The development of micellar catalysis offers a sustainable alternative to organic solvents representing an environmental milestone in organic synthesis. Here the first Michael addition of masked acetaldehyde under neutral, cationic and anionic micellar catalysis is reported, affording the products in high yields and enantiomeric excess in spite the use of water as solvent
A simple and more efficient method has been developed for the synthesis of 2-amino-4H-benzo[b]pyrans...
The present review paper deals with the development of catalytic systems in water in the presence of...
Reducing the use of solvents is an important aim of green chemistry. Using micelles self-assembled f...
Green Chemistry has become a priority for conducting chemistry in both academia and industry. When a...
4Replacement of organic solvents, in particular chlorinated, aromatic, and polar aprotic ones, is an...
The micellar approach, whose major feature is the possibility to operate in water as the reaction me...
Designer surfactants as specific amphiphilic neutral compounds for micellar catalysis has revolution...
Micelles can affect the rate, stereo-, regio- and enantioselectivity of organic reactions. ¹²³ This ...
As clearly described in the series of illustrative examples\ud reported above, the use of micellar e...
Highly enantioselective biomimetic Michael addition reactions of malonic acid half thioesters (MAHTs...
Water is considered a green, sustainable, and inexpensive solvent for organic synthesis. However, pe...
Organocatalytic, asymmetric Mannich reactions giving beta3-amino acid derivatives have been reviewed...
The purpose of the work described in this thesis was the synthesis of a new class of surfactants con...
Stereocontrolled formation of carbon-carbon and carbon-heteroatom bonds through asymmetric organocat...
The use of water as a solvent for chemical transformations and catalysis is not only a counter-intui...
A simple and more efficient method has been developed for the synthesis of 2-amino-4H-benzo[b]pyrans...
The present review paper deals with the development of catalytic systems in water in the presence of...
Reducing the use of solvents is an important aim of green chemistry. Using micelles self-assembled f...
Green Chemistry has become a priority for conducting chemistry in both academia and industry. When a...
4Replacement of organic solvents, in particular chlorinated, aromatic, and polar aprotic ones, is an...
The micellar approach, whose major feature is the possibility to operate in water as the reaction me...
Designer surfactants as specific amphiphilic neutral compounds for micellar catalysis has revolution...
Micelles can affect the rate, stereo-, regio- and enantioselectivity of organic reactions. ¹²³ This ...
As clearly described in the series of illustrative examples\ud reported above, the use of micellar e...
Highly enantioselective biomimetic Michael addition reactions of malonic acid half thioesters (MAHTs...
Water is considered a green, sustainable, and inexpensive solvent for organic synthesis. However, pe...
Organocatalytic, asymmetric Mannich reactions giving beta3-amino acid derivatives have been reviewed...
The purpose of the work described in this thesis was the synthesis of a new class of surfactants con...
Stereocontrolled formation of carbon-carbon and carbon-heteroatom bonds through asymmetric organocat...
The use of water as a solvent for chemical transformations and catalysis is not only a counter-intui...
A simple and more efficient method has been developed for the synthesis of 2-amino-4H-benzo[b]pyrans...
The present review paper deals with the development of catalytic systems in water in the presence of...
Reducing the use of solvents is an important aim of green chemistry. Using micelles self-assembled f...