Efficient Synthesis of Furan-2-ylacetates, 7-(Alkoxycarbonyl)benzofurans, and 7-(Alkoxycarbonyl)-2,3-dihydrobenzofurans Based on Cyclization Reactions of Free and Masked Dianions: A “Cyclization/Dehydrogenation” Strategy-Reference-Cited by-同舟云学术

Efficient Synthesis of Furan-2-ylacetates, 7-(Alkoxycarbonyl)benzofurans, and 7-(Alkoxycarbonyl)-2,3-dihydrobenzofurans Based on Cyclization Reactions of Free and Masked Dianions: A “Cyclization/Dehydrogenation” Strategy

Published:2005-10-19 Issue:24 Volume:70 Page:10013-10029
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, 18059 Rostock, Germany, Institut für Chemie und Biochemie, Universität Greifswald, Soldmannstr. 16, 17487 Greifswald, Germany, and Leibniz-Institut für Organische Katalyse an der Universität Rostock e. V. (IfOK), Albert-Einstein-Str. 29a, 18059 Rostock, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo051767i

Reference44 articles.

1. A mild method for the synthesis of furans. Application to 2,5-bridged furano macrocyclic compounds

2. Synthesis of furans by silver(I)-promoted cyclization of allenyl ketones and aldehydes

3. Synthesis of 2,5-furanocycles through intraannular cyclization of macrocyclic allenones

4. Synthesis of rosefuran. A new route to furans through base-catalyzed cyclization of hydroxy alkynoates and alkynones

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