The partial reduction of a series of heterocycles in THF is described. By adding amine 3 as a proton source and naphthalene as an electron carrier, we were able to produce reductively alkylated pyrrolines and dihydrofurans in moderate to good yields. This reaction does not require liquid ammonia as a solvent, which may have interesting ramifications for large-scale synthesis. Moreover, we were also able to quench the reduction reactions with an acid chloride so performing a reductive acylation reaction. (C) 2000 Elsevier Science Ltd
The reductive alkylation of 3,4-disubstituted pyridines is reported using either sodium in ammonia o...
The preparation and Birch reduction of a series of electron-deficient pyrroles is described. This me...
Six-membered heterocycles containing nitrogen and oxygen are prevalent in natural products and pharm...
The partial reduction of a series of heterocycles in THF is described. By adding amine 3 as a proton...
The partial reduction of electron-deficient pyrroles using either Birch (Li/NH(3)) or ammonia-free (...
The partial reduction of electron-deficient pyridines is described herein. Mono- and disubstituted p...
The reductive aldol reaction of electron deficient aromatic compounds has been investigated and foun...
The reductive aldol reaction of electron deficient aromatic compounds has been investigated and foun...
The Birch reduction of both pyrroles and furans can be quenched with an aldehyde electrophile, thus ...
The partial reduction of N-Boc pyrroles has been explored giving stereoselective routes to disubstit...
The partial reduction of N-Boc pyrroles has been explored giving stereoselective routes to disubstit...
The partial-reduction of aromatic compounds provides an important link between aromatic compounds an...
The partial-reduction of aromatic compounds provides an important link between aromatic compounds an...
The partial-reduction of aromatic compounds provides an important link between aromatic compounds an...
The preparation and Birch reduction of a series of electron-deficient pyrroles is described. This me...
The reductive alkylation of 3,4-disubstituted pyridines is reported using either sodium in ammonia o...
The preparation and Birch reduction of a series of electron-deficient pyrroles is described. This me...
Six-membered heterocycles containing nitrogen and oxygen are prevalent in natural products and pharm...
The partial reduction of a series of heterocycles in THF is described. By adding amine 3 as a proton...
The partial reduction of electron-deficient pyrroles using either Birch (Li/NH(3)) or ammonia-free (...
The partial reduction of electron-deficient pyridines is described herein. Mono- and disubstituted p...
The reductive aldol reaction of electron deficient aromatic compounds has been investigated and foun...
The reductive aldol reaction of electron deficient aromatic compounds has been investigated and foun...
The Birch reduction of both pyrroles and furans can be quenched with an aldehyde electrophile, thus ...
The partial reduction of N-Boc pyrroles has been explored giving stereoselective routes to disubstit...
The partial reduction of N-Boc pyrroles has been explored giving stereoselective routes to disubstit...
The partial-reduction of aromatic compounds provides an important link between aromatic compounds an...
The partial-reduction of aromatic compounds provides an important link between aromatic compounds an...
The partial-reduction of aromatic compounds provides an important link between aromatic compounds an...
The preparation and Birch reduction of a series of electron-deficient pyrroles is described. This me...
The reductive alkylation of 3,4-disubstituted pyridines is reported using either sodium in ammonia o...
The preparation and Birch reduction of a series of electron-deficient pyrroles is described. This me...
Six-membered heterocycles containing nitrogen and oxygen are prevalent in natural products and pharm...