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Perturbation theory model of reactivity and enantioselectivity of palladium-catalyzed Heck–Heck cascade reactions

RSC advances, 2016-01, Vol.6 (45), p.38602-38610

2016

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Enantioselective synthesis in organic and medicinal chemistry

Current topics in medicinal chemistry, 2014, Vol.14 (10), p.1209

2014

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Tandem Parham cyclisation––α-amidoalkylation reaction in the synthesis of the isoindolo[1,2- a ]isoquinoline skeleton of nuevamine-type alkaloids

Tetrahedron letters, 2004-02, Vol.45 (6), p.1253-1256

2004

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An efficient entry to pyrrolo[1,2- b]isoquinolines and related systems through Parham cyclisation

Tetrahedron, 2005-03, Vol.61 (13), p.3311-3324

2005

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Enantiodivergent Synthesis of Pyrrolo[2,1-a]isoquinolines Based on Diastereoselective Parham Cyclization and α-Amidoalkylation Reactions

Journal of organic chemistry, 2004-05, Vol.69 (11), p.3875-3885

2004

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Parham-Type Cycliacylation with Weinreb Amides. Application to the Synthesis of Fused Indolizinone Systems

Organic letters, 2003-04, Vol.5 (7), p.1115-1117

2003

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Perturbation theory model of reactivity and enantioselectivity of palladium-catalyzed Heck-Heck cascade reactionsElectronic supplementary information (ESI) available. See DOI: 10.1039/c6ra08751e

2016-04

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ChemInform Abstract: Carbolithiation of Carbon-Carbon Multiple Bonds

ChemInform, 2012-09, Vol.43 (36), p.no-no

2012

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Bischler-Napieralski Reaction of C2′, Functionalized 1,2-Diarylethylamides: A General Approach to the Synthesis of Protoberberines

Synlett, 1993, Vol.1993 (6), p.431-433

1993

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A practical approach to the fused β-carboline system. Asymmetric synthesis of indolo[2,3- a]indolizidinones via a diastereoselective intramolecular α-amidoalkylation reaction

Tetrahedron letters, 2003-11, Vol.44 (46), p.8445-8448

2003

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Highly Diastereoselective Intramolecular α-Amidoalkylation Reactions of Hydroxylactams Derived from N-Phenethylimides. Enantioselective Synthesis of Dihydropyrrolo[2,1-a] isoquinolones

Synlett, 2002, Vol.2002 (4), p.593-597

2002

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Synthesis of enantiomerically enriched amines by chiral ligand mediated addition of organolithium reagents to imines

Tetrahedron: asymmetry, 2001-08, Vol.12 (14), p.2077-2082

2001

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Knowledge Updates 2011/4

1st Edition., 2012

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Bischler-Napieralski Cyclization-N/C-Alkylation Sequences for the Construction of Isoquinoline Alkaloids. Synthesis of Protoberberines and Benzo[c]phenanthridines via C-2'-Functionalized 3-Arylisoquinolines(1)

Journal of organic chemistry, 1996-06, Vol.61 (12), p.4062-4072

1996

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Metalation vs Nucleophilic Addition in the Reactions of N-Phenethylimides with Organolithium Reagents. Ready Access to Isoquinoline Derivatives via N-Acyliminium Ions and Parham-Type Cyclizations

Journal of organic chemistry, 1997-04, Vol.62 (7), p.2080-2092

1997

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Stereodivergent Synthesis of Hetero-Fused Isoquinolines by Acyliminium and Metallation Methods

European journal of organic chemistry, 2001-04, Vol.2001 (7), p.1267-1277

2001

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Enantioselective synthesis of pyrrolo[2,1- a]isoquinolones via stereocontrolled N-acyliminium ion cyclisations

Tetrahedron letters, 2001-02, Vol.42 (8), p.1511-1513

2001

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Synthesis of enantiomerically enriched β-amino alcohol derivatives via asymmetric lithiation of O-benzyl carbamates–imine addition using (−)-sparteine complexes

Tetrahedron: asymmetry, 2002-03, Vol.13 (3), p.311-316

2002

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Functionalized organolithium compounds: Generation via reductive lithiation and nucleophilic addition to N-phenethylimides. Access to functionalized dihydropyrrolo[2,1- a]isoquinolinones

Tetrahedron, 1998-10, Vol.54 (40), p.12361-12378

1998

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Metalation–cyclisation sequence on N-( o-halobenzyl)pyrroles. Synthesis of pyrrolo[1,2- b]isoquinolones

Tetrahedron letters, 2000-07, Vol.41 (27), p.5211-5214

2000

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Tandem carbophilic addition- N-acyliminium ion cyclization for the synthesis of functionalized pyrrolo[2,1-a]isoquinolones: Key intermediates for the preparation of Erythrina-type alkaloids

