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  Chelation-Controlled Stereoselective Synthesis of Cyanohydrins

Reetz, M. T., Kesseler, K., & Jung, A. (1985). Chelation-Controlled Stereoselective Synthesis of Cyanohydrins. Angewandte Chemie, International Edition in English, 24(11), 989-991. doi:10.1002/anie.198509891.

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Item Permalink: https://hdl.handle.net/21.11116/0000-000E-7E79-E Version Permalink: https://hdl.handle.net/21.11116/0000-000E-A367-6
Genre: Journal Article

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 Creators:
Reetz, Manfred T.1, Author           
Kesseler, Kurt1, Author
Jung, Alfred1, Author
Affiliations:
1Philipps-Universität Marburg, Fachbereich Chemie, Hans-Meerwein-Straße, Marburg, ou_persistent22              

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 Abstract: Tertiary and secondary alkoxycyanohydrins such as 1 and 2 can be synthesized in high diasteromeric purity. Alkoxyacyl cyanides are allowed to react with allylsilanes or alkoxyaldehydes with silyl cyanides, namely in the presence of chelating reagents such as TiCl4, SnCl4, or Znl2.

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Language(s): eng - English
 Dates: 1985-07-111985-11-01
 Publication Status: Issued
 Pages: 3
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1002/anie.198509891
 Degree: -

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Title: Angewandte Chemie, International Edition in English
  Abbreviation : Angew. Chem., Int. Ed. Engl.
Source Genre: Journal
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Publ. Info: Weinheim : Wiley-VCH
Pages: - Volume / Issue: 24 (11) Sequence Number: - Start / End Page: 989 - 991 Identifier: ISSN: 0570-0833
CoNE: https://pure.mpg.de/cone/journals/resource/0570-0833