fischerindole and carvone

fischerindole has been researched along with carvone* in 1 studies

Other Studies

1 other study(ies) available for fischerindole and carvone

Article	Year
Direct coupling of indoles with carbonyl compounds: short, enantioselective, gram-scale synthetic entry into the hapalindole and fischerindole alkaloid families. Journal of the American Chemical Society, 2004, Jun-23, Volume: 126, Issue:24 The invention of a method for the direct union of indoles and carbonyl compounds (ketones, amides, esters) is described. Using this new method, a short, enantioselective, gram-scale and protecting group-free synthetic entry to the fischerindole and hapalindole indole alkaloid family has been achieved from carvone and indole. Total syntheses of (+)-hapalindole Q and (-)-12-epi-fischerindole U isothiocyanate are reported. The absolute stereochemistry of the latter natural product has also been determined. Topics: Aldehydes; Alkaloids; Cyclohexane Monoterpenes; Indoles; Molecular Structure; Monoterpenes; Stereoisomerism; Terpenes	2004

Article

Year

Direct coupling of indoles with carbonyl compounds: short, enantioselective, gram-scale synthetic entry into the hapalindole and fischerindole alkaloid families.

Journal of the American Chemical Society, 2004, Jun-23, Volume: 126, Issue:24

The invention of a method for the direct union of indoles and carbonyl compounds (ketones, amides, esters) is described. Using this new method, a short, enantioselective, gram-scale and protecting group-free synthetic entry to the fischerindole and hapalindole indole alkaloid family has been achieved from carvone and indole. Total syntheses of (+)-hapalindole Q and (-)-12-epi-fischerindole U isothiocyanate are reported. The absolute stereochemistry of the latter natural product has also been determined.

Topics: Aldehydes; Alkaloids; Cyclohexane Monoterpenes; Indoles; Molecular Structure; Monoterpenes; Stereoisomerism; Terpenes

2004