gliocladin-c and 2-oxindole

gliocladin-c has been researched along with 2-oxindole* in 2 studies

Other Studies

2 other study(ies) available for gliocladin-c and 2-oxindole

Article	Year
Efficient Synthesis of 3,3'-Mixed Bisindoles via Lewis Acid Catalyzed Reaction of Spiro-epoxyoxindoles and Indoles. Organic letters, 2015, Jul-17, Volume: 17, Issue:14 An efficient strategy for the synthesis of 3-(3-indolyl)-oxindole-3-methanol has been developed to achieve a Lewis acid catalyzed, highly regioselective ring opening of spiro-epoxyoxindoles with indoles. The method is used for the gram-scale formal total synthesis of (±)-gliocladin C. Topics: Catalysis; Indoles; Lewis Acids; Molecular Structure; Oxindoles; Piperazines; Pyrrolidinones; Spiro Compounds	2015
Organocatalytic Michael addition of indoles to isatylidene-3-acetaldehydes: application to the formal total synthesis of (-)-chimonanthine. Organic letters, 2013, May-03, Volume: 15, Issue:9 A novel strategy for the enantioselective synthesis of 3,3'-disubstituted oxindoles by the organocatalytic Michael addition of indoles to isatylidene-3-acetaldehydes was developed, which can be used for the formal total synthesis of (-)-chimonanthine and the core structure construction of (+)-gliocladin C. Topics: Acetaldehyde; Catalysis; Indoles; Molecular Structure; Oxindoles; Piperazines; Pyrroles; Pyrrolidinones; Stereoisomerism	2013

Article

Year

Efficient Synthesis of 3,3'-Mixed Bisindoles via Lewis Acid Catalyzed Reaction of Spiro-epoxyoxindoles and Indoles.

Organic letters, 2015, Jul-17, Volume: 17, Issue:14

An efficient strategy for the synthesis of 3-(3-indolyl)-oxindole-3-methanol has been developed to achieve a Lewis acid catalyzed, highly regioselective ring opening of spiro-epoxyoxindoles with indoles. The method is used for the gram-scale formal total synthesis of (±)-gliocladin C.

Topics: Catalysis; Indoles; Lewis Acids; Molecular Structure; Oxindoles; Piperazines; Pyrrolidinones; Spiro Compounds

2015

Organocatalytic Michael addition of indoles to isatylidene-3-acetaldehydes: application to the formal total synthesis of (-)-chimonanthine.

Organic letters, 2013, May-03, Volume: 15, Issue:9

A novel strategy for the enantioselective synthesis of 3,3'-disubstituted oxindoles by the organocatalytic Michael addition of indoles to isatylidene-3-acetaldehydes was developed, which can be used for the formal total synthesis of (-)-chimonanthine and the core structure construction of (+)-gliocladin C.

Topics: Acetaldehyde; Catalysis; Indoles; Molecular Structure; Oxindoles; Piperazines; Pyrroles; Pyrrolidinones; Stereoisomerism

2013