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1-Amino- and 1,3-Diaminoimidazolium Salts

✍ Scribed by Dr. Helmut Link; Prof. Dr. Wilhelm Klötzer; Dr. Eva Maria Karpitschka; Dr. Marc Montavon; Dr. Renate Müssner; Dr. Nicolas Singewald


Publisher
John Wiley and Sons
Year
1990
Tongue
English
Weight
251 KB
Volume
29
Category
Article
ISSN
0044-8249

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✦ Synopsis


The configuration of the alkylation products (e.g., 6 and 7) are fully in accord with this analysis.

In summary, chiral auxiliary compounds (3) of a new shape have been described, and their action can be related to the stereoelectronics of enolate alkylations. The asymmetric environment of the auxiliary compounds is so well defined in structures such as 3b that such materials show efficiency as asymmetric protonation agents.


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