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  Synthesis of Carbohydrate Derived α-Methylene-γ-lactones by Diasterecseldctive, Low Temperature Reformatsky-Type Reactions

Csuk, R., Fürstner, A., Sterk, H., & Weidmann, H. (1986). Synthesis of Carbohydrate Derived α-Methylene-γ-lactones by Diasterecseldctive, Low Temperature Reformatsky-Type Reactions. Journal of Carbohydrate Chemistry, 5(3), 459-467. doi:10.1080/07328308608058849.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-000F-F18E-B Version Permalink: https://hdl.handle.net/21.11116/0000-0008-564A-5
Genre: Journal Article

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 Creators:
Csuk, René1, Author
Fürstner, Alois1, Author           
Sterk, Heinz2, Author
Weidmann, Hans1, Author
Affiliations:
1Institute of Organic Chemistry, Technical University Graz, A-8010 Graz, Austria, ou_persistent22              
2Institute of Organic Chemistry, Karl-Franzens-University, 8010 Graz, Austria, ou_persistent22              

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 Abstract: Hexopyranoside- and hexofuranose uloses with either ethyl 2-(branamethyl)acrylate in the presence of laminar Zn/Ag-graphite or ethyl 2-(trimethylsilylinethyl)acrylate/tetra-n-butylanrnonium fluoride undergo stereoselective branching, mainly with formation of spiro α-methylene-γ-lactones.

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Language(s): eng - English
 Dates: 1986-01-231986-06-131986
 Publication Status: Issued
 Pages: 9
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1080/07328308608058849
 Degree: -

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Title: Journal of Carbohydrate Chemistry
  Abbreviation : J. Carbohydr. Chem.
Source Genre: Journal
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Publ. Info: Philadelphia, PA USA : Taylor & Francis
Pages: - Volume / Issue: 5 (3) Sequence Number: - Start / End Page: 459 - 467 Identifier: ISSN: 0732-8303
ISSN: 1532-2327
CoNE: https://pure.mpg.de/cone/journals/resource/0732-8303