Smooth and efficient reaction conditions have been found for the transformation of protected β-hydroxyacylsilanes into the corresponding aldehydes. This opens a new route to iterative aldol reactions, and it has been used for the synthesis of fragments of several bioactive natural products
This paper describes the substrate specificity, synthetic scope, and efficiency of aldolase catalyti...
Boron and tin(II) 2-furanolates generated in situ from 2-(5H)-furanone and α-angelica lactone underg...
Copyright © 2013 Heli Kylmälä, et al. This is an open access article distributed under the Creative ...
International audienceSmooth and efficient reaction conditions have been found for the transformatio...
La réaction d'aldolisation est une des méthodes les plus importantes et plus utilisées pour former d...
A novel organocatalyzed direct aldol reaction of aldehydes to silyl glyoxylates is disclosed. This m...
International audienceAldolases are key biocatalysts for stereoselective C–C bond formation allowing...
The combination of triethylamine, magnesium(II) perchlorate and bipyridine generates a catalyst syst...
International audienceA simple and efficient method for the prepn. of β-hydroxyacylsilanes has been ...
The asymmetric aldol reaction with formaldehyde is a fundamental carbon-carbon bond-forming reaction...
An uncatalyzed aldol-type reaction of aromatic N-trimethylsilyl ketene imines with O-protected -tria...
Free aldopentoses and aldohexoses reacted respectively with (EtO)2P(O)CHNaCOAr to give the five ster...
Free aldopentoses and aldohexoses reacted respectively with (EtO)2P(O)CHNaCOAr to give the five ster...
The aldol-type condensation between \u3b1-dibenzylamino trimethylsilyl ketene acetals and various ac...
The intramolecular aldol condensation of 3-oxocyclohexaneacetaldehydes leading to C(6) epimeric mixt...
This paper describes the substrate specificity, synthetic scope, and efficiency of aldolase catalyti...
Boron and tin(II) 2-furanolates generated in situ from 2-(5H)-furanone and α-angelica lactone underg...
Copyright © 2013 Heli Kylmälä, et al. This is an open access article distributed under the Creative ...
International audienceSmooth and efficient reaction conditions have been found for the transformatio...
La réaction d'aldolisation est une des méthodes les plus importantes et plus utilisées pour former d...
A novel organocatalyzed direct aldol reaction of aldehydes to silyl glyoxylates is disclosed. This m...
International audienceAldolases are key biocatalysts for stereoselective C–C bond formation allowing...
The combination of triethylamine, magnesium(II) perchlorate and bipyridine generates a catalyst syst...
International audienceA simple and efficient method for the prepn. of β-hydroxyacylsilanes has been ...
The asymmetric aldol reaction with formaldehyde is a fundamental carbon-carbon bond-forming reaction...
An uncatalyzed aldol-type reaction of aromatic N-trimethylsilyl ketene imines with O-protected -tria...
Free aldopentoses and aldohexoses reacted respectively with (EtO)2P(O)CHNaCOAr to give the five ster...
Free aldopentoses and aldohexoses reacted respectively with (EtO)2P(O)CHNaCOAr to give the five ster...
The aldol-type condensation between \u3b1-dibenzylamino trimethylsilyl ketene acetals and various ac...
The intramolecular aldol condensation of 3-oxocyclohexaneacetaldehydes leading to C(6) epimeric mixt...
This paper describes the substrate specificity, synthetic scope, and efficiency of aldolase catalyti...
Boron and tin(II) 2-furanolates generated in situ from 2-(5H)-furanone and α-angelica lactone underg...
Copyright © 2013 Heli Kylmälä, et al. This is an open access article distributed under the Creative ...