The Journal of Organic Chemistry

Metabolites of the marine sponge Laxosuberites species

DB Stierle, DJ Faulkner

Index: Stierle, Donald B.; Faulkner, John D. Journal of Organic Chemistry, 1980 , vol. 45, # 24 p. 4980 - 4982

Full Text: HTML

Citation Number: 34

Abstract

In 1975, Cimino et al.'reported the isolation of a series of 3-alkylpyrrole-~!-carboxaldehydes from the marine sponge Oscarella lobularis. During our studies on Indo-Pacific sponges, we obtained a group of alkylated pyrrole-2-carboxaldehydes from Laxosuberites sp. We have shown that these metabolites are pyrrole-2-carboxaldehydes substitui ed at the 5-position by various alkyl groups.

Related Articles:

Synthesis of pyrrolizin-3-ones by flash vacuum pyrolysis of pyrrol-2-ylmethylidene Meldrum's acid derivatives and 3-(pyrrol-2-yl) propenoic esters

[Campbell, Shirley E.; Comer, Murray C.; Derbyshire, Paul A.; Despinoy, Xavier L. M.; McNab, Hamish; Morrison, Roderick; Sommerville, Craig C.; Thornley, Craig Journal of the Chemical Society - Perkin Transactions 1, 1997 , # 15 p. 2195 - 2202]

Novel substituent orientation in Reimer-Tiemann reactions of pyrrole-2-carboxylates

[Smith, Kevin M.; Bobe, Frank W.; Minnetian, Ohannes M.; Hope, Hakon; Yanuck, Michael D. Journal of Organic Chemistry, 1985 , vol. 50, # 6 p. 790 - 792]

More Articles...