A new series of organocatalysts able to catalyse Diels-Alder cycloaddition reactions of \u3b1,\u3b2-unsaturated aldehydes was studied from both synthetic and theoretical perspectives. The importance of the imidazolidinone scaffold and the influence of the functional groups upon the formation of the reactive species was evaluated. Moreover taking into account that all these new organocatalysts gave the exo-cycloadducts as the major isomers with high selectivity a theoretical study was realized to try and define the essential features determining the observed stereochemical preference
Homochiral N-enoylimidazolidin-2-ones 5-8 are readily accessible, practical, and highly diastereosel...
Abstract: Diels-Alder reactions have emerged as highly powerful transformations for the generation o...
α,β-Unsaturated acylammonium salts, generated in situ from commodity acid chlorides and a chiral iso...
The development of new catalytic reactions, particularly synthetically efficient cascade processes f...
While organocatalysis has emerged as a significant component in modern organic synthesis, being reco...
The development of novel, high-yielding, and selective methodologies for the asymmetric synthesis of...
The development of novel, high-yielding, and selective methodologies for the asymmetric synthesis of...
The mechanism and enantioselectivity of the organocatalytic Diels-Alder reaction were computationall...
The development of new catalytic reactions, particularly synthetically efficient cascade processes f...
It has been known that substituents have a significant effect on the reactivity and selectivity of t...
Functionalization of carbonyl compounds has been intensively studied for a long time as carbonyl com...
Functionalization of carbonyl compounds has been intensively studied for a long time as carbonyl com...
A range of pyrazolidin-3-ones have been prepared and their activity as catalysts for iminium-ion pro...
[Introduction] The Diels-Aider reaction is one of the most powerful and widely exploited methods av...
A range of pyrazolidin-3-ones have been prepared and their activity as catalysts for iminium-ion pro...
Homochiral N-enoylimidazolidin-2-ones 5-8 are readily accessible, practical, and highly diastereosel...
Abstract: Diels-Alder reactions have emerged as highly powerful transformations for the generation o...
α,β-Unsaturated acylammonium salts, generated in situ from commodity acid chlorides and a chiral iso...
The development of new catalytic reactions, particularly synthetically efficient cascade processes f...
While organocatalysis has emerged as a significant component in modern organic synthesis, being reco...
The development of novel, high-yielding, and selective methodologies for the asymmetric synthesis of...
The development of novel, high-yielding, and selective methodologies for the asymmetric synthesis of...
The mechanism and enantioselectivity of the organocatalytic Diels-Alder reaction were computationall...
The development of new catalytic reactions, particularly synthetically efficient cascade processes f...
It has been known that substituents have a significant effect on the reactivity and selectivity of t...
Functionalization of carbonyl compounds has been intensively studied for a long time as carbonyl com...
Functionalization of carbonyl compounds has been intensively studied for a long time as carbonyl com...
A range of pyrazolidin-3-ones have been prepared and their activity as catalysts for iminium-ion pro...
[Introduction] The Diels-Aider reaction is one of the most powerful and widely exploited methods av...
A range of pyrazolidin-3-ones have been prepared and their activity as catalysts for iminium-ion pro...
Homochiral N-enoylimidazolidin-2-ones 5-8 are readily accessible, practical, and highly diastereosel...
Abstract: Diels-Alder reactions have emerged as highly powerful transformations for the generation o...
α,β-Unsaturated acylammonium salts, generated in situ from commodity acid chlorides and a chiral iso...