esermethole and physovenine

esermethole has been researched along with physovenine* in 2 studies

Other Studies

2 other study(ies) available for esermethole and physovenine

Article	Year
Synthesis of pyrroloindolines and furoindolines via cascade dearomatization of indole derivatives with carbenium ion. Chemical communications (Cambridge, England), 2015, Apr-07, Volume: 51, Issue:27 A highly efficient intermolecular cascade dearomatization of substituted indoles with benzodithiolylium tetrafluoroborate has been developed. This reaction provides a novel strategy to synthesise C3 methyl-substituted pyrroloindolines and furoindolines under mild reaction conditions, the utility of which has been demonstrated by the synthesis of esermethol and physovenine in a highly concise manner. Topics: Borates; Catalysis; Furans; Indoles; Molecular Structure; Physostigmine; Pyrroles; Stereoisomerism	2015
Unified Approach to the Spiro(pyrrolidinyl-oxindole) and Hexahydropyrrolo[2,3-b]indole Alkaloids: Total Syntheses of Pseudophrynamines 270 and 272A. Organic letters, 2015, Dec-04, Volume: 17, Issue:23 The first enantioselective total syntheses of architecturally interesting prenylated pyrroloindole alkaloids, (-)-pseudophrynamines 272A (3d) and 270 (3b), have been achieved starting from enantioenriched 2-oxindoles having all-carbon quaternary stereocenters. A common strategy involving a thio-urea catalyzed aldol reaction is employed for the total synthesis of both spiro(pyrrolidinyl-oxindole) and hexahydropyrrolo[2,3-b]indole alkaloids. Topics: Aldehydes; Aniline Compounds; Catalysis; Indole Alkaloids; Indoles; Molecular Structure; Oxindoles; Physostigmine; Prenylation; Spiro Compounds; Stereoisomerism	2015

Article

Year

Synthesis of pyrroloindolines and furoindolines via cascade dearomatization of indole derivatives with carbenium ion.

Chemical communications (Cambridge, England), 2015, Apr-07, Volume: 51, Issue:27

A highly efficient intermolecular cascade dearomatization of substituted indoles with benzodithiolylium tetrafluoroborate has been developed. This reaction provides a novel strategy to synthesise C3 methyl-substituted pyrroloindolines and furoindolines under mild reaction conditions, the utility of which has been demonstrated by the synthesis of esermethol and physovenine in a highly concise manner.

Topics: Borates; Catalysis; Furans; Indoles; Molecular Structure; Physostigmine; Pyrroles; Stereoisomerism

2015

Unified Approach to the Spiro(pyrrolidinyl-oxindole) and Hexahydropyrrolo[2,3-b]indole Alkaloids: Total Syntheses of Pseudophrynamines 270 and 272A.

Organic letters, 2015, Dec-04, Volume: 17, Issue:23

The first enantioselective total syntheses of architecturally interesting prenylated pyrroloindole alkaloids, (-)-pseudophrynamines 272A (3d) and 270 (3b), have been achieved starting from enantioenriched 2-oxindoles having all-carbon quaternary stereocenters. A common strategy involving a thio-urea catalyzed aldol reaction is employed for the total synthesis of both spiro(pyrrolidinyl-oxindole) and hexahydropyrrolo[2,3-b]indole alkaloids.

Topics: Aldehydes; Aniline Compounds; Catalysis; Indole Alkaloids; Indoles; Molecular Structure; Oxindoles; Physostigmine; Prenylation; Spiro Compounds; Stereoisomerism

2015