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  Metal-catalyzed rearrangement of enantiomerically pure alkylidenecyclopropane derivatives as a new access to cyclobutenes possessing quaternary stereocenters

Masarwa, A., Fürstner, A., & Marek, I. (2009). Metal-catalyzed rearrangement of enantiomerically pure alkylidenecyclopropane derivatives as a new access to cyclobutenes possessing quaternary stereocenters. Chemical Communications, (38), 5760-5762. doi:10.1039/B910465H.

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Item Permalink: http://hdl.handle.net/11858/00-001M-0000-000F-8F31-F Version Permalink: http://hdl.handle.net/11858/00-001M-0000-0025-BC08-C
Genre: Journal Article

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 Creators:
Masarwa, Ahmad1, Author
Fürstner, Alois1, Author              
Marek, Ilan2, Author
Affiliations:
1The Mallat Family Laboratory of Organic Chemistry, Schulich Faculty of Chemistry and the Lise Meitner-Minerva Center for Computational Quantum Chemistry, Technion-Israel Institute of Technology, Haifa 32000, Israel, ou_persistent22              
2Research Department Fürstner, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445584              

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 Abstract: Pd(II)- and Pt(II)-catalyzed ring-expansion of enantiomerically pure alkylidenecyclopropane derivatives leads to the formation of cyclobutene species with a complete preservation of the stereogenic center.

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Language(s): eng - English
 Dates: 2009-05-282009-08-072009-09-022009-10-14
 Publication Status: Published in print
 Pages: 3
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 460836
DOI: 10.1039/B910465H
ISI: 000270115300028
 Degree: -

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Title: Chemical Communications
  Other : Chem. Commun.
Source Genre: Journal
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Publ. Info: Cambridge, UK : Royal Society of Chemistry
Pages: - Volume / Issue: (38) Sequence Number: - Start / End Page: 5760 - 5762 Identifier: ISSN: 1359-7345
CoNE: https://pure.mpg.de/cone/journals/resource/954928495413