International audienceThe formal synthesis of (±)-mersicarpine was achieved using an lntermolecular radical addition-radical cyclization cascade. This key reaction represents a flexible, convergent route to numerous polycyclic indole derivatives. © 2009 American Chemical Society
AbstractA Unified Approach Toward the Total Syntheses ofPrenylated Indole Alkaloid Natural Productsb...
The most preferred heterocyclic indole core was de novo assembled by an innovative 2-step reaction f...
The use of small molecule chemical probes is highly attractive in dissecting complex biological proc...
International audienceThe formal synthesis of (±)-mersicarpine was achieved using an lntermolecular ...
Inspired by their potential biosynthesis, we have developed divergent total syntheses of seven monot...
An acid-promoted novel cascade cyclization is described. Using 8 equiv of trifluoroacetic acid or a ...
Polycyclic indolines are the common and core structural motif of many indole alkaloids that usually ...
We present the unprecedented reaction of a [3+3] cyclization of indol-2-yl carbinol with azadiene fo...
This dissertation presents three main projects. The first discusses synthetic strategies towards the...
Subsequent reduction and dearomatizing cyclization reactions open up an entry into the synthesis of ...
A modular and streamlined synthetic strategy for the generation of bridged indole alkaloid-like hete...
Development of novel synthetic methodologies and their application to synthesis of natural products ...
A modular and streamlined synthetic strategy for the generation of bridged indole alkaloid-like hete...
A reliable synthetic route to fused polycyclic indolines is documented by the development of a stere...
Indoline-fused polycycles have been synthesized through a TFA-promoted intramolecular dearomative cy...
AbstractA Unified Approach Toward the Total Syntheses ofPrenylated Indole Alkaloid Natural Productsb...
The most preferred heterocyclic indole core was de novo assembled by an innovative 2-step reaction f...
The use of small molecule chemical probes is highly attractive in dissecting complex biological proc...
International audienceThe formal synthesis of (±)-mersicarpine was achieved using an lntermolecular ...
Inspired by their potential biosynthesis, we have developed divergent total syntheses of seven monot...
An acid-promoted novel cascade cyclization is described. Using 8 equiv of trifluoroacetic acid or a ...
Polycyclic indolines are the common and core structural motif of many indole alkaloids that usually ...
We present the unprecedented reaction of a [3+3] cyclization of indol-2-yl carbinol with azadiene fo...
This dissertation presents three main projects. The first discusses synthetic strategies towards the...
Subsequent reduction and dearomatizing cyclization reactions open up an entry into the synthesis of ...
A modular and streamlined synthetic strategy for the generation of bridged indole alkaloid-like hete...
Development of novel synthetic methodologies and their application to synthesis of natural products ...
A modular and streamlined synthetic strategy for the generation of bridged indole alkaloid-like hete...
A reliable synthetic route to fused polycyclic indolines is documented by the development of a stere...
Indoline-fused polycycles have been synthesized through a TFA-promoted intramolecular dearomative cy...
AbstractA Unified Approach Toward the Total Syntheses ofPrenylated Indole Alkaloid Natural Productsb...
The most preferred heterocyclic indole core was de novo assembled by an innovative 2-step reaction f...
The use of small molecule chemical probes is highly attractive in dissecting complex biological proc...
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