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Synthesis of Tetracyclic C2-Symmetric Ketiminium Salts and Evaluation as Catalysts for Epoxidation

ORGANIC LETTERS (2023)

Unraveling the C2-Symmetric Azatetraquinane System. Simple, Enantioselective Syntheses

G. Sudhakar Reddy et al.

Summary: A concise stereocontrolled synthetic route to the C-2-symmetric azatetraquinane 1 (or its enantiomer) has been described, involving innovation in methodology for [3+2] cycloaddition and stereochemical control.

ORGANIC LETTERS (2021)

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Article Chemistry, Organic

Recent Advances in Iminium-Salt-Catalysed Asymmetric Epoxidation

David P. Day et al.

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY (2017)

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Article Chemistry, Organic

New biphenyl iminium salt catalysts for highly enantioselective asymmetric epoxidation: role of additional substitution and dihedral angle

Philip C. Bulman Page et al.

ORGANIC & BIOMOLECULAR CHEMISTRY (2016)

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Review Chemistry, Multidisciplinary

Iminium catalysis

Anniina Erkkila et al.

CHEMICAL REVIEWS (2007)

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Article Chemistry, Medicinal

Dopamine/serotonin receptor ligands.: 10:: SAR studies on azecine-type dopamine receptor Ligands by functional screening at human cloned D1, D2L, and D5 receptors with a microplate reader based calcium assay lead to a novel potent D1/D5 selective antagonist

B Hoefgen et al.

JOURNAL OF MEDICINAL CHEMISTRY (2006)

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Article Chemistry, Multidisciplinary

Copper-catalyzed domino halide exchange-cyanation of aryl bromides

J Zanon et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2003)

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Synthesis of Tetracyclic C2-Symmetric Ketiminium Salts and Evaluation as Catalysts for Epoxidation

相关参考文献

Unraveling the C2-Symmetric Azatetraquinane System. Simple, Enantioselective Syntheses

Recent Advances in Iminium-Salt-Catalysed Asymmetric Epoxidation

New biphenyl iminium salt catalysts for highly enantioselective asymmetric epoxidation: role of additional substitution and dihedral angle

Iminium catalysis

Dopamine/serotonin receptor ligands.: 10:: SAR studies on azecine-type dopamine receptor Ligands by functional screening at human cloned D1, D2L, and D5 receptors with a microplate reader based calcium assay lead to a novel potent D1/D5 selective antagonist

Copper-catalyzed domino halide exchange-cyanation of aryl bromides

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