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  Protective group tuning in the stereoselective conversion of α-amino aldehydes into aminoalkyl epoxides

Reetz, M. T., & Binder, J. (1989). Protective group tuning in the stereoselective conversion of α-amino aldehydes into aminoalkyl epoxides. Tetrahedron Letters, 30(40), 5425-5428. doi:10.1016/S0040-4039(01)80584-0.

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Item Permalink: https://hdl.handle.net/21.11116/0000-000E-7CEA-0 Version Permalink: https://hdl.handle.net/21.11116/0000-000E-7CEB-F
Genre: Journal Article

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 Creators:
Reetz, M. T.1, Author           
Binder, J.1, Author
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1Philipps-Universität Marburg, Fachbereich Chemie, Hans-Meerwein-Straße, Marburg, ou_persistent22              

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 Abstract: Sulfonium and arsonium ylides of the type CH2=S(CH3)2 and CH2=As(Ph)3 react with doubly protected α-amino aldehydes 1 derived from amino acids to form aminoalkyl epoxides 3/4, diastereofacial selectivity ranging between 86:14 and 95:5.

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Language(s): eng - English
 Dates: 1989-08-081989
 Publication Status: Issued
 Pages: 4
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1016/S0040-4039(01)80584-0
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Title: Tetrahedron Letters
  Abbreviation : Tetrahedron Lett.
Source Genre: Journal
 Creator(s):
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Publ. Info: Oxford : Pergamon
Pages: - Volume / Issue: 30 (40) Sequence Number: - Start / End Page: 5425 - 5428 Identifier: ISSN: 0040-4039
CoNE: https://pure.mpg.de/cone/journals/resource/954925448772