- In
organic chemistry,
methylenation is a
chemical reaction that
inserts a
methylene (−CH2−)
group into a
chemical compound: A − B ⟶ A − CH 2 − B {\displaystyle...
- doi:10.2174/1389200003339270 Bonthrone, W. & Cornforth, J. (1969). "The
methylenation of catechols".
Journal of the
Chemical Society (9): 1202–1204. doi:10...
-
reagents in
organic synthesis. Tebbe's reagent,
which is used for the
methylenation of
esters and ketones, is
prepared from TMA and
titanocene dichloride...
- In
organic chemistry, the
Lombardo methylenation is a name
reaction that
allows for the
methylenation of
carbonyl compounds with the use of Lombardo's...
-
chemistry Homologation reaction Kauffmann olefination Titanium–zinc
methylenation Maercker, A. Org. React. 1965, 14, 270–490. W. Carruthers, Some Modern...
- (Trimethylsilyl)methyllithium is
classified both as an
organolithium compound and an
organosilicon compound. It has the
empirical formula LiCH2Si(CH3)3...
- 1016/S0040-4039(00)88578-0. Bonthrone, W. & Cornforth, J. (1969). "The
methylenation of catechols".
Journal of the
Chemical Society (9): 1202–1204. doi:10...
- The
Nysted reagent is a
reagent used in
organic synthesis for the
methylenation of a
carbonyl group. It was
discovered in 1975 by
Leonard N.
Nysted in...
- London, 2000. Pine, S. H.; Kim, V.; Lee, V. (1990). "Enol
ethers by
methylenation of esters: 1-Phenoxy-1-phenylethene and 3,4-dihydro-2-methylene-2H-1-benzopyran"...
-
basis of the
Kulinkovich reaction: "Lombardo's reagent" is used for
methylenation. It is
functionally related to the Dibromomethane-Zinc-Titanium(IV)...
