In this Account strategies using zeolites as media to achieve chiral induction are presented. Diastereomeric excesses as high as 90% and enantiomeric excesses up to 78% have been obtained with selected systems within zeolites. The same systems show no asymmetric induction in solution. Chiral induction is dependent on the alkali ions present in the zeolites. Alkali ions control not only the extent of asymmetric induction but often the isomer being enhanced. Results of ab initio computations have allowed us to gain an insight into the observed selectivity within zeolites
Alkali ion-exchanged Y-zeolites significantly enhance asymmetric induction in the photoisomerization...
By employing a strategy that involves the use of chirally modified zeolite as the reaction medium, m...
Employing the photobehavior of tropolone alkyl ethers as the probe, we have established that cyclode...
The confined spaces of zeolites have been found to be ideal for carrying out enantio- and diastereo-...
From the perspective of asymmetric induction, the photochemistry of 24 chiral esters and amides of c...
Irradiation of 2-benzoyladamantane derivatives in zeolites yields the endo-cyclobutanols as the only...
From the perspective of asymmetric induction, the photochemistry of 24 chiral esters and amides of c...
Three different approaches to asymmetric induction in the cis-to-trans photoisomerization of a numbe...
Two strategies, namely chiral inductor and chiral auxiliary approaches, have been examined within ze...
The photochemistry of 31 α-oxoamides capable of undergoing ?γ-hydrogen transfer has been examined wi...
Asymmetric induction in photochemical reactions has been explored using the photochemistry of tropol...
With Nature as role model, chemists have utilized confined media to achieve selectivity in chemical ...
Zeolites significantly enhance the influence of chiral auxiliaries during photochemical reactions. T...
Moderate enantioslectivity has been achieved on two photochemical reactions that involve molecules r...
Photochemistry of optically pure trans-2,3-diphenyl-1-benzoylcyclopropane has been examined in isotr...
Alkali ion-exchanged Y-zeolites significantly enhance asymmetric induction in the photoisomerization...
By employing a strategy that involves the use of chirally modified zeolite as the reaction medium, m...
Employing the photobehavior of tropolone alkyl ethers as the probe, we have established that cyclode...
The confined spaces of zeolites have been found to be ideal for carrying out enantio- and diastereo-...
From the perspective of asymmetric induction, the photochemistry of 24 chiral esters and amides of c...
Irradiation of 2-benzoyladamantane derivatives in zeolites yields the endo-cyclobutanols as the only...
From the perspective of asymmetric induction, the photochemistry of 24 chiral esters and amides of c...
Three different approaches to asymmetric induction in the cis-to-trans photoisomerization of a numbe...
Two strategies, namely chiral inductor and chiral auxiliary approaches, have been examined within ze...
The photochemistry of 31 α-oxoamides capable of undergoing ?γ-hydrogen transfer has been examined wi...
Asymmetric induction in photochemical reactions has been explored using the photochemistry of tropol...
With Nature as role model, chemists have utilized confined media to achieve selectivity in chemical ...
Zeolites significantly enhance the influence of chiral auxiliaries during photochemical reactions. T...
Moderate enantioslectivity has been achieved on two photochemical reactions that involve molecules r...
Photochemistry of optically pure trans-2,3-diphenyl-1-benzoylcyclopropane has been examined in isotr...
Alkali ion-exchanged Y-zeolites significantly enhance asymmetric induction in the photoisomerization...
By employing a strategy that involves the use of chirally modified zeolite as the reaction medium, m...
Employing the photobehavior of tropolone alkyl ethers as the probe, we have established that cyclode...