Indoline alkaloids constitute a large class of natural products; their diverse and complex
structures contribute to potent biological activities in a range of molecules. Designing an …

A concise asymmetric total synthesis of (−)-communesin F (∼ 6% overall yield in the longest
linear sequence of 19 steps) is described. It features an unprecedented intramolecular …

The first catalytic asymmetric total synthesis of the heptacyclic alkaloid (−)-communesin F is
described. A key step features an iridium-catalyzed asymmetric intermolecular cascade …

Enantioselective Total Syntheses of Communesins A and B × Close The Infona portal uses
cookies, ie strings of text saved by a browser on the user's device. The portal can access …

The first asymmetric total synthesis of (+)-perophoramidine has been achieved in 17 steps
with∼ 11% overall yield. The key step relies on an asymmetric biomimetic Diels− Alder …

A concise total synthesis of (±)-communesin F has been completed in 15 linear steps from 4-
bromotryptophol in an overall yield of 6.7%. A key step features the cycloaddition of indol-2 …

In 1993, Numata et al. isolated two unique natural products from a Penicillium mold found
growing on the marine alga Enteromorpha intestinalis.[1] The structures of these …

Communesins A–H are a growing family of natural products isolated from a marine fungal
strain of Penicillium species. Preliminary biological evaluation has revealed that these …

Expedient synthetic approaches to the highly functionalized polycyclic alkaloids
communesin F and perophoramidine are described using a unified approach featuring a key …

An efficient, unified, and stereodivergent approach toward communesin F and
perophoramidine was examined. The C (3) all-carbon quaternary center of an oxindole was …