Concepedia

Convergent syntheses of the pyrrolic marine natural products lamellarin-O, lamellarin-Q, lukianol-A and some more highly oxygenated congeners

Martin G. Banwell, Bernard L. Flynn, Ernest Hamel, David C. R. Hockless

Chemical Communications · 1997 · 69 citations · 18 references

DOI

Concepts

Abstract

The marine alkaloids lamellarin-Q 1, lamellarin-O 2 and lukianol-A 3 as well as their more highly oxygenated congeners 22 and 23 are synthesised using Stille, Suzuki or Negishi cross-coupling reactions as the key step.

References

18

The Palladium‐Catalyzed Cross‐Coupling Reactions of Organotin Reagents with Organic Electrophiles [New Synthetic Methods (58)]

J. K. Stille · Angewandte Chemie International Edition in English · 1986 · 3.4K citations

, , +9

Metabolites of the marine prosobranch mollusk Lamellaria sp

Raymond J. Andersen, D. John Faulkner, Cun Heng He et al. · Journal of the American Chemical Society · 1985 · 323 citations

, , +8

New synthetic transformations via organoboron compounds

Akira Suzuki · Pure and Applied Chemistry · 1994 · 299 citations · Full text

, , +8

N-(Triisopropylsilyl)pyrrole. A progenitor "par excellence" of 3-substituted pyrroles

Brian L. Bray, Peter Mathies, Reto Naef et al. · The Journal of Organic Chemistry · 1990 · 233 citations

, , +7

New alkaloids of the lamellarin class from the marine ascidian Didemnum chartaceum (Sluiter, 1909)

Niels Lindquist, William Fenical, Gregory D. Van Duyne et al. · The Journal of Organic Chemistry · 1988 · 142 citations

, , +12