Tetrahedron letters, 1996-10, Vol.37 (43), p.7841-7844

1996

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Diastereodivergent Approaches to Thiazolo[4,3-a]isoquinoline Systems via Parham-type and N-acyliminium ion Cyclizations

Synlett, 2000, Vol.2000 (1), p.101-103

2000

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Parham-type cyclization and nucleophilic addition - N-acyliminium ion cyclization sequences for the construction of the isoquinoline nucleus

Tetrahedron letters, 1996-08, Vol.37 (34), p.6193-6196

1996

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Diastereoselective Conjugate Addition of α-Lithiodithioacetals to the α,β-Unsaturated Lactam Unit of 5,6-Dihydropyrrolo[2,1-a]isoquinolinones

Synlett, 1999-09, Vol.1999 (9), p.1486-1488

1999

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Isoquinoline formation via iminium ions cyclization: A direct approach to c-2′ functionalized 3-aryltetrahydroisoquinolines

Tetrahedron, 1995-10, Vol.51 (44), p.12159-12168

1995

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Perturbation theory model of reactivity and enantioselectivity of palladium-catalyzed Heck–Heck cascade reactions

Enantioselective synthesis in organic and medicinal chemistry

Tandem Parham cyclisation––α-amidoalkylation reaction in the synthesis of the isoindolo[1,2- a ]isoquinoline skeleton of nuevamine-type alkaloids

An efficient entry to pyrrolo[1,2- b]isoquinolines and related systems through Parham cyclisation

Enantiodivergent Synthesis of Pyrrolo[2,1-a]isoquinolines Based on Diastereoselective Parham Cyclization and α-Amidoalkylation Reactions

Parham-Type Cycliacylation with Weinreb Amides. Application to the Synthesis of Fused Indolizinone Systems

Perturbation theory model of reactivity and enantioselectivity of palladium-catalyzed Heck-Heck cascade reactionsElectronic supplementary information (ESI) available. See DOI: 10.1039/c6ra08751e

ChemInform Abstract: Carbolithiation of Carbon-Carbon Multiple Bonds

Bischler-Napieralski Reaction of C2′, Functionalized 1,2-Diarylethylamides: A General Approach to the Synthesis of Protoberberines

A practical approach to the fused β-carboline system. Asymmetric synthesis of indolo[2,3- a]indolizidinones via a diastereoselective intramolecular α-amidoalkylation reaction

Highly Diastereoselective Intramolecular α-Amidoalkylation Reactions of Hydroxylactams Derived from N-Phenethylimides. Enantioselective Synthesis of Dihydropyrrolo[2,1-a] isoquinolones

Synthesis of enantiomerically enriched amines by chiral ligand mediated addition of organolithium reagents to imines

Knowledge Updates 2011/4

Bischler-Napieralski Cyclization-N/C-Alkylation Sequences for the Construction of Isoquinoline Alkaloids. Synthesis of Protoberberines and Benzo[c]phenanthridines via C-2'-Functionalized 3-Arylisoquinolines(1)

Metalation vs Nucleophilic Addition in the Reactions of N-Phenethylimides with Organolithium Reagents. Ready Access to Isoquinoline Derivatives via N-Acyliminium Ions and Parham-Type Cyclizations

Stereodivergent Synthesis of Hetero-Fused Isoquinolines by Acyliminium and Metallation Methods

Enantioselective synthesis of pyrrolo[2,1- a]isoquinolones via stereocontrolled N-acyliminium ion cyclisations

Synthesis of enantiomerically enriched β-amino alcohol derivatives via asymmetric lithiation of O-benzyl carbamates–imine addition using (−)-sparteine complexes

Functionalized organolithium compounds: Generation via reductive lithiation and nucleophilic addition to N-phenethylimides. Access to functionalized dihydropyrrolo[2,1- a]isoquinolinones

Metalation–cyclisation sequence on N-( o-halobenzyl)pyrroles. Synthesis of pyrrolo[1,2- b]isoquinolones

Tandem carbophilic addition- N-acyliminium ion cyclization for the synthesis of functionalized pyrrolo[2,1-a]isoquinolones: Key intermediates for the preparation of Erythrina-type alkaloids

Diastereodivergent Approaches to Thiazolo[4,3-a]isoquinoline Systems via Parham-type and N-acyliminium ion Cyclizations

Parham-type cyclization and nucleophilic addition - N-acyliminium ion cyclization sequences for the construction of the isoquinoline nucleus

Diastereoselective Conjugate Addition of α-Lithiodithioacetals to the α,β-Unsaturated Lactam Unit of 5,6-Dihydropyrrolo[2,1-a]isoquinolinones

Isoquinoline formation via iminium ions cyclization: A direct approach to c-2′ functionalized 3-aryltetrahydroisoquinolines

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