Lamellarins are natural products with a [3, 4]-fused pyrrolocoumarin skeleton possessing
interesting biological properties. More than 70 members have been isolated from diverse …

Isoquinoline-enrooted organic small-molecules represent a challenging molecular target in
the organic synthesis arsenal attributed of its structural diversity and therapeutic importance …

We have developed a copper-catalyzed synthesis of pyrrolo [2, 1-a] isoquinolines with
terminal alkynes, aldehydes, and tetrahydroisoquinolines. A variety of pyrrolo [2, 1-a] …

Both chromenone and pyrrolo [2, 1-a] isoquinolines (containing ring-junction nitrogen) are
privileged scaffolds in the field of synthetic as well as medicinal chemistry. These fused …

A Two-Step Approach to a Hexacyclic Lamellarin Core via 1,3-Dipolar Cycloaddition of
Isoquinolinium Ylides to Nitrostilbenes | The Journal of Organic Chemistry Recently Viewed …

We have developed an iron-catalyzed synthesis of pyrrolo [2, 1-a] isoquinoline derivatives
with tetrahydroisoquinolines, arylacyl bromides, and nitroolefins. Highly functionalized …

An efficient domino approach has been developed for the synthesis of polyheterocyclic
derivatives constituting pyrrole moiety. Lewis acid catalyzed reaction of 2‐substituted‐2 …

Lamellarin D trimethyl ether was prepared by 1, 3-dipolar cycloaddition of 6, 7-
dimethoxyisoquinolinium ylide to pentamethoxy-substituted nitrostilbene followed by a …

The three-component domino reaction involving 1-aroyl-3, 4-dihydroisoquinolines, terminal
alkynes, and cyclic NH-acids is a new method for the synthesis of 5, 6-dihydropyrrolo [2, 1-a] …

An elegant and highly concise strategy for the construction of coumarin-functionalized
pyrrolo [2, 1-a] isoquinolines from available propargylamines and isoquinolinium N-ylides …