Conjugated Nitrodienes. Synthesis and Reactivity-Reference-Cited by-同舟云学术

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Conjugated Nitrodienes. Synthesis and Reactivity

Published:2013-01-11 Issue:5 Volume:113 Page:3493-3515
ISSN:0009-2665
Container-title:Chemical Reviews
language:en
Short-container-title:Chem. Rev.

Author:

Ballini Roberto¹,Araújo Noelia²,Gil María V.³,Román Emilio³,Serrano José A.³

Affiliation:

1. School of Science and Technology, Chemistry Division, via S. Agostino 1, I-62032 Camerino, Italy

2. Chemistry Research Laboratory, University of Oxford, Mansfield Road, Oxford OX1 3TA, United Kingdom

3. Departamento de Química Orgánica e Inorgánica, Facultad de Ciencias, Universidad de Extremadura, 06071 Badajoz, Spain

Publisher

American Chemical Society (ACS)

Subject

General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/cr2002195

Reference179 articles.

1. Facile cycloaddition of 2-phenylsulfonyl 1,3-dienes to indoles

2. Synthesis of 2-nitro 1,3-dienes. Useful intermediates in the preparation of unsaturated 1,4-dicarbonyl compounds

3. Dimerization of (e)-2-benzenesulfonyl-1,3-alkadienes the benzenesulfonyl group exerts acyclic stereocontrol

4. The Use of Sulfonyl 1,3-Dienes in Organic Synthesis

5. Asymmetric Diels–Alder reactions between chiral sugar nitroalkenes and 1-O-substituted buta-1,3-dienes. Synthesis and reactivity of new cyclohexenyl derivatives

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1. (1E,3E)-1,4-Dinitro-1,3-butadiene—Synthesis, Spectral Characteristics and Computational Study Based on MEDT, ADME and PASS Simulation;Molecules;2024-01-22

2. Useful 1,2-dioxygenated dienes: syntheses and Diels–Alder reactions en route to substituted 2-naphthols and phenols;Organic Chemistry Frontiers;2024

3. Radical Cascade Cyclization of 1,n-Enynes, 1,n-Diynes, 1,n-Enallenes, 1,n-Yneallenes, and 1,n-Bisallenes;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2024

4. Recent Developments in Photocatalytic Reduction of Nitro Compounds to Valuable Scaffolds;Synlett;2023-07-04

5. Recent advances in the chemistry of two-carbon nitro-containing synthetic equivalents;Успехи химии;2023-04

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