Convenient Synthesis of ε-Halo-β-ketoesters and γ,γ‘-Dibromoalkanones by Regio- and Chemoselective Reaction of 2-Alkylidenetetrahydrofurans with Boron Trihalides: A “Ring-Closure/Ring-Cleavage” Strategy-Reference-Cited by-同舟云学术

Convenient Synthesis of ε-Halo-β-ketoesters and γ,γ‘-Dibromoalkanones by Regio- and Chemoselective Reaction of 2-Alkylidenetetrahydrofurans with Boron Trihalides: A “Ring-Closure/Ring-Cleavage” Strategy

Published:2005-04-07 Issue:10 Volume:70 Page:3819-3825
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Bellur Esen¹,Langer Peter¹

Affiliation:

1. Institut für Chemie, Universität Rostock, Albert-Einstein-Str. 3a, 18051 Rostock, Germany, and Institut für Chemie und Biochemie, Universität Greifswald, Soldmannstr. 16, 17487 Greifswald, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo047824%2B

Reference22 articles.

1. A FACILE SYNTHESIS OF 1,3-DICARBONYL COMPOUNDS FROM 1-ALKYNE AND ACID ANHYDRIDE PROMOTED BY DICHLORO-BIS(TRIFLUOROMETHANESULFONATO)TITANIUM(IV)

2. Synthesis of single isomers (E or Z) of protected γ,δ-unsaturated ketones by the Horner-Wittig reaction

3. Enantiospecific synthesis of acromelic acid A via a cobalt-mediated cyclisation reaction

4. An unexpected product in the photooxygenation of a cyclic enol ether

5. Application of the intramolecular aza-Wittig reaction to the synthesis of vinylogous urethanes and amides

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