The elaboration of the first organophosphorus-catalyzed diaza-Wittig reaction is reported. This catalytic reaction is applied to the synthesis of substituted pyridazine and phthalazine derivatives bearing electron-withdrawing groups with good to excellent yields from substrates containing a diazo functionality as the starting material and a phospholene oxide as the catalyst.status: publishe
An efficient protocol for the synthesis of highly functionalized furans via intramolecular Wittig re...
Diazo compounds are useful synthetic intermediates in organic synthesis but, due to their toxicity a...
A simple versatile method for the conversion of 1-aroyl-2-( substituted benzylidene)-hydrazines to 1...
The elaboration of the first organophosphorus-catalyzed diaza-Wittig reaction is reported. This cata...
A convenient and selective synthesis of 6-substituted-4-hydroxy-3- methoxycarbonyl pyridazines has b...
The first synthesis of novel fused pyridazines has been realized starting from 1,3-diketones involvi...
A new one-pot strategy for the synthesis of phthalazines and pyridazino-aromatics starting from arom...
This review surveys the literature regarding the development of catalytic versions of the Wittig and...
A new flexible strategy for the synthesis of diversely functionalized pyridazines from 4-chloro-1,2-...
A new flexible strategy for the synthesis of diversely functionalized pyridazines from 4-chloro-1,2-...
A new flexible strategy for the synthesis of diversely functionalized pyridazines from 4-chloro-1,2-...
A new flexible strategy for the synthesis of diversely functionalized pyridazines from 4-chloro-1,2-...
The reactions of 4,4-dichloro-1,2-diazabuta-1,3-dienes with dimethyl malonate, cyanoacetic esters an...
This thesis describes the development of a new reaction to form indolizines from pyridines, diazo co...
This thesis details recent advances in the field of redox neutral organocatalytic aza-Wittig chemist...
An efficient protocol for the synthesis of highly functionalized furans via intramolecular Wittig re...
Diazo compounds are useful synthetic intermediates in organic synthesis but, due to their toxicity a...
A simple versatile method for the conversion of 1-aroyl-2-( substituted benzylidene)-hydrazines to 1...
The elaboration of the first organophosphorus-catalyzed diaza-Wittig reaction is reported. This cata...
A convenient and selective synthesis of 6-substituted-4-hydroxy-3- methoxycarbonyl pyridazines has b...
The first synthesis of novel fused pyridazines has been realized starting from 1,3-diketones involvi...
A new one-pot strategy for the synthesis of phthalazines and pyridazino-aromatics starting from arom...
This review surveys the literature regarding the development of catalytic versions of the Wittig and...
A new flexible strategy for the synthesis of diversely functionalized pyridazines from 4-chloro-1,2-...
A new flexible strategy for the synthesis of diversely functionalized pyridazines from 4-chloro-1,2-...
A new flexible strategy for the synthesis of diversely functionalized pyridazines from 4-chloro-1,2-...
A new flexible strategy for the synthesis of diversely functionalized pyridazines from 4-chloro-1,2-...
The reactions of 4,4-dichloro-1,2-diazabuta-1,3-dienes with dimethyl malonate, cyanoacetic esters an...
This thesis describes the development of a new reaction to form indolizines from pyridines, diazo co...
This thesis details recent advances in the field of redox neutral organocatalytic aza-Wittig chemist...
An efficient protocol for the synthesis of highly functionalized furans via intramolecular Wittig re...
Diazo compounds are useful synthetic intermediates in organic synthesis but, due to their toxicity a...
A simple versatile method for the conversion of 1-aroyl-2-( substituted benzylidene)-hydrazines to 1...