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  Asymmetric Catalysis via Cyclic, Aliphatic Oxocarbenium Ions

Lee, S., Kaib, P. S., & List, B. (2017). Asymmetric Catalysis via Cyclic, Aliphatic Oxocarbenium Ions. Journal of the American Chemical Society, 139(6), 2156-2159. doi:10.1021/jacs.6b11993.

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Lee, Kaib, List 2017.pdf (Postprint), 836KB
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Lee, Kaib, List 2017.pdf
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 Creators:
Lee, Sunggi1, Author           
Kaib, Philip S.J.1, Author           
List, Benjamin1, Author           
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1Research Department List, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445585              

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 Abstract: A direct enantioselective synthesis of substituted oxygen heterocycles from lactol acetates and enolsilanes has been realized using a highly reactive and confined imidodiphosphorimidate (IDPi) catalyst. Various chiral oxygen heterocycles, including tetrahydrofurans, tetrahydropyrans, oxepanes, chromans, and dihydrobenzofurans, were obtained in excellent enantioselectivities by reacting the corresponding lactol acetates with diverse enol silanes. Mechanistic studies suggest the reaction to proceed via a nonstabilized, aliphatic, cyclic oxocarbenium ion intermediate paired with the confined chiral counteranion.

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Language(s): eng - English
 Dates: 2016-11-212017-02-072017-02-15
 Publication Status: Issued
 Pages: 4
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1021/jacs.6b11993
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Title: Journal of the American Chemical Society
  Other : J. Am. Chem. Soc.
  Abbreviation : JACS
Source Genre: Journal
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Publ. Info: Washington, DC : American Chemical Society
Pages: - Volume / Issue: 139 (6) Sequence Number: - Start / End Page: 2156 - 2159 Identifier: ISSN: 0002-7863
CoNE: https://pure.mpg.de/cone/journals/resource/954925376870