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Meijere, Armin

Submitted by Armin de Meijere, Harald Winsel, and Bjorn Stecker1. [Pg.9]

Prof. Dr. Armin de Meijere Institut fiir Organische Chemie Georg-August-Universitat TammannstraCe 2 D-37077 Gottingen, Germany E-mail ameijerl uni-goettingen.de... [Pg.233]

Armin de Meijere, Sergei I. Kozhushkov, and Andrei I. Savchenko n.i... [Pg.390]

Armin de Meijere, Gottingen Kendall N. Houk, Los Angeles Jean-Marie Lehn, Strasbourg Steven V. Ley, Cambridge, UK... [Pg.190]

Armin de Meijere Sergei I. Kozhushkov Alexander R Khlebnikov... [Pg.89]

Less than two years after Chan and I disclosed the synthesis of 72 and 73, a more practical synthesis of 72 based on palladium-mediated reactions was reported by Armin de Meijere. I was deeply impressed by the highly efficient way Armin and his co-worker, Oliver Reiser, were preparing 72 as well as its derivatives. Immediately, I realized that it was impractical to compete with them. I therefore quit the dibenzo[2.2]paracyclophane field, with the strong conviction that many other unknown theoretically interesting molecules were still waiting for our pursuit. [Pg.125]

Prof. Dr. Armin De Meijere Universitat Hamburg Institut f. Org. Chemie u. Biochemie Martin-Luther-King-Platz 6 D-2000 Hamburg 13... [Pg.164]

See other pages where Meijere, Armin is mentioned: [Pg.143]    [Pg.397]    [Pg.143]    [Pg.397]    [Pg.21]    [Pg.264]    [Pg.280]    [Pg.206]    [Pg.233]    [Pg.234]    [Pg.5]    [Pg.5]    [Pg.5]    [Pg.8]    [Pg.6]    [Pg.532]    [Pg.3]    [Pg.6]    [Pg.5]    [Pg.6]    [Pg.166]    [Pg.275]    [Pg.237]    [Pg.271]    [Pg.200]    [Pg.296]    [Pg.245]    [Pg.467]    [Pg.232]    [Pg.234]    [Pg.234]    [Pg.236]    [Pg.238]    [Pg.320]    [Pg.206]    [Pg.251]   
See also in sourсe #XX -- [ Pg.272 ]



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Armin de Meijere and Oliver Reiser 11 Palladium-Catalyzed Carbozincation

Meijer

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Rainer Haag and Armin de Meijere Abstract

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