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  A Tunable and Enantioselective Hetero-Diels-Alder Reaction Provides Access to Distinct Piperidinoyl Spirooxindoles

Jayakumar, S., Louven, K., Strohmann, C., & Kumar, K. (2017). A Tunable and Enantioselective Hetero-Diels-Alder Reaction Provides Access to Distinct Piperidinoyl Spirooxindoles. Angewandte Chemie International Edition, 56(50), 15945-15949. doi:10.1002/anie.201708355.

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Item Permalink: https://hdl.handle.net/21.11116/0000-0000-6306-A Version Permalink: https://hdl.handle.net/21.11116/0000-0000-6307-9
Genre: Journal Article

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 Creators:
Jayakumar, Samydurai1, Author           
Louven, Kathrin2, Author
Strohmann, Carsten2, Author
Kumar, Kamal1, Author           
Affiliations:
1Abt. IV: Chemische Biologie, Max Planck Institute of Molecular Physiology, Max Planck Society, ou_1753290              
2External Organizations, ou_persistent22              

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Free keywords: asymmetric synthesis; azadienes; cycloaddition; heterocycles; spiro-compounds
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Language(s): eng - English
 Dates: 2017-12
 Publication Status: Issued
 Pages: -
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 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1002/anie.201708355
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Title: Angewandte Chemie International Edition
  Other : Angew. Chem., Int. Ed.
  Other : Angew. Chem. Int. Ed.
  Other : Angewandte Chemie, International Edition
Source Genre: Journal
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Publ. Info: Weinheim : Wiley-VCH
Pages: - Volume / Issue: 56 (50) Sequence Number: - Start / End Page: 15945 - 15949 Identifier: ISSN: 1433-7851
CoNE: https://pure.mpg.de/cone/journals/resource/1433-7851