Subsequent reduction and dearomatizing cyclization reactions open up an entry into the synthesis of novel N-fused polycyclic indolines. The dearomatizing cyclization as key step of the sequence proceeds well with Cu(OTf)2 or TfOH as catalyst. At elevated temperature reduction of nitro-substituted precursors with iron under acidic conditions affords a broad variety of polycyclic indolines directly in a two-step cascade reaction in good to excellent yields. Using the developed protocol, the alkaloids Tryptanthrin and Phaitanthrin C have been prepared.peerReviewe
International audienceThe formal synthesis of (±)-mersicarpine was achieved using an lntermolecular ...
Here we describe a facile, tandem synthetic route for indolo[3,2-c]quinolinones, a class of natural ...
A Lewis acid promoted cascade Friedel-Craft/alkyne indol-2-yl cation cyclization/vinyl cation trappi...
Subsequent reduction and dearomatizing cyclization reactions open up an entry into the synthesis of ...
Polycyclic indolines are the common and core structural motif of many indole alkaloids that usually ...
Herein, a copper(II)-catalyzed dearomative cyclization amination of N-(2-aminobenzoyl) indoles is pr...
An acid-promoted novel cascade cyclization is described. Using 8 equiv of trifluoroacetic acid or a ...
Polycyclic scaffolds found in akuammiline alkaloid natural products can be synthesised from ynone-te...
Indoline-fused polycycles have been synthesized through a TFA-promoted intramolecular dearomative cy...
A reliable synthetic route to fused polycyclic indolines is documented by the development of a stere...
A catalytic approach for the preparation of indolines by dearomatizing cyclization is presented. FeC...
A convenient catalytic protocol for efficiently constructing indoline-fused tetrahydroisoquinolines ...
The synthesis of architecturally complex polycyclic fused indolines is achieved in a chemo-, regio-,...
International audienceThis account summarizes our involvement in the development of dearomatization ...
Pyrroloindoles are a key structural motif found in a wide number of biologically active alkaloids. I...
International audienceThe formal synthesis of (±)-mersicarpine was achieved using an lntermolecular ...
Here we describe a facile, tandem synthetic route for indolo[3,2-c]quinolinones, a class of natural ...
A Lewis acid promoted cascade Friedel-Craft/alkyne indol-2-yl cation cyclization/vinyl cation trappi...
Subsequent reduction and dearomatizing cyclization reactions open up an entry into the synthesis of ...
Polycyclic indolines are the common and core structural motif of many indole alkaloids that usually ...
Herein, a copper(II)-catalyzed dearomative cyclization amination of N-(2-aminobenzoyl) indoles is pr...
An acid-promoted novel cascade cyclization is described. Using 8 equiv of trifluoroacetic acid or a ...
Polycyclic scaffolds found in akuammiline alkaloid natural products can be synthesised from ynone-te...
Indoline-fused polycycles have been synthesized through a TFA-promoted intramolecular dearomative cy...
A reliable synthetic route to fused polycyclic indolines is documented by the development of a stere...
A catalytic approach for the preparation of indolines by dearomatizing cyclization is presented. FeC...
A convenient catalytic protocol for efficiently constructing indoline-fused tetrahydroisoquinolines ...
The synthesis of architecturally complex polycyclic fused indolines is achieved in a chemo-, regio-,...
International audienceThis account summarizes our involvement in the development of dearomatization ...
Pyrroloindoles are a key structural motif found in a wide number of biologically active alkaloids. I...
International audienceThe formal synthesis of (±)-mersicarpine was achieved using an lntermolecular ...
Here we describe a facile, tandem synthetic route for indolo[3,2-c]quinolinones, a class of natural ...
A Lewis acid promoted cascade Friedel-Craft/alkyne indol-2-yl cation cyclization/vinyl cation trappi...