The Wonderful Chemistry of Trifluoromethyl α-Haloalkenyl Ketones-Reference-Cited by-同舟云学术

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The Wonderful Chemistry of Trifluoromethyl α-Haloalkenyl Ketones

Published:2018-05-07 Issue:27-28 Volume:2018 Page:3609-3617
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Rulev Alexander Yu.¹^ORCID

Affiliation:

1. A. E. Favorsky Institute of Chemistry; Siberian Division of the Russian Academy of Sciences; 664033 Irkutsk Russia

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference33 articles.

1. Haloalkenes activated by geminal groups in reactions with N-nucleophiles

2. CXXXIV.—Acetylenic ketones

3. Serendipity or the art of making discoveries

4. Studies of the π-electron distribution in push-pull alkenes by1H and13C NMR spectroscopy—II

5. Stereoelectronic structure of α-bromoalkenyl trifluoromethyl ketones

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3. Nucleophilic reactions of ethyl (Z)-2‑bromo-4,4,4-trifluorobut-2-enoate: One molecule – various heterocycles;Journal of Fluorine Chemistry;2022-02

4. Synthesis of 1‐Trifluoromethylated Propargyl Alcohols by Two Successive Reactions of Cyclopentylmagnesium Bromide in a One‐Pot Manner;Asian Journal of Organic Chemistry;2022-01-04

5. Expanding 1,2,4-triketone toolbox for use as fluorinated building blocks in the synthesis of pyrazoles, pyridazinones and β-diketohydrazones;Journal of Fluorine Chemistry;2022-01

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