The indium-promoted allylation of enantiomerically pure N-tert-butylsulfinyl imines has been shown to be a versatile and useful methodology for the preparation of diastereomerically enriched N-protected homoallylamines. The preparation of both enantiomeric diastereomers is possible by changing the stereochemistry of the starting imine. Importantly, the deprotection of the sulfinylamines is easily achieved by acid treatment, and, therefore, the corresponding free amines are accessible in an enantioenriched manner. This methodology has been applied to the synthesis of interesting compounds, that is, mostly alkaloids and a wide representation of naturally occurring products.We are grateful to the Spanish Ministerio de Ciencia e Innovación (CTQ...
Chiral N-(tert-butyl)sulfinyl aldimines easily prepared from commercially available compounds have b...
There has been great interest in developing methods for asymmetric nucleophilic allylic addition of ...
We first report that highly polarized organometallic compounds of s-block elements add smoothly to c...
The indium-promoted allylation of chiral N-sulfinyl imines represents a useful and versatile procedu...
Diastereoselective allylation of imines bearing a chiral auxiliary is a reliable, efficient, and pow...
The reaction of different chiral imines 3 derived from aldehydes or ketones with the silylated propa...
The palladium-catalyzed allylation of N-tert-butanesulfinyl imines with allylic alcohols in the pres...
The catalytic enantioselective addition of allyltributylstannane to N-protected greek small letter a...
The allylation reaction is an ambiphilic reaction depending on the nature of the allylic substituent...
Chiral tert-butylsulfinyl imines 3, which are easily prepared from the corresponding bromo carbonyl ...
[GRAPHICS] The highly diastereoselective addition of allylzinc bromide to imines derived from (R)-ph...
The highly diastereoselective addition of allylzinc bromide to imines derived from (R)-phenylglycine...
The reaction of N-tert-butanesulfinyl imines 1 with 1,3-dibromopropene (2), in the presence of indiu...
Primary allylic amines with enantiomeric excesses from 97 to >99% were prepared by asymmetric transf...
A simple and robust protocol is detailed for the preparation of enantioenriched α-substituted (1,4-p...
Chiral N-(tert-butyl)sulfinyl aldimines easily prepared from commercially available compounds have b...
There has been great interest in developing methods for asymmetric nucleophilic allylic addition of ...
We first report that highly polarized organometallic compounds of s-block elements add smoothly to c...
The indium-promoted allylation of chiral N-sulfinyl imines represents a useful and versatile procedu...
Diastereoselective allylation of imines bearing a chiral auxiliary is a reliable, efficient, and pow...
The reaction of different chiral imines 3 derived from aldehydes or ketones with the silylated propa...
The palladium-catalyzed allylation of N-tert-butanesulfinyl imines with allylic alcohols in the pres...
The catalytic enantioselective addition of allyltributylstannane to N-protected greek small letter a...
The allylation reaction is an ambiphilic reaction depending on the nature of the allylic substituent...
Chiral tert-butylsulfinyl imines 3, which are easily prepared from the corresponding bromo carbonyl ...
[GRAPHICS] The highly diastereoselective addition of allylzinc bromide to imines derived from (R)-ph...
The highly diastereoselective addition of allylzinc bromide to imines derived from (R)-phenylglycine...
The reaction of N-tert-butanesulfinyl imines 1 with 1,3-dibromopropene (2), in the presence of indiu...
Primary allylic amines with enantiomeric excesses from 97 to >99% were prepared by asymmetric transf...
A simple and robust protocol is detailed for the preparation of enantioenriched α-substituted (1,4-p...
Chiral N-(tert-butyl)sulfinyl aldimines easily prepared from commercially available compounds have b...
There has been great interest in developing methods for asymmetric nucleophilic allylic addition of ...
We first report that highly polarized organometallic compounds of s-block elements add smoothly to c...