Ugi reaction-derived 1H-pyrrol-2(5H)-ones proved as valid precursors to a new class of heterocyclic α-diazocarbonyl compounds-Reference-Cited by-同舟云学术

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Ugi reaction-derived 1H-pyrrol-2(5H)-ones proved as valid precursors to a new class of heterocyclic α-diazocarbonyl compounds

Published:2022-01 Issue: Volume:89 Page:153598
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Budeev Anton,Kantin Grigory,Dar'in Dmitry,Krasavin Mikhail

Funder

Russian Foundation for Basic Research

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference23 articles.

1. Cyclic diazo compounds in the construction of spirocyclic scaffolds

2. https://www.reaxys.com

3. Synthesis of Spiro[indazole-3,3′-indolin]-2′-ones via [3 + 2] Dipolar Cycloaddition of Arynes with 3-Diazoindolin-2-ones and Indazolo[2,3-c]quinazolin-6(5H)-ones by Subsequent Thermal Isomerization

4. Diastereoselective synthesis of macrocycles incorporating the spiro-indolofurans and -indolodioxolanes

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1. Propiolic Acids in the Synthesis of N-heterocycles;Mini-Reviews in Organic Chemistry;2023-11

2. Regioselective Construction of Indolylated Cyclic Tetrasubstituted Carbon Centers through Brønsted Acid‐Catalyzed Dearomative Skeletal Rearrangement of Azofurans;Advanced Synthesis & Catalysis;2023-09-29

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