Research North America and
Chief Scientist and co-founder of
Lithios, Inc.
Bazant earned a B.S. in
Mathematics and
Physics in 1992 and an M...
