The first phosphinine 2-carboxaldehyde was synthesized as shown and transformed into an alkene via a Wittig reaction without destruction of the phosphinine ring
In the first chapter, a phosphine-mediated multi-component reaction between o-phthalaldehydes, nucle...
Three stable alkylidenephosphiranes have been synthesized from the addition of the terminal phosphin...
Two types of phosphinic acids were prepared: N,N-bis(carboxymethyl)aminomethyl phosphinic acid and c...
The first phosphinine 2-carboxaldehyde was synthesized as shown and transformed into an alkene via a...
The first phosphinine 2-carboxaldehyde was synthesized as shown and transformed into an alkene via a...
The Wittig reaction is the chemical reaction of an aldehyde or ketone with a triphenyl phosphonium y...
The Wittig reaction is one of the most common and valuable methods for the formation of alkenes, st...
The formation of C=C bonds is of great importance for fundamental and industrial synthetic organic c...
Under gas-liquid phase-transfer catalysis conditions, an aldehyde passed in the gaseous state throug...
A room-temperature-stable crystalline 2<i>H</i>-phosphirene (<b>1</b>) was prepared by treatment of ...
The Wittig reaction enables the synthesis of an alkene from the reaction of an aldehyde or ketone wi...
<div><p></p><p>The reaction of (hydroxymethyl)triphenylphosphonium with benzylic or allylic halide u...
The transient phosphinidene complex [PhP-Mo(CO) 5], as generated from the appropriate 7-phosphanorbo...
We report a transformation between a well‐known nucleophile, phosphonium ylide, and an electrophile....
Carbonyl olefinations are among the most important organic syntheses that form C=C bonds, as they us...
In the first chapter, a phosphine-mediated multi-component reaction between o-phthalaldehydes, nucle...
Three stable alkylidenephosphiranes have been synthesized from the addition of the terminal phosphin...
Two types of phosphinic acids were prepared: N,N-bis(carboxymethyl)aminomethyl phosphinic acid and c...
The first phosphinine 2-carboxaldehyde was synthesized as shown and transformed into an alkene via a...
The first phosphinine 2-carboxaldehyde was synthesized as shown and transformed into an alkene via a...
The Wittig reaction is the chemical reaction of an aldehyde or ketone with a triphenyl phosphonium y...
The Wittig reaction is one of the most common and valuable methods for the formation of alkenes, st...
The formation of C=C bonds is of great importance for fundamental and industrial synthetic organic c...
Under gas-liquid phase-transfer catalysis conditions, an aldehyde passed in the gaseous state throug...
A room-temperature-stable crystalline 2<i>H</i>-phosphirene (<b>1</b>) was prepared by treatment of ...
The Wittig reaction enables the synthesis of an alkene from the reaction of an aldehyde or ketone wi...
<div><p></p><p>The reaction of (hydroxymethyl)triphenylphosphonium with benzylic or allylic halide u...
The transient phosphinidene complex [PhP-Mo(CO) 5], as generated from the appropriate 7-phosphanorbo...
We report a transformation between a well‐known nucleophile, phosphonium ylide, and an electrophile....
Carbonyl olefinations are among the most important organic syntheses that form C=C bonds, as they us...
In the first chapter, a phosphine-mediated multi-component reaction between o-phthalaldehydes, nucle...
Three stable alkylidenephosphiranes have been synthesized from the addition of the terminal phosphin...
Two types of phosphinic acids were prepared: N,N-bis(carboxymethyl)aminomethyl phosphinic acid and c...
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