Efficient synthesis of 2,6,9-triazabicyclo[3.3.1]nonanes through amine-mediated formal [4+4] reaction of unsaturated imines-Reference-Cited by-同舟云学术

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Efficient synthesis of 2,6,9-triazabicyclo[3.3.1]nonanes through amine-mediated formal [4+4] reaction of unsaturated imines

Published:2012-10 Issue:44 Volume:53 Page:5899-5902
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Tanaka Katsunori,Siwu Eric R.O.,Hirosaki Shinji,Iwata Takayuki,Matsumoto Risa,Kitagawa Yasutaka,Pradipta Ambara R.,Okumura Mitsutaka,Fukase Koichi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference34 articles.

1. New strategy in synthetic biology: from enzyme inhibition and natural products synthesis to PET imaging by 6π-azaelectrocyclization

2. Exploring a Unique Reactivity of 6π-Azaelectrocyclization to Enzyme Inhibition, Natural Products Synthesis, and Molecular Imaging: An Approach to Chemical Biology by Synthetic Chemists

3. Novel Synthesis of the Ocular Age Pigment A2-E: New Method for Substituted Pyridine Synthesis via Azaelectrocyclization

4. Significant Acceleration of 6π-Azaelectrocyclization Resulting from a Remarkable Substituent Effect and Formal Synthesis of the Ocular Age Pigment A2-E by a New Method for Substituted Pyridine Synthesis

5. Highly Stereoselective Asymmetric 6π-Azaelectrocyclization Utilizing the Novel 7-Alkyl Substituted cis-1-Amino-2-indanols: Formal Synthesis of 20-Epiuleine

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1. SYNTHESIS OF TWO PYRROLIDINE-2,5-DIONE DERIVATIVES AS ANTIBACTERIAL AGENTS;HETEROCYCL LETT;2022

2. Application of Acrolein Imines to Organic Synthesis, Biofunctional Studies, and Clinical Practice;The Chemical Record;2021-03-26

3. Enantioselective synthesis of cyclic and linear diamines by imine cycloadditions;Chirality;2020-07-03

4. Selectfluor-Mediated Stereoselective [1 + 1 + 4 + 4] Dimerization of Styrylnaphthols;Organic Letters;2019-12-10

5. Facile Assembling of Novel 2,3,6,7,9-pentaazabicyclo- [3.3.1]nona-3,7-diene Derivatives under Microwave and Ultrasound Platforms;Molecules;2019-03-20

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