Synthesis of 2-Spiropseudoindoxyls via an Intramolecular Nitroalkyne Redox–Dipolar Cycloaddition Cascade-Reference-Cited by-同舟云学术

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Synthesis of 2-Spiropseudoindoxyls via an Intramolecular Nitroalkyne Redox–Dipolar Cycloaddition Cascade

Published:2014-12-29 Issue:2 Volume:17 Page:270-273
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Marien Niels¹,Brigou Ben,Pinter Balazs,De Proft Frank,Verniest Guido¹

Affiliation:

1. Research Group of Organic Chemistry, Department of Chemistry and Department of Bio-Engineering Sciences, Faculty of Science and Bio-Engineering Sciences, and ‡Research Group of General Chemistry, Vrije Universiteit Brussel (VUB), Pleinlaan 2, B-1050 Brussels, Belgium

Funder

Vrije Universiteit Brussel

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol503364w

Reference48 articles.

1. A chemical synthesis of 11-methoxy mitragynine pseudoindoxyl featuring the interrupted Ugi reaction

2. New Strategies for the Synthesis of Monoterpene Indole Alkaloids

3. A Short Synthetic Route to (+)-Austamide, (+)-Deoxyisoaustamide, and (+)-Hydratoaustamide from a Common Precursor by a Novel Palladium-Mediated Indole → Dihydroindoloazocine Cyclization

4. Strategies for the enantioselective synthesis of spirooxindoles

5. Spiroindolones, a Potent Compound Class for the Treatment of Malaria

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4. dppb and TfOH promoted cascade reaction of o-nitrophenylpropiolamides to access C2-spiro-pseudoindoxyls;Organic Chemistry Frontiers;2024

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