The Wittig reaction is the chemical reaction of an aldehyde or ketone with a triphenyl phosphonium ylide (the Wittig reagent) to afford an alkene and triphenylphosphine oxide. Noteworthy, this reaction results in the synthesis of alkenes in a selective and predictable fashion. Thus, it became as one of the keystone of synthetic organic chemistry, especially in the total synthesis of natural products, where the selectivity of a reaction is paramount of importance. A literature survey disclosed the existence of vast numbers of related reports and comprehensive reviews on the applications of this important name reaction in the total synthesis of natural products. However, the aim of this chapter is to underscore, the applications of the Wittig...
The mechanism of the Wittig reaction has long been a contentious issue in organic chemistry. Even no...
The Wittig reaction has been investigated with the use of a molecular modeling approach utilizing em...
A review, with 91 refs., of stereoselectivity in reactions of stable and reactive ylids, and the app...
The Wittig reaction enables the synthesis of an alkene from the reaction of an aldehyde or ketone wi...
Carbonyl olefinations are among the most important organic syntheses that form C=C bonds, as they us...
The Wittig reaction is one of the most common and valuable methods for the formation of alkenes, st...
Alkenes with a well defined geometric configuration represent an essential class of key intermediate...
Alkenes with a well defined geometric configuration represent an essential class of key intermediate...
Yüksek Lisans teziWittig reaksiyonu organik sentezlerde stereoseçici karbon-karbon çift bağı oluştur...
Alkenes with a well defined geometric configuration represent an essential class of key intermediate...
Yüksek Lisans TeziWittig reaksiyonu organik sentezlerde stereoseçici karbon-karbon çift bağı oluştur...
Educação Superior::Ciências Exatas e da Terra::QuímicaDescribes The Wittig reaction is a chemical re...
Educação Superior::Ciências Exatas e da Terra::QuímicaDescribes The Wittig reaction is a chemical re...
The first base-free catalytic Wittig reaction utilizing readily available Bu<sub>3</sub>P (5 mol %) ...
In the first chapter, a phosphine-mediated multi-component reaction between o-phthalaldehydes, nucle...
The mechanism of the Wittig reaction has long been a contentious issue in organic chemistry. Even no...
The Wittig reaction has been investigated with the use of a molecular modeling approach utilizing em...
A review, with 91 refs., of stereoselectivity in reactions of stable and reactive ylids, and the app...
The Wittig reaction enables the synthesis of an alkene from the reaction of an aldehyde or ketone wi...
Carbonyl olefinations are among the most important organic syntheses that form C=C bonds, as they us...
The Wittig reaction is one of the most common and valuable methods for the formation of alkenes, st...
Alkenes with a well defined geometric configuration represent an essential class of key intermediate...
Alkenes with a well defined geometric configuration represent an essential class of key intermediate...
Yüksek Lisans teziWittig reaksiyonu organik sentezlerde stereoseçici karbon-karbon çift bağı oluştur...
Alkenes with a well defined geometric configuration represent an essential class of key intermediate...
Yüksek Lisans TeziWittig reaksiyonu organik sentezlerde stereoseçici karbon-karbon çift bağı oluştur...
Educação Superior::Ciências Exatas e da Terra::QuímicaDescribes The Wittig reaction is a chemical re...
Educação Superior::Ciências Exatas e da Terra::QuímicaDescribes The Wittig reaction is a chemical re...
The first base-free catalytic Wittig reaction utilizing readily available Bu<sub>3</sub>P (5 mol %) ...
In the first chapter, a phosphine-mediated multi-component reaction between o-phthalaldehydes, nucle...
The mechanism of the Wittig reaction has long been a contentious issue in organic chemistry. Even no...
The Wittig reaction has been investigated with the use of a molecular modeling approach utilizing em...
A review, with 91 refs., of stereoselectivity in reactions of stable and reactive ylids, and the app...