Starting from three achiral compounds, the title reaction provides rapid access to a variety of molecules that contain indoline, tetrahydroquinoline, and tetrahydroisoquinoline moieties (see scheme). The process features the efficient formation of multiple new bonds and chiral centers, excellent stereoselectivity, oxetane desymmetrization, and easy product purification through filtration. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
A mild and efficient stereoselective synthesis of hexacyclic indole alkaloids with a tetrahydro-β-ca...
An enantioselective total synthesis of (-)-terengganensine A, a heptacyclic monoterpene indole alkal...
This thesis explores the applications of organocatalysis and its combination with metal catalysis fo...
ABSTRACT: A mild and efficient stereoselective synthesis of hexacyclic indole alkaloids with a tetra...
Ru-catalyzed tandem amine oxidative dehydrogenation/formal aza-Diels–Alder reaction for enanti...
Expanding upon the recently developed aminocatalytic asymmetric indole-2,3-quinodimethane strategy, ...
The electrophilic reactivity of a series of novel pyrazole-4,5-dione derivatives in the organocataly...
Tetracyclic indolines are ubiquitous skeletons in bioactive natural products and pharmaceuticals, an...
Tetracyclic indolines are ubiquitous skeletons in bioactive natural products and pharmaceuticals, an...
Tetracyclic indolines are ubiquitous skeletons in bioactive natural products and pharmaceuticals, an...
Tetracyclic indolines are ubiquitous skeletons in bioactive natural products and pharmaceuticals, an...
The thesis embodies the results of studies on “Synthesis of polynuclear azaheterocycles based on ind...
A mild and efficient stereoselective synthesis of hexacyclic indole alkaloids with a tetrahydro-β-ca...
Cycloaddition reactions are powerful transformations for the construction of various cyclic organic ...
This thesis explores the applications of organocatalysis and its combination with metal catalysis fo...
A mild and efficient stereoselective synthesis of hexacyclic indole alkaloids with a tetrahydro-β-ca...
An enantioselective total synthesis of (-)-terengganensine A, a heptacyclic monoterpene indole alkal...
This thesis explores the applications of organocatalysis and its combination with metal catalysis fo...
ABSTRACT: A mild and efficient stereoselective synthesis of hexacyclic indole alkaloids with a tetra...
Ru-catalyzed tandem amine oxidative dehydrogenation/formal aza-Diels–Alder reaction for enanti...
Expanding upon the recently developed aminocatalytic asymmetric indole-2,3-quinodimethane strategy, ...
The electrophilic reactivity of a series of novel pyrazole-4,5-dione derivatives in the organocataly...
Tetracyclic indolines are ubiquitous skeletons in bioactive natural products and pharmaceuticals, an...
Tetracyclic indolines are ubiquitous skeletons in bioactive natural products and pharmaceuticals, an...
Tetracyclic indolines are ubiquitous skeletons in bioactive natural products and pharmaceuticals, an...
Tetracyclic indolines are ubiquitous skeletons in bioactive natural products and pharmaceuticals, an...
The thesis embodies the results of studies on “Synthesis of polynuclear azaheterocycles based on ind...
A mild and efficient stereoselective synthesis of hexacyclic indole alkaloids with a tetrahydro-β-ca...
Cycloaddition reactions are powerful transformations for the construction of various cyclic organic ...
This thesis explores the applications of organocatalysis and its combination with metal catalysis fo...
A mild and efficient stereoselective synthesis of hexacyclic indole alkaloids with a tetrahydro-β-ca...
An enantioselective total synthesis of (-)-terengganensine A, a heptacyclic monoterpene indole alkal...
This thesis explores the applications of organocatalysis and its combination with metal catalysis fo...