Synthesis of β-Lactams from Diazoketones and Imines: The Use of Microwave Irradiation-Reference-Cited by-同舟云学术

Synthesis of β-Lactams from Diazoketones and Imines: The Use of Microwave Irradiation

Published:2001-05-12 Issue:12 Volume:3 Page:1849-1851
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Linder Michael R.¹,Podlech Joachim¹

Affiliation:

1. Institut für Organische Chemie der Universität Stuttgart, Pfaffenwaldring 55, D-70569 Stuttgart, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol015891%2B

Reference40 articles.

1. Stereoselective Synthesis of Aminoalkyl-Substituted β-Lactams via Cycloaddition of Ketenes Generated from α-Amino Acids

2. Cycloadditions of Ketenes Generated in the Wolff Rearrangement. Stereoselective Synthesis of Aminoalkyl-Substituted β-Lactams from α-Amino Acids

3. A Chiral, Oxidatively Cleavable Auxiliary in β-Lactam Synthesis - Double Diastereocontrol with p-Methoxyphenethyl-Substituted Imines

4. (d) Podlech, J.; Linder, M. R. InBioorganic ChemistryHighlights and New Aspects; Diederichsen, U., Lindhorst, T. K., Westermann, B., Wessjohann, L., Eds.; Wiley-VCH: Weinheim, 1999; p 43.

5. Synthesis of Peptidomimetics Containing a β-Lactam Moiety Using Peptidic Diazoketones and Imines in a Staudinger Reaction

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