Radical Nitration-Debromination of α-Bromo-α-fluoroalkenes as a Stereoselective Route to Aromatic α-Fluoronitroalkenes—Functionalized Fluorinated Building Blocks for Organic Synthesis-Reference-Cited by-同舟云学术

Radical Nitration-Debromination of α-Bromo-α-fluoroalkenes as a Stereoselective Route to Aromatic α-Fluoronitroalkenes—Functionalized Fluorinated Building Blocks for Organic Synthesis

Published:2017-05-10 Issue:10 Volume:82 Page:5274-5284
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Motornov Vladimir A.¹²,Muzalevskiy Vasiliy M.³,Tabolin Andrey A.¹^ORCID,Novikov Roman A.¹⁴,Nelyubina Yulia V.⁵^ORCID,Nenajdenko Valentine G.³,Ioffe Sema L.¹

Affiliation:

1. N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky prosp. 47, Moscow 119991, Russian Federation

2. Higher Chemical College, D. I. Mendeleev University of Chemical Technology of Russia, Miusskaya sq. 9, Moscow 125047, Russian Federation

3. Department of Chemistry, M. V. Lomonosov Moscow State University, Leninskie Gory 1, Moscow 119992, Russian Federation

4. V. A. Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Vavilov str. 32, Moscow 119991, Russian Federation

5. A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, Vavilov str. 28, Moscow 119991, Russian Federation

Funder

Russian Science Foundation

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.7b00578

Reference95 articles.

1. Stereoselective reactions of nitro compounds in the synthesis of natural compound analogs and active pharmaceutical ingredients

2. Secondary Amines as Lewis Bases in Nitroalkene Activation

3. Morita-Baylis-Hillman and Rauhut-Currier Reactions of Conjugated Nitroalkenes

4. Some Aspects of the Chemistry of Nitro Compounds

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