Stereoselective synthesis of α,γ-diamino-β-hydroxy amino acid esters: A new 
class of amino acids

Reetz, M. T.; Wünsch, T.; Harms, K.

doi:10.1016/0957-4166(90)90036-A

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Stereoselective synthesis of α,γ-diamino-β-hydroxy amino acid esters: A new class of amino acids

Reetz, M. T., Wünsch, T., & Harms, K. (1990). Stereoselective synthesis of α,γ-diamino-β-hydroxy amino acid esters: A new class of amino acids. Tetrahedron: Asymmetry, 1(6), 371-374. doi:10.1016/0957-4166(90)90036-A.

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Item Permalink: https://hdl.handle.net/21.11116/0000-000E-7CD1-B Version Permalink: https://hdl.handle.net/21.11116/0000-000E-7CD2-A

Genre: Journal Article

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Creators:
Reetz, M. T.¹, Author
Wünsch, T.¹, Author
Harms, K.¹, Author

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1Philipps-Universität Marburg, Fachbereich Chemie, Hans-Meerwein-Straße, Marburg, ou_persistent22

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Abstract: Isocyano-acetic acid ethylester 3 undergoes a base catalyzed aldol-type addition to N,N-dibenzylamino aldehydes 6 to form oxazolines 7 stereoselectively; these can be ring-opened with NEt₃, affording α,γ-diamino-β-hydroxy amino acid esters 2 .

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Language(s): eng - English

Dates: Submitted: 1190-05-15Date issued: 1990

Publication Status: Issued

Pages: 4

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Rev. Type: Peer

Identifiers: DOI: 10.1016/0957-4166(90)90036-A

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Title: Tetrahedron: Asymmetry

Source Genre: Journal

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Publ. Info: Oxford : Pergamon

Pages: - Volume / Issue: 1 (6) Sequence Number: - Start / End Page: 371 - 374 Identifier: ISSN: 0957-4166
CoNE: https://pure.mpg.de/cone/journals/resource/954925577039