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Literature DB >> 18081292

Alpha-amination of nitrogen heterocycles: ring-fused aminals.

Chen Zhang¹, Chandra Kanta De, Rudrajit Mal, Daniel Seidel.

Abstract

Entities: Chemical

Mesh：

Substances：

Year: 2008 PMID： 18081292 DOI： 10.1021/ja077473r

Source DB: PubMed Journal: J Am Chem Soc ISSN： 0002-7863 Impact factor: 15.419

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42 in total

1. Multicomponent assembly strategies for the synthesis of diverse tetrahydroisoquinoline scaffolds.

Authors: Brett A Granger; Kyosuke Kaneda; Stephen F Martin
Journal: Org Lett Date: 2011-08-11 Impact factor: 6.005

2. Redox-Annulations of Cyclic Amines with ortho-Cyanomethylbenzaldehydes.

Authors: Anirudra Paul; Hemant S Chandak; Longle Ma; Daniel Seidel
Journal: Org Lett Date: 2020-01-27 Impact factor: 6.005

3. Synthesis of Cyclic α-Aminophosphonates through Copper Catalyzed Enamine Activation.

Authors: Junbin Han; Robert S Paton; Bo Xu; Gerald B Hammond
Journal: Synthesis (Stuttg) Date: 2013-02-01 Impact factor: 3.157

4. A facile, metal- and solvent-free, autoxidative coupling of quinolines with indoles and pyrroles.

Authors: Mikaël Brasse; Jonathan A Ellman; Robert G Bergman
Journal: Chem Commun (Camb) Date: 2011-03-29 Impact factor: 6.222

5. Facile Access to Ring-Fused Aminals via Direct α-Amination of Secondary Amines with ortho-Aminobenzaldehydes. Synthesis of Vasicine, Deoxyvasicine, Deoxyvasicinone, Mackinazolinone and Ruteacarpine.

Authors: Matthew T Richers; Indubhusan Deb; Alena Yu Platonova; Chen Zhang; Daniel Seidel
Journal: Synthesis (Stuttg) Date: 2013-10-06 Impact factor: 3.157

Alpha-amination of nitrogen heterocycles: ring-fused aminals.

1. Multicomponent assembly strategies for the synthesis of diverse tetrahydroisoquinoline scaffolds.

2. Redox-Annulations of Cyclic Amines with ortho-Cyanomethylbenzaldehydes.

3. Synthesis of Cyclic α-Aminophosphonates through Copper Catalyzed Enamine Activation.

4. A facile, metal- and solvent-free, autoxidative coupling of quinolines with indoles and pyrroles.

5. Facile Access to Ring-Fused Aminals via Direct α-Amination of Secondary Amines with ortho-Aminobenzaldehydes. Synthesis of Vasicine, Deoxyvasicine, Deoxyvasicinone, Mackinazolinone and Ruteacarpine.

6. Redox-Annulations of Cyclic Amines with Electron-Deficient o-Tolualdehydes.

7. Redox-neutral α-arylation of amines.

8. Redox-neutral copper(II) carboxylate catalyzed α-alkynylation of amines.

9. Formation of N-alkylpyrroles via intermolecular redox amination.

10. Intramolecular Redox-Mannich Reactions: Facile Access to the Tetrahydroprotoberberine Core.