Add to ORKGAn intramolecular Diels-Alder (IMDA) approach towards the synthesis of a newly isolated biaryl compound, Afzellindanone, is discussed.Bachelor of Science in Chemistry and Biological Chemistr
This thesis describes synthetic studies directed towards the total synthesis of the nakafuran and fl...
Heterocyclic imines provide biaryl products by a two-step transformation. The first transformation i...
The Diels–Alder reaction that involves a nitrogen atom in the diene or dienophile is termed the aza-...
An intramolecular Diels-Alder (IMDA) approach towards the synthesis of a newly isolated biaryl comp...
Intramolecular Diels-Alder (IMDA) reactions are an important class of reactions in synthetic organic...
Graduation date: 2008An expedient approach to the synthesis of a wide range of highly programmable b...
[Introduction] The Diels-Aider reaction is one of the most powerful and widely exploited methods av...
We report the combination of an intramolecular Diels-Alder (IMDA) reaction and a desymmetrisation pr...
The work described in this thesis focused on developing a method to synthesise a variety of organic ...
Diels-Alder (D-A) reaction is undoubtedly the most powerful [4 + 2] cycloaddition reaction in organi...
The Diels-Alder reaction has become a prominent synthetic tool due to the effectiveness for which it...
Efforts directed toward the synthesis of a basiliolide/transtaganolide model system are disclosed. A...
Since the reactivity and selectivity of IMDA(intramolecular Diels-Alder) reactions are often highly ...
The aim of the project was to synthesise (−)-morphine utilising a tethered intramolecular imino-Diel...
A series of trienes possessing internally-activated vinylic sulfone dienophilic groups undergo intra...
This thesis describes synthetic studies directed towards the total synthesis of the nakafuran and fl...
Heterocyclic imines provide biaryl products by a two-step transformation. The first transformation i...
The Diels–Alder reaction that involves a nitrogen atom in the diene or dienophile is termed the aza-...
An intramolecular Diels-Alder (IMDA) approach towards the synthesis of a newly isolated biaryl comp...
Intramolecular Diels-Alder (IMDA) reactions are an important class of reactions in synthetic organic...
Graduation date: 2008An expedient approach to the synthesis of a wide range of highly programmable b...
[Introduction] The Diels-Aider reaction is one of the most powerful and widely exploited methods av...
We report the combination of an intramolecular Diels-Alder (IMDA) reaction and a desymmetrisation pr...
The work described in this thesis focused on developing a method to synthesise a variety of organic ...
Diels-Alder (D-A) reaction is undoubtedly the most powerful [4 + 2] cycloaddition reaction in organi...
The Diels-Alder reaction has become a prominent synthetic tool due to the effectiveness for which it...
Efforts directed toward the synthesis of a basiliolide/transtaganolide model system are disclosed. A...
Since the reactivity and selectivity of IMDA(intramolecular Diels-Alder) reactions are often highly ...
The aim of the project was to synthesise (−)-morphine utilising a tethered intramolecular imino-Diel...
A series of trienes possessing internally-activated vinylic sulfone dienophilic groups undergo intra...
This thesis describes synthetic studies directed towards the total synthesis of the nakafuran and fl...
Heterocyclic imines provide biaryl products by a two-step transformation. The first transformation i...
The Diels–Alder reaction that involves a nitrogen atom in the diene or dienophile is termed the aza-...