Dearomatization of 3‐Nitroindoles with Highly γ‐Functionalized Allenoates in Formal (3+2) Cycloadditions-Reference-Cited by-同舟云学术

Dearomatization of 3‐Nitroindoles with Highly γ‐Functionalized Allenoates in Formal (3+2) Cycloadditions

Published:2019-09-30 Issue:60 Volume:25 Page:13688-13693
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Birbaum Léo¹,Gillard Laurent¹,Gérard Hélène²^ORCID,Oulyadi Hassan¹^ORCID,Vincent Guillaume³^ORCID,Moreau Xavier⁴^ORCID,De Paolis Michael¹^ORCID,Chataigner Isabelle¹²^ORCID

Affiliation:

1. UNIROUENINSA RouenCNRSCOBRANormandie Univ 76000 Rouen France

2. CNRSLaboratoire de Chimie ThéoriqueLCT UMR7616Sorbonne Université 75005 Paris France

3. Institut de Chimie Moléculaire et des Matériaux d'Orsay (ICMMO)Univ. Paris-Sud, Université Paris-Saclay, CNRS UMR 8182 91405 Orsay cedex France

4. Institut Lavoisier VersaillesUMR CNRS 8180Université de Versailles-St-Quentin-en-Yvelines, Université Paris Saclay 78035 Versailles cedex France

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.201903455

Reference68 articles.

1. Nucleophilic Dearomatizing (DNAr) Reactions of Aromatic C,H-Systems. A Mature Paradigm in Organic Synthesis

2. Reactions of Nucleophiles with Nitroarenes: Multifacial and Versatile Electrophiles

3. Benzofurans as Efficient Dienophiles in Normal Electron Demand [4 + 2] Cycloadditions

4. For nitro-indoles -pyrroles or -naphthalenes involved as dienophiles in Diels–Alder cycloadditions see for instance:

5. Five-membered aromatic heterocycles as dienophiles in Diels-Alder reactions. Furan, pyrrole, and indole

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