A 2328-membered library of 2,3,4-trisubstituted tetrahydroquinolines was produced using a combination of solution- and solid-phase synthesis techniques. A tetrahydroquinoline (THQ) scaffold was prepared via an asymmetric Povarov reaction using cooperative catalysis to generate three contiguous stereogenic centers. A matrix of 4 stereoisomers of the THQ scaffold was prepared to enable the development of stereo/structure-activity relationships (SSAR) upon biological testing. A sparse matrix design strategy was employed to select library members to be synthesized with the goal of generating a diverse collection of tetrahydroquinolines with physicochemical properties suitable for downstream discovery.Chemistry and Chemical Biolog
The tetrahydroquinolines obtained through the Povarov multicomponent reaction have been oxidized to ...
A new method is reported for effecting catalytic enantioselective intramolecular [5+2] cycloaddition...
Rh-catalysed conjugate additions of 2-aminophenyl boronic acid derivatives were exploited in diaster...
A 2328-membered library of 2,3,4-trisubstituted tetrahydroquinolines was produced using a combinatio...
A 2328-membered library of 2,3,4-trisubstituted tetrahydroquinolines was produced using a combinatio...
[Excerpt] 1,2,3,4-Tetrahydroquinolines (THQ) had shown diverse biological activities such as antiarr...
An easy and efficient synthetic methodology for the one-pot stereocontrolled synthesis of tetrahydro...
An easy and efficient synthetic methodology for the one-pot stereocontrolled synthesis of tetrahydro...
With the goal of developing a library synthesis of tetrahydroquinoline-derived natural-product-like ...
The research presented herein explores three aspects of asymmetric catalysis: (1) the development of...
The tetrahydroquinolines structural unit is found in a number of natural products that exhibit a var...
The synthesis of novel tetrahydroquinolines (THQ) and dihydroquinolines (DHQ) are reported using thr...
none3noThe Povarov reaction provides a straightforward and modular entry to 1,2,3,4-tetrahydroquinol...
The Povarov reaction provides a straightforward and modular entry to 1,2,3,4-tetrahydroquinolines (T...
The Povarov reaction provides a straightforward and modular entry to 1,2,3,4-tetrahydroquinolines (T...
The tetrahydroquinolines obtained through the Povarov multicomponent reaction have been oxidized to ...
A new method is reported for effecting catalytic enantioselective intramolecular [5+2] cycloaddition...
Rh-catalysed conjugate additions of 2-aminophenyl boronic acid derivatives were exploited in diaster...
A 2328-membered library of 2,3,4-trisubstituted tetrahydroquinolines was produced using a combinatio...
A 2328-membered library of 2,3,4-trisubstituted tetrahydroquinolines was produced using a combinatio...
[Excerpt] 1,2,3,4-Tetrahydroquinolines (THQ) had shown diverse biological activities such as antiarr...
An easy and efficient synthetic methodology for the one-pot stereocontrolled synthesis of tetrahydro...
An easy and efficient synthetic methodology for the one-pot stereocontrolled synthesis of tetrahydro...
With the goal of developing a library synthesis of tetrahydroquinoline-derived natural-product-like ...
The research presented herein explores three aspects of asymmetric catalysis: (1) the development of...
The tetrahydroquinolines structural unit is found in a number of natural products that exhibit a var...
The synthesis of novel tetrahydroquinolines (THQ) and dihydroquinolines (DHQ) are reported using thr...
none3noThe Povarov reaction provides a straightforward and modular entry to 1,2,3,4-tetrahydroquinol...
The Povarov reaction provides a straightforward and modular entry to 1,2,3,4-tetrahydroquinolines (T...
The Povarov reaction provides a straightforward and modular entry to 1,2,3,4-tetrahydroquinolines (T...
The tetrahydroquinolines obtained through the Povarov multicomponent reaction have been oxidized to ...
A new method is reported for effecting catalytic enantioselective intramolecular [5+2] cycloaddition...
Rh-catalysed conjugate additions of 2-aminophenyl boronic acid derivatives were exploited in diaster